Crystallography Open Database

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7132518 CIFC130 H162 K2 Mg2 N4 O4C 1 2/c 158.863; 9.9267; 34.1523
90; 144.652; 90
11545Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132519 CIFC49 H68 N2 OP -113.0578; 13.4792; 13.9769
67.548; 70.378; 81.771
2141.24Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132520 CIFC118 H178 K2 Mg2 N4 O4P b c a19.617; 21.324; 25.718
90; 90; 90
10758Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132521 CIFC43 H45 N8 O8.5P 1 21/n 115.804; 30.856; 21.944
90; 101.44; 90
10488Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132522 CIFC49 H44 N8 O8P -4 n 223.5856; 23.5856; 7.525
90; 90; 90
4186Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132523 CIFC49 H44 N8 O8I 1 2/a 113.879; 12.595; 27.719
90; 102.35; 90
4733Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132524 CIFC49 H44 N8 O8I 1 2/a 111.6434; 16.4405; 26.1717
90; 96.002; 90
4982.4Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132525 CIFC49 H60 N8 O16P -113.6429; 15.3717; 16.0809
62.706; 89.94; 63.745
2600.16Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132526 CIFC13 H15 Br N2 O4C 1 2/c 119.5005; 7.9603; 18.992
90; 110.951; 90
2753.2Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132527 CIFC13 H13 Br N2 O3P 1 21/c 110.5757; 12.8565; 10.0965
90; 111.417; 90
1277.99Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132528 CIFC10 H15 Br N2 O3 SP 1 21/c 17.8851; 16.802; 10.6416
90; 111.647; 90
1310.4Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132529 CIFC24 H24 N4 O4P 1 21 18.7417; 13.759; 9.4773
90; 112.031; 90
1056.67Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132530 CIFC12 H10 N2 O3P 1 21/c 112.1802; 11.8247; 14.6931
90; 90.067; 90
2116.2Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132531 CIFC20 H8 N6 Se2 TeP 63/m m c21.656; 21.656; 7.6612
90; 90; 120
3111.6Eckstein, Brian J.; Martin, Hannah R.; Moghadasnia, Michael P.; Halder, Arijit; Melville, Michael J.; Buzinski, Tara N.; Balaich, Gary J.; McGuirk, C. Michael
Influence of donor point modifications on the assembly of chalcogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 758-761
7132532 CIFC20 H8 N6 Se2 TeC 1 2/c 112.505; 36.9389; 7.7404
90; 107.994; 90
3400.57Eckstein, Brian J.; Martin, Hannah R.; Moghadasnia, Michael P.; Halder, Arijit; Melville, Michael J.; Buzinski, Tara N.; Balaich, Gary J.; McGuirk, C. Michael
Influence of donor point modifications on the assembly of chalcogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 758-761
7132533 CIFC20 H8 N6 Se2 TeP 63/m m c21.529; 21.529; 7.653
90; 90; 120
3071.9Eckstein, Brian J.; Martin, Hannah R.; Moghadasnia, Michael P.; Halder, Arijit; Melville, Michael J.; Buzinski, Tara N.; Balaich, Gary J.; McGuirk, C. Michael
Influence of donor point modifications on the assembly of chalcogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 758-761
7132534 CIFC37 H31 Cl8 Ga N2 P2P c a 2142.402; 11.4012; 16.4543
90; 90; 90
7954.6Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132535 CIFC76 H70 Cl8 Ga2 N10 O P4P -19.9147; 18.9028; 23.475
68.039; 85.656; 76.81
3972.5Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132536 CIFC44 H51 Cl4 Ga N2 O2 P2P -111.2788; 13.1565; 16.1265
95.445; 108.409; 91.577
2256.1Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132537 CIFC41 H45 Cl6 Ga N2 O4 P2P 19.792; 10.064; 12.02
96.899; 93.763; 95.349
1167.3Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132538 CIFC43 H33.5 Cl4 F2 Ga N3 P2P 1 n 112.1657; 18.5693; 19.1345
90; 102.701; 90
4216.9Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132539 CIFC78 H140 Al2 K2 N4 O10 Si4P 1 21 115.7613; 13.63024; 21.2238
90; 89.397; 90
4559.3O'Reilly, Andrea; Gardiner, Michael G.; McMullin, Claire L.; Fulton, J. Robin; Coles, Martyn P.
Aluminyl derived ethene functionalization with heteroallenes, leading to an intramolecular ligand rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 881-884
7132540 CIFC116 H170 Al2 K2 N8 O2 Si4P 1 21/c 113.45606; 23.22737; 19.4534
90; 108.146; 90
5777.75O'Reilly, Andrea; Gardiner, Michael G.; McMullin, Claire L.; Fulton, J. Robin; Coles, Martyn P.
Aluminyl derived ethene functionalization with heteroallenes, leading to an intramolecular ligand rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 881-884
7132541 CIFC85 H146 Al2 K2 N8 O3 Si4P 1 21/c 121.7767; 16.40993; 25.5079
90; 98.7193; 90
9010.01O'Reilly, Andrea; Gardiner, Michael G.; McMullin, Claire L.; Fulton, J. Robin; Coles, Martyn P.
Aluminyl derived ethene functionalization with heteroallenes, leading to an intramolecular ligand rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 881-884
7132542 CIFC118 H89 B2 F8 N19 Pd2P 1 21 114.567; 22.094; 18.901
90; 105.02; 90
5875Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132543 CIFC36 H28 Cl4 N4P 1 21/n 113.1218; 7.9693; 15.0239
90; 98.834; 90
1552.44Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132544 CIFC29.5 H24 Cl3 N4C 1 2 126.38; 7.7267; 12.814
90; 98.307; 90
2584.5Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132545 CIFC204 H144 B6 F24 N24 Pd3P -116.7748; 28.6322; 29.6738
110.451; 94.927; 100.329
12965.9Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132546 CIFC18 H16 Br N O2 S2P b c n18.3295; 10.5061; 18.8191
90; 90; 90
3624.02Chen, Xi; Li, Rui-Peng; Long, Peng; Tang, Yuxi; Li, Jia; Tang, Shouchu
Indium-catalyzed inter- and intramolecular dithianyl-alkyne metathesis reactions.
Chemical communications (Cambridge, England), 2024, 60, 1285-1288
7132547 CIFC61 H61 Cl0.08 F0.92 N6 ThP 1 21/c 116.63492; 11.85014; 24.83906
90; 90.9154; 90
4895.8Mangel, Daniel N.; Brewster, James T.; Juarez, Gabriel J.; Lynch, Vincent M.; Sessler, Jonathan L.
Cyclopentadienyl capped thorium(IV) porphyrinoid complex.
Chemical communications (Cambridge, England), 2024, 60, 1020-1022
7132548 CIFC78 H82 N6 O6 ThP -114.3339; 14.7275; 17.9016
92.412; 90.923; 117.468
3347.4Mangel, Daniel N.; Brewster, James T.; Juarez, Gabriel J.; Lynch, Vincent M.; Sessler, Jonathan L.
Cyclopentadienyl capped thorium(IV) porphyrinoid complex.
Chemical communications (Cambridge, England), 2024, 60, 1020-1022
7132549 CIFC19 H14 N O P SP -18.385; 10.473; 10.511
109.339; 92.044; 102.717
843.7Sun, Guangping; Li, Menghang; Cai, Lijuan; Zhu, Jinli; Tang, Yanfeng; Yao, Yong
Carbazole-based artificial light-harvesting system for photocatalytic cross-coupling dehydrogenation reaction.
Chemical communications (Cambridge, England), 2024, 60, 1412-1415
7132550 CIFC296 H122 Ag27 Au34 F68 PP -121.0215; 22.1806; 35.4832
88.101; 74.928; 87.324
15954.4Deng, Guocheng; Ki, Taeyoung; Liu, Xiaolin; Chen, Yuping; Lee, Kangjae; Yoo, Seungwoo; Tang, Qing; Bootharaju, Megalamane S.; Hyeon, Taeghwan
Tailoring the subshell and electronic structure of an atomically precise AuAg alloy nanocluster.
Chemical communications (Cambridge, England), 2024, 60, 1289-1292
7132551 CIFC62 H62 N14 O18 S2P -18.6132; 14.1366; 15.1958
103.568; 105.921; 102.22
1652.5Zhang, Xin; Mao, Lijun; He, Rongjing; Shi, Yanting; Li, Lingyi; Li, Shuo; Zhu, Chenghao; Zhang, Yanjing; Ma, Da
Tunable cyclic operation of dissipative molecular switches based on anion recognition.
Chemical communications (Cambridge, England), 2024, 60, 1180-1183
7132552 CIFC44 H68 B10 N4 S2 Si2P -113.3084; 13.6054; 16.2398
76.297; 82.378; 61.662
2513.7Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132553 CIFC48 H64 B10 F6 N6 O3 Si2P 1 21/c 114.118; 18.777; 20.911
90; 99.975; 90
5460Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132554 CIFC40 H63 B10 N5 O3 Si2P 1 21/n 112.922; 17.399; 21.674
90; 104.21; 90
4724Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132555 CIFC64 H88.54 B10 N6 O2 S2 Si2P -111.741; 17.4714; 18.7329
112.618; 101.299; 100.144
3341.5Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132556 CIFC62 H87 B10 N6 O3 Si2P 1 21/n 112.2822; 20.2269; 25.5456
90; 90.955; 90
6345.4Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132557 CIFC14 H20 B10P 1 21/c 115.8355; 10.979; 9.9081
90; 100.451; 90
1694Yang, Han-Bo; Guo, Yan; Cao, Ke; Jiang, Qi-Jia; Teng, Chao-Chao; Zhu, Dao-Yong; Wang, Shao-Hua
Iridium-catalyzed selective arylation of B(6)-H of 3-aryl-<i>o</i>-carboranes with arylboronic acid <i>via</i> direct B-H activation.
Chemical communications (Cambridge, England), 2024, 60, 1124-1127
7132558 CIFC61 H74 O10 S4C 1 2/c 121.59; 20.575; 13.578
90; 97.516; 90
5979.7Zhao, Xueru; Hua, Bin; Shao, Li
Constructing a solid-state supramolecular polymer based on host-guest recognition between perethylated pillar[5]arene and tetrathiafulvalene.
Chemical communications (Cambridge, England), 2024, 60, 1164-1167
7132559 CIFC14 H14 Cd O2 S2P -16.8847; 8.411; 12.8724
92.96; 101.422; 105.459
699.89Nishibe, Asuka; Akiyoshi, Ryohei; Saeki, Akinori; Ogasawara, Kazuyoshi; Tsuruoka, Takaaki; Tanaka, Daisuke
Engineering of CdS-chain arrays assembled through S⋯S interactions in 1D semiconductive coordination polymers.
Chemical communications (Cambridge, England), 2024, 60, 1277-1280
7132560 CIFC14 H14 Cd O2 S2I b a 235.4228; 16.8199; 7.2761
90; 90; 90
4335.2Nishibe, Asuka; Akiyoshi, Ryohei; Saeki, Akinori; Ogasawara, Kazuyoshi; Tsuruoka, Takaaki; Tanaka, Daisuke
Engineering of CdS-chain arrays assembled through S⋯S interactions in 1D semiconductive coordination polymers.
Chemical communications (Cambridge, England), 2024, 60, 1277-1280
7132561 CIFC14 H14 Cd O2 S2P c c n28.1725; 13.9425; 7.0402
90; 90; 90
2765.36Nishibe, Asuka; Akiyoshi, Ryohei; Saeki, Akinori; Ogasawara, Kazuyoshi; Tsuruoka, Takaaki; Tanaka, Daisuke
Engineering of CdS-chain arrays assembled through S⋯S interactions in 1D semiconductive coordination polymers.
Chemical communications (Cambridge, England), 2024, 60, 1277-1280
7132562 CIFC76 Cl28C 1 2/c 117.137; 23.973; 15.008
90; 90.389; 90
6165.5Brotsman, Victor A.; Troyanov, Sergey I.
Non-classical (NC), heptagon-containing fullerenes obtained <i>via</i> chlorination-promoted cage transformations: C<sub>76</sub>(NC2a)Cl<sub>24</sub> and C<sub>76</sub>(NC2b)Cl<sub>28</sub>.
Chemical communications (Cambridge, England), 2024, 60, 893-896
7132563 CIFC83 H8 Cl24C 1 2/c 123.672; 21.259; 16.433
90; 131.763; 90
6168.5Brotsman, Victor A.; Troyanov, Sergey I.
Non-classical (NC), heptagon-containing fullerenes obtained <i>via</i> chlorination-promoted cage transformations: C<sub>76</sub>(NC2a)Cl<sub>24</sub> and C<sub>76</sub>(NC2b)Cl<sub>28</sub>.
Chemical communications (Cambridge, England), 2024, 60, 893-896
7132564 CIFC34 H21 F6 N OP c a 2127.071; 13.5223; 7.5005
90; 90; 90
2745.6Barhate, Komal Vasant; Wadawale, Amey P.; Chandrakumar, K. R. S.; Agarwal, Neeraj
Modulation of Δ<i>E</i><sub>ST</sub> and room temperature phosphorescence in carbazole derivatives.
Chemical communications (Cambridge, England), 2024, 60, 1408-1411
7132565 CIFC32 H21 F2 N OP 1 21/c 114.5446; 21.9876; 7.5051
90; 101.383; 90
2352.93Barhate, Komal Vasant; Wadawale, Amey P.; Chandrakumar, K. R. S.; Agarwal, Neeraj
Modulation of Δ<i>E</i><sub>ST</sub> and room temperature phosphorescence in carbazole derivatives.
Chemical communications (Cambridge, England), 2024, 60, 1408-1411
7132566 CIFC57 H74.5 Br2.94 Cl1.06 Mg N5.5 O4 Zn2P -113.4199; 20.874; 23.345
96.6727; 97.517; 107.576
6096.2Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132567 CIFC108.92 H138.37 Br2.52 Cl0.48 Mg3 N10.46 O10 Zn3P n m a28.44051; 33.62784; 12.56775
90; 90; 90
12019.7Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132568 CIFC200 H259 Mg5 N7 O20 Zn2P -117.175; 23.5379; 25.6364
89.281; 73.491; 87.287
9925.5Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132569 CIFC112.37 H147.56 Br3.42 Cl0.58 Mg2 N9.19 O10 Zn4P 1 21/c 119.81378; 25.56149; 24.42596
90; 108.387; 90
11739.5Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132570 CIFC36 H29 N O3 SP 1 21/c 118.5043; 8.0564; 18.619
90; 103.185; 90
2702.5Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132571 CIFC21 H23 N O3 SP 21 21 2110.2093; 12.452; 14.4031
90; 90; 90
1831.01Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132572 CIFC23 H25 N O4 SP 1 21/n 110.2361; 18.336; 10.7234
90; 98.878; 90
1988.6Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132573 CIFC25 H23 N O3 SP 1 21/n 110.9271; 16.5749; 10.9904
90; 93.352; 90
1987.1Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132574 CIFC26 H31 N O4P 21 21 217.5575; 12.6622; 25.9109
90; 90; 90
2479.5Xie, Xiang-Qi; Li, Xingguang; Liu, Pei-Nian
Enantioselective synthesis of spiro-<i>N</i>,<i>O</i>-ketals <i>via</i> iridium and Brønsted acid co-catalyzed asymmetric formal [4+2] cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 1448-1451
7132575 CIFC26 H31 N O4P 21 21 218.9352; 9.9706; 26.0378
90; 90; 90
2319.7Xie, Xiang-Qi; Li, Xingguang; Liu, Pei-Nian
Enantioselective synthesis of spiro-<i>N</i>,<i>O</i>-ketals <i>via</i> iridium and Brønsted acid co-catalyzed asymmetric formal [4+2] cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 1448-1451
7132576 CIFC50.56 H53.12 N6 O4.28P 6518.9446; 18.9446; 22.0233
90; 90; 120
6845.2Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132577 CIFC48 H46 N6 O5P 21 21 2116.082; 17.555; 17.564
90; 90; 90
4959Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132578 CIFC56 H64 N6 O7P -111.244; 12.917; 17.778
86.525; 87.331; 75.394
2492.7Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132579 CIFC106 H110 Cl18 F6 N12 O20 S2 ZnP -116.0885; 20.1668; 21.6212
103.611; 101.577; 109.328
6129.8Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132580 CIFC19 H17 N3 SP 1 21/c 17.7135; 22.94; 9.6284
90; 100.29; 90
1676.3Zhang, Xiaoxiang; Liu, Chenrui; Wei, Wanxing; Zhang, Zhuan; Liang, Taoyuan
Iodine-dependent oxidative regioselective aminochalcogenation of indolines.
Chemical communications (Cambridge, England), 2024, 60, 1152-1155
7132581 CIFC25 H26 O5P -110.1019; 10.718; 11.1905
64.873; 69.562; 83.168
1027.3Wu, Shu-Yi; Li, Yang; Shen, Peng; Yang, Xin-Han; Ran, Guang-Yao
Palladium-catalysed fragmentary esterification-induced allylic alkylation of allyl carbonates and cyclic vinylogous anhydrides.
Chemical communications (Cambridge, England), 2024, 60, 1416-1419
7132582 CIFC25 H21 Co F O4 PC 1 2/c 120.3694; 11.8516; 19.7496
90; 106.855; 90
4562.9Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132583 CIFC22 H33 Co F O4 PP n m a16.5748; 13.6875; 10.2341
90; 90; 90
2321.79Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132584 CIFC16 H27 Co F O4 PP b c a14.9882; 15.8456; 16.4634
90; 90; 90
3910Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132585 CIFC116 H128 N8 O24 S8P 1 21/c 115.6273; 11.1454; 21.3411
90; 104.896; 90
3592.1Ho, An T.; Vanable, Evan P.; Miguel, Chelsea San; Hull, Kami L.
Iridium-catalysed hydroamination of internal homoallylic amines.
Chemical communications (Cambridge, England), 2024, 60, 1615-1618
7132586 CIFC31 H42 N2 O7 S2P 21 21 2111.1123; 11.2096; 24.9678
90; 90; 90
3110.1Ho, An T.; Vanable, Evan P.; Miguel, Chelsea San; Hull, Kami L.
Iridium-catalysed hydroamination of internal homoallylic amines.
Chemical communications (Cambridge, England), 2024, 60, 1615-1618
7132587 CIFC25.5 H31 Cl N5C 1 2/c 129.863; 9.4396; 17.2974
90; 101.266; 90
4782.1Mohanty, Aisa; Rout, Smruti Rekha; Dandela, Rambabu; Daw, Prosenjit
Ammonia synthesis by the reductive N-N bond cleavage of hydrazine using an air-stable, phosphine-free ruthenium catalyst.
Chemical communications (Cambridge, England), 2024, 60, 416-419
7132588 CIFC14 H19 N O6P c a 2117.469; 7.599; 11.007
90; 90; 90
1461.1Zheng, Peng Xuan; Ou, Song Lin; Qu, Lei Yu; Zhang, Ying; Jiang, Shi Qing; Li, Xiang; Wan, Jun Xiong; Zhang, Min; Bao, Xin
Enriched switching in a donor-acceptor Stenhouse adduct <i>via</i> reversible covalent bonding.
Chemical communications (Cambridge, England), 2024, 60, 1333-1336
7132589 CIFC151.5 H201 Au14 Cl F3 P4.5 S9P -115.8928; 20.0176; 29.1486
75.045; 78.775; 78.621
8681.3Liu, Dong; Gao, Guiqi; Zhang, Yongyu; Li, Qinzhen; Yang, Sha; Chai, Jinsong; Yu, Haizhu; Zhu, Manzhou
[Au<sub>14</sub>(2-SAdm)<sub>9</sub>(Dppe)<sub>2</sub>]<sup>+</sup>: a gold nanocluster with a crystallization-induced emission enhancement phenomenon.
Chemical communications (Cambridge, England), 2024, 60, 1337-1340
7132590 CIFC24 H21 N3 O3 SP -18.0853; 10.9301; 13.3531
104.791; 92.638; 111.152
1051.52Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132591 CIFC24 H20 Br3 N3 O3 SP -110.8989; 11.4714; 11.6523
66.814; 72.69; 71.71
1246Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132592 CIFC26 H25 N3 O4 SP 21 21 2110.5361; 17.81; 26.2442
90; 90; 90
4924.67Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132593 CIFC96 H72 Ag24 N48 O24F d d 245.975; 37.787; 3.754
90; 90; 90
6521.7Peng, Shuyin; Sun, Yuqian; Li, Qingqing; Jiang, Zhongwen; Rao, Yin; Wu, Yichen; Li, Qiaowei
Stepwise construction of coordinative linkages and dynamic covalent linkages for a porous metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 1488-1491
7132594 CIFC27 H30 N2 O3 SP 21 21 219.7941; 11.2385; 23.348
90; 90; 90
2569.9Cui, Chen-Chang; Lin, Feng; Wang, Lu-Yao; Liu, Yin-Ping; Tu, Shu-Jiang; Tu, Man-Su; Hao, Wen-Juan; Jiang, Bo
Olefin skeletal rearrangement enabling access to multiarylated <i>N</i>-sulfonyl amidines.
Chemical communications (Cambridge, England), 2024, 60, 1492-1495
7132595 CIFC24 H22 I2 N4 O4 SP 14.7109; 5.1887; 25.0379
84.32; 88.126; 87.821
608.31Cao, Jinlian; Weng, Peimin; Qi, Yuanwei; Lin, Kexin; Yan, Xiaosheng
Noncovalent interaction network of chalcogen, halogen and hydrogen bonds for supramolecular β-sheet organization.
Chemical communications (Cambridge, England), 2024, 60, 1484-1487
7132596 CIFC73 H55 Cl3 N6 O3P c a 2124.6915; 14.7339; 15.6091
90; 90; 90
5678.6Chen, Lihua; Li, Chenfei; Liu, Zheng-Fei; Kuboi, Yoshiaki; Fu, Enguang; Vargas, Lydia Sosa; Adachi, Chihaya; Mathevet, Fabrice; Zhang, Shaodong
A donor-acceptor cage for circularly polarized TADF emission.
Chemical communications (Cambridge, England), 2024, 60, 1758-1761
7132597 CIFC60 H82 B3 K N6 OC 1 2/c 125.1162; 13.2745; 18.3072
90; 110.891; 90
5702.5Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132598 CIFC67 H86 B3 Br N6 O2 SiP 1 21 111.4979; 20.9867; 13.7765
90; 104.384; 90
3220.1Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132599 CIFC54 H76 B3 Br N6P 1 21/c 113.321; 20.663; 19.283
90; 100.62; 90
5217Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132600 CIFC108 H152 B6 Cl6 N12 O2 Si2P 21 21 2119.4723; 23.1794; 24.8889
90; 90; 90
11233.8Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132601 CIFC61.5 H83.5 B3 Cl Ge N6 OP -116.4864; 16.4582; 44.137
95.16; 97.087; 89.93
11835.7Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132602 CIFC108 H152 B6 Br6 N12 O2 Si2P 21 21 2119.5876; 23.2994; 24.9438
90; 90; 90
11383.8Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132603 CIFC162 H228 B9 Cl3 N18 O3 Sn3P 1 21/n 130.8728; 16.2163; 33.9145
90; 106.314; 90
16295.4Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132604 CIFC23 H22 N2P 1 21/c 110.8961; 18.4187; 9.4952
90; 111.962; 90
1767.3Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132605 CIFC22 H19 F N2P 1 21/c 110.454; 20.0412; 9.0834
90; 106.374; 90
1825.9Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132606 CIFC22 H20 N2P 1 21/c 110.0309; 19.6236; 9.0074
90; 104.371; 90
1717.6Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132607 CIFC23 H20 N2 OP -17.4394; 10.1901; 13.5234
98.505; 92.733; 110.436
944.63Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132608 CIFC44 H43 Cl2 N3 O6 SP -18.7541; 15.3319; 15.5807
82.471; 85.577; 81.058
2044.53Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132609 CIFC48 H43 Cl O P2 PdC 1 2/m 119.3124; 18.4281; 12.7741
90; 103.027; 90
4429.2Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132610 CIFC49 H41 F3 O4 P2 Pd SP 1 21/m 19.2641; 18.7713; 12.8967
90; 101.38; 90
2198.6Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132611 CIFC4 H6 N8 O2P n a 216.744; 11.212; 9.487
90; 90; 90
717.3Kumar, Parasar; Kumar, Navaneet; Ghule, Vikas D.; Dharavath, Srinivas
Zwitterionic fused pyrazolo-triazole based high performing energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 1646-1649
7132612 CIFC52 H50 N2 O4C 1 2/c 119.961; 14.527; 16.049
90; 118.68; 90
4082.8Gentile, Giuseppe; Bartolomei, Beatrice; Dosso, Jacopo; Demitri, Nicola; Filippini, Giacomo; Prato, Maurizio
Synthesis of a novel tetra-phenol π-extended phenazine and its application as an organo-photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 602-605
7132613 CIFC56 H95 Mo6 N7 O18P 1 21/c 112.4406; 29.2646; 18.9032
90; 92.548; 90
6875.27Jones, Claire F.; Hood, Bethany R.; de Coene, Yovan; Lopez-Poves, Ivan; Champagne, Benoît; Clays, Koen; Fielden, John
Bridge improvement work: maximising non-linear optical performance in polyoxometalate derivatives.
Chemical communications (Cambridge, England), 2024, 60, 1731-1734
7132614 CIFC30 H33 O3 PP 1 21 110.97433; 9.78846; 11.7517
90; 102.023; 90
1234.7Huang, Yu; Zhang, Yulong; Pan, Li; Wu, Qian; Li, Ning; Shi, Enxue; Xiao, Junhua
CAMDOL-enabled diastereoselective synthesis of α-substituted phosphonates.
Chemical communications (Cambridge, England), 2024, 60, 1924-1927
7132615 CIFC27 H34 N3 O3 PP 1 21 111.2201; 8.4447; 13.8792
90; 98.303; 90
1301.28Chen, Zi-Jia; Fan, Ling-Jie; Xie, Pei-Pei; Qian, Pu-Fan; Hu, Xinquan; Zhou, Tao; Shi, Bing-Feng
Pd(II)-Catalyzed enantioselective C-H olefination toward the synthesis of <i>P</i>-stereogenic phosphinamides.
Chemical communications (Cambridge, England), 2024, 60, 1623-1626
7132616 CIFC44 H54 B N3 Ni PP 1 21/c 114.5193; 29.0183; 9.5279
90; 103.894; 90
3896.89Bermejo, José; Ortega-Lepe, Isabel; Santos, Laura L.; Rendón, Nuria; López-Serrano, Joaquín; Álvarez, Eleuterio; Suárez, Andrés
Nitrous oxide activation by picoline-derived Ni-CNP hydrides.
Chemical communications (Cambridge, England), 2024, 60, 1575-1578
7132617 CIFC26 H36 N3 Ni O PP 42/n :221.355; 21.355; 11.6688
90; 90; 90
5321.4Bermejo, José; Ortega-Lepe, Isabel; Santos, Laura L.; Rendón, Nuria; López-Serrano, Joaquín; Álvarez, Eleuterio; Suárez, Andrés
Nitrous oxide activation by picoline-derived Ni-CNP hydrides.
Chemical communications (Cambridge, England), 2024, 60, 1575-1578
7132618 CIFC10 H32 Bi I9 N4C m c m11.8846; 11.8525; 23.941
90; 90; 90
3372.4Wang, Yu-Yin; Kang, Huai-Yuan; Zhang, Shao-Ya; Qu, Hao; Zhu, Lin; Zhao, Dan; Li, Xian-Feng; Lei, Xiao-Wu; Yue, Cheng-Yang
Exploring 0D lead-free metal halide with highly efficient blue light emission and high-sensitivity photodetection.
Chemical communications (Cambridge, England), 2024, 60, 2784-2787
7132619 CIFC52 H98 N4 O6 Si6P -111.9643; 16.5858; 17.5688
90.529; 98.876; 109.35
3243.16Kim, Junghwan; Kim, Chungryeol; Lee, Dongwhan
Fluoride-triggered phase transition of metallogels for on-demand <i>in situ</i> containment of fluids.
Chemical communications (Cambridge, England), 2024, 60, 1762-1765
7132620 CIFC70 H134 N4 O6 Si6P -115.9929; 16.1504; 17.3188
79.449; 65.041; 78.584
3950.26Kim, Junghwan; Kim, Chungryeol; Lee, Dongwhan
Fluoride-triggered phase transition of metallogels for on-demand <i>in situ</i> containment of fluids.
Chemical communications (Cambridge, England), 2024, 60, 1762-1765
7132621 CIFC36 H26 N8 Ni O4P b c n12.655; 15.538; 17.066
90; 90; 90
3355.7Nogita, Kohei; Sugahara, Takaya; Miki, Koji; Mu, Huiying; Kobayashi, Minoru; Harada, Hiroshi; Ohe, Kouichi
A reductively convertible nickel phthalocyanine precursor as a biological thiol-responsive turn-on photoacoustic contrast agent.
Chemical communications (Cambridge, England), 2024, 60, 1472-1475
7132622 CIFC18 H17 Cl N2 O2P c c n21.1441; 11.5844; 12.8398
90; 90; 90
3145Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132623 CIFC18 H18 N2 O3 SP 1 21/c 113.7896; 9.0412; 13.8981
90; 108.87; 90
1639.61Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132624 CIFC19 H18 N2 O2P 1 21/n 19.1979; 15.6759; 10.7636
90; 95.704; 90
1544.27Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132625 CIFC20 H17 Cl N2 O2P n a 2110.2787; 11.9147; 27.5592
90; 90; 90
3375.1Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132626 CIFC13 H9 N O3P 21 21 213.8378; 8.6367; 29.4303
90; 90; 90
975.49Chand, Tapasi; Gupta, Princi; Oza, Nehali; Kapur, Manmohan
Cobalt(II)-catalyzed <i>peri</i>-C(sp<sup>2</sup>)-H selective hydroxylation of naphthalene monoimides.
Chemical communications (Cambridge, England), 2024, 60, 1770-1773
7132627 CIFC38.49 H30.98 Cl3.98 P2 SbF d d 228.25; 31.29; 15.7735
90; 90; 90
13943Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132628 CIFC38.5 H31 Br Cl3 P2 SbF d d 227.674; 31.304; 16.183
90; 90; 90
14019Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132629 CIFC39 H32 Cl4 F6 P2 Sb2P 1 21/n 114.6987; 15.5168; 17.522
90; 93.975; 90
3986.7Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132630 CIFC40 H34 Au Bi Cl8 P2P 1 21/c 111.6409; 23.1633; 15.8194
90; 97.161; 90
4232.3Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132631 CIFC141 H87.9 B2 Br2 Cl5.9 F48.05 P4 Sb2P -112.135; 16.6073; 18.5495
107.079; 95.331; 99.299
3487.2Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132632 CIFC41 H37 Br F6 O P2 Sb2P 1 21/c 110.3202; 20.6841; 18.508
90; 92.122; 90
3948.1Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132633 CIFC40 H34 Au Cl8 P2 SbP 1 21/c 111.6084; 23.1906; 15.8524
90; 97.164; 90
4234.2Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132634 CIFC27 H21 In N6P 1 21/c 116.1797; 15.4641; 9.7077
90; 99.032; 90
2398.8Fu, Li-Zhi; He, Piao; Wang, Jia-Wei; Ma, Fan; Liu, Chao; Chen, Guo; Yi, Xiao-Yi
Mononuclear indium(III) photosensitizers for photo-dehalogenation and olefin reduction.
Chemical communications (Cambridge, England), 2024, 60, 1595-1598
7132635 CIFC33 H33 In N6P -19.9431; 10.4086; 14.78
83.547; 80.299; 74.885
1451.83Fu, Li-Zhi; He, Piao; Wang, Jia-Wei; Ma, Fan; Liu, Chao; Chen, Guo; Yi, Xiao-Yi
Mononuclear indium(III) photosensitizers for photo-dehalogenation and olefin reduction.
Chemical communications (Cambridge, England), 2024, 60, 1595-1598
7132636 CIFC54 H72 B2 N4 SiP 1 21/c 112.4737; 14.971; 26.1547
90; 92.786; 90
4878.5Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132637 CIFC52 H68 B2 N4 SiP 1 21/c 122.4231; 11.6708; 19.4398
90; 113.005; 90
4682.72Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132638 CIFC110 H142 B4 N8 Si2P -111.641; 12.3141; 17.9847
95.791; 101.108; 104.877
2414.05Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132639 CIFC54 H72 B2 N4 SiI 1 2/a 124.18452; 11.44862; 68.9173
90; 90.4985; 90
19081.1Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132640 CIFC18 H37 BrP -15.561; 7.204; 46.69
87.22; 87.14; 89.974
1865.9Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132641 CIFC35 H69 Br2 N S2P -18.7215; 9.0562; 25.5173
93.301; 91.998; 106.02
1931.3Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132642 CIFC21 H40 Br N S2P -18.6976; 9.0477; 15.3351
96.503; 101.075; 100.606
1150.16Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132643 CIFC35 H73 N O4 S3P 1 21 15.0644; 7.3853; 51.831
90; 90.179; 90
1938.58Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132644 CIFC17 H16 N2P 1 21/c 112.0756; 8.8912; 12.87
90; 92.604; 90
1380.4Zhao, Mi-Na; Yang, Zi-Mo; Li, Lian-Qing
DMF as an amine source: iron-catalyzed cyclization of 2<i>H</i>-azirines to imidazoles.
Chemical communications (Cambridge, England), 2024, 60, 1904-1907
7132645 CIFC39 H27 N3 SP -110.2867; 12.154; 12.446
79.931; 88.875; 74.591
1476.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132646 CIFC39 H27 N3 OP 1 21/c 114.239; 8.5693; 23.345
90; 102.743; 90
2778.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132647 CIFC40 H29 Cl2 N3 O SP -110.8035; 11.2186; 15.653
69.437; 83.85; 70.803
1677.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132648 CIFC39 H27 N3 O SP 1 21/c 117.993; 17.184; 9.741
90; 103.718; 90
2925.9Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132649 CIFC39 H27 N3 SP -110.141; 10.944; 15.802
90.812; 103.552; 114.74
1535.9Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132650 CIFC32 H41 F6 N PP -111.0504; 11.3069; 13.576
112.089; 90.039; 102.919
1525.21Inoue, Takeru; Matsuura, Yuuka; Horii, Koki; Konishi, Akihito; Nishida, Jun-Ichi; Yasuda, Makoto; Kawase, Takeshi
<i>N</i>-2,6-Di(isopropyl)phenyl-2-azaphenalenyl radical cations.
Chemical communications (Cambridge, England), 2024, 60, 1735-1738
7132651 CIFC17 H14 N3 O2P -17.1044; 10.0383; 10.7169
102.103; 109.324; 102.128
672.07Kuroda, Yusuke; Krell, Maya; Kurokawa, Kazuma; Takasu, Kiyosei
Synthesis of mesoionic triazolones <i>via</i> a formal [3+2] cycloaddition between 4-phenyl-1,2,4-triazoline-3,5-dione and alkynes.
Chemical communications (Cambridge, England), 2024, 60, 1719-1722
7132652 CIFC46 H38 N2 O3 PtP -110.8643; 11.6179; 14.5758
77.263; 82.321; 84.958
1775.15Ikeshita, Masahiro; Watanabe, Shinya; Suzuki, Seika; Tanaka, Shota; Hattori, Shingo; Shinozaki, Kazuteru; Imai, Yoshitane; Tsuno, Takashi
Circularly polarized phosphorescence with a large dissymmetry factor from a helical platinum(II) complex.
Chemical communications (Cambridge, England), 2024, 60, 2413-2416
7132653 CIFC30 H24 N2 O PtP 1 21/n 111.8288; 15.4199; 12.409
90; 98.051; 90
2241.08Ikeshita, Masahiro; Watanabe, Shinya; Suzuki, Seika; Tanaka, Shota; Hattori, Shingo; Shinozaki, Kazuteru; Imai, Yoshitane; Tsuno, Takashi
Circularly polarized phosphorescence with a large dissymmetry factor from a helical platinum(II) complex.
Chemical communications (Cambridge, England), 2024, 60, 2413-2416
7132654 CIFC20 H40 N6 ZnC 1 2/c 115.4081; 10.2686; 15.6427
90; 99.301; 90
2442.44Zhang, Xiaofeng; Li, Yinghua; Fan, Weibin; Huang, Deguang
Direct transformation of nitriles to cyanide using chloride anion as catalyst.
Chemical communications (Cambridge, England), 2024, 60, 2058-2061
7132655 CIFC57 H34 Cl Co N6 O5P -110.5787; 13.3611; 18.6693
73.222; 89.394; 84.62
2514.9Bulbul, Amir Sohel; Rathour, Vikram; Ganesan, Vellaichamy; Sankar, Muniappan
π-Extended nonplanar cobalt porphyrins immobilized on MWCNTs as efficient electrocatalysts for selective oxygen reduction reaction.
Chemical communications (Cambridge, England), 2024, 60, 3146-3149
7132656 CIFC36 H48 Cl2 Cu2 N10 O12P -111.652; 13.232; 16.02
106.82; 96.99; 110.12
2151.7De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132657 CIFC12 H20 Cu F6 N4 O8 S2P 1 21/c 110.686; 14.011; 8.0619
90; 110.87; 90
1127.8De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132658 CIFC40 H52 Cu2 F6 N10 O10 S2P n m a13.529; 20.929; 16.907
90; 90; 90
4787.2De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132659 CIFC37.12 H54.51 B2 Cl0.37 Cu2 F8 N10.38 O6.26P -111.5059; 15.193; 15.47
76.645; 73.531; 68.4
2386.8De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132660 CIFC15 H20 N4 O7P 1 21/c 111.301; 23.093; 6.9978
90; 105.89; 90
1756.5De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132661 CIFC126 H102 N6 S6I a -333.06; 33.06; 33.06
90; 90; 90
36133.4Yamamoto, Koji; Tsutsui, Kanta; Tanuma, Miho; Ito, Kaname; Wakamatsu, Kan; Yamamoto, Koji; Nakamura, Yosuke
Phenothiazine cyclic hexamers: synthesis, properties, and complexation behavior with C<sub>60</sub>.
Chemical communications (Cambridge, England), 2024, 60, 2220-2223
7132662 CIFC84 H98 N13 O24 Sc3P 1 21/n 115.847; 16.418; 34.089
90; 101.579; 90
8689Wang, Hao; Shi, Le; Xiong, Zhangyi; Ma, Si; Cao, Honghao; Cai, Shijia; Qiao, Zhiwei; Pan, Jun; Chen, Zhijie
A two-dimensional metal-organic framework assembled from scandium-based cages for the selective capture of sulfur hexafluoride.
Chemical communications (Cambridge, England), 2024, 60, 2397-2400
7132663 CIFC25 H16 F3 N3 O2P 1 21/c 111.571; 21.464; 8.872
90; 107.385; 90
2102.8Lai, Dipti; Bhattacharjee, Suvam; Mandal, Saurodeep; Ghosh, Sumit; Sahoo, Prithidipa; Sinha, Subrata; Hajra, Alakananda
Iodine(III)-promoted oxidative carbotrifluoromethylation of maleimides with imidazopyridines and Langlois' reagent.
Chemical communications (Cambridge, England), 2024, 60, 2232-2235
7132664 CIFC38 H20 Co N6I 41/a :213.6416; 13.6416; 14.5402
90; 90; 90
2705.83Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132665 CIFC38 H20 Fe N6I 41/a :213.7275; 13.7275; 14.5027
90; 90; 90
2732.95Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132666 CIFC36 H20 Cl2 Mn N4I 41/a :213.789; 13.789; 14.4334
90; 90; 90
2744.32Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132667 CIFC360 H380 B2 Cu58 F8 O12 P4 S36I 41/a c d :250.9312; 50.9312; 64.4799
90; 90; 90
167260Zhang, Qian; Zheng, Hao; Zhou, Jie; Yang, Jia-Ji; Xu, Kai-Yue; Shen, Lian-Yun; Guan, Zong-Jie; Yang, Yang
A bowl-shaped phosphangulene-protected cubic Cu<sub>58</sub> nanocluster.
Chemical communications (Cambridge, England), 2024, 60, 2389-2392
7132668 CIFC32 H34 Cl2 N2 O4P 21 21 2110.2222; 10.4342; 27.3088
90; 90; 90
2912.77Qiu, Xujun; Seibert, Jasmin; Fuhr, Olaf; Biedermann, Frank; Bräse, Stefan
Reversing the stereoselectivity of intramolecular [2+2] photocycloaddition utilizing cucurbit[8]uril as a molecular flask.
Chemical communications (Cambridge, England), 2024, 60, 3267-3270
7132669 CIFC38 H46 N10 O8 P4P -19.9127; 12.0311; 17.7893
96.019; 99.704; 95.561
2065.42Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132670 CIFC15 H18.8 N5 O2 PP -19.0435; 10.15596; 10.73364
108.653; 99.9637; 113.648
802.4Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132671 CIFC52 H80 N20 O12 P4 Zn2P 1 21/n 117.7137; 10.1405; 18.5083
90; 92.467; 90
3321.49Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132672 CIFC46 H66 Co2 N18 O10 P4P 1 21/n 112.2983; 10.2366; 22.8341
90; 94.766; 90
2864.7Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132673 CIFC52 H80 Co2 N20 O12 P4P 1 21/n 117.5968; 10.1687; 18.3843
90; 92.14; 90
3287.3Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132674 CIFB2 F O4 SbP -14.3436; 6.3169; 7.0009
92.888; 95.126; 104.803
184.44Hu, Chenhui; Wu, Mengfan; Han, Jian; Yang, Zhihua; Han, Shujuan; Pan, Shilie
New antimony fluorooxoborates with strong birefringence and unprecedented structural characterisation.
Chemical communications (Cambridge, England), 2024, 60, 2653-2656
7132675 CIFC19 H16 F2 O2P c a 217.534; 12.716; 15.945
90; 90; 90
1527.6Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132676 CIFC27 H24 N4 OI 41/a :224.3936; 24.3936; 16.9622
90; 90; 90
10093.3Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132677 CIFC27 H24 N4 OP b c n26.264; 9.4519; 18.6059
90; 90; 90
4618.8Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132678 CIFC27 H22 Cl2 N4 OP 1 21 110.1692; 9.7507; 23.6934
90; 101.686; 90
2300.67Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132679 CIFC23 H18 Br N3 O2P 1 21/c 17.8608; 18.2829; 13.4885
90; 96.3335; 90
1926.7Aghaie, Kimia; Amiri, Kamran; Rezaei-Gohar, Mohammad; Rominger, Frank; Dar'in, Dmitry; Sapegin, Alexander; Balalaie, Saeed
Transition-metal-free intramolecular double hydrofunctionalization of alkyne to access 6/7/5-fused heterocyclic skeletons.
Chemical communications (Cambridge, England), 2024, 60, 2661-2664
7132680 CIFC23 H18 Br N3 OP 1 21/n 19.9612; 15.0034; 13.3232
90; 99.6334; 90
1963.1Aghaie, Kimia; Amiri, Kamran; Rezaei-Gohar, Mohammad; Rominger, Frank; Dar'in, Dmitry; Sapegin, Alexander; Balalaie, Saeed
Transition-metal-free intramolecular double hydrofunctionalization of alkyne to access 6/7/5-fused heterocyclic skeletons.
Chemical communications (Cambridge, England), 2024, 60, 2661-2664
7132681 CIFC26 H19 Mo O6 PP 1 21/c 19.4364; 30.672; 24.941
90; 94.189; 90
7199.5Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132682 CIFC24 H24 Br O3 PP -19.5566; 10.874; 12.1513
97.716; 112.057; 109.43
1054.03Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132683 CIFC21 H19 O PP -18.1143; 8.9827; 12.4136
94.652; 90.566; 113.742
824.6Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132684 CIFC24 H24 Br O2 PP -18.8789; 9.5863; 13.4826
84.831; 87.383; 65.062
1036.32Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132685 CIFC28 H23 Mo O6 PP -19.4957; 18.3164; 22.5419
99.296; 92.701; 95.011
3846.9Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132686 CIFC29 H26 Br O2 PP -18.9276; 10.5777; 14.307
69.469; 84.259; 72.909
1209.4Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132687 CIFC20 H15 F OP b c a16.4099; 10.0684; 18.6788
90; 90; 90
3086.1Zhang, Zhou; Li, Jin; Cai, Zhiwei; Kang, Songyao; Wang, Jian; Cui, Yue; Han, Siyuan; Sheng, Lei; Yin, Qing; Dai, Ang; Zhao, Weining; Zhao, Fangyuan
Electrochemical aerobic Wacker-type oxygenation of triaryl substituted alkenes to 1,2,2-triarylethanones.
Chemical communications (Cambridge, England), 2024, 60, 3035-3038
7132688 CIFC23 H18 N2 OP 21 21 216.2987; 7.8754; 36.641
90; 90; 90
1817.57Wang, Mingxu; Gao, Ying; Zhao, Xiao-Jing; Gao, Lu; He, Yonghui
Electrochemical multicomponent [2+2+1] cascade cyclization of enaminones and primary amines towards the synthesis of 4-acylimidazoles.
Chemical communications (Cambridge, England), 2024, 60, 2677-2680
7132689 CIFC56 H71 Cl Ga Ge N2P -111.3222; 12.2948; 20.0701
98.212; 91.794; 114.236
2508.9Bücker, Anna; Gehlhaar, Alexander; Wölper, Christoph; Schulz, Stephan
Activation of non-polar bonds by an electron-rich gallagermylene.
Chemical communications (Cambridge, England), 2024, 60, 2902-2905
7132690 CIFC53 H66 Cl Ga Ge N2 P4C 1 2/c 145.016; 10.0401; 23.339
90; 102.56; 90
10296Bücker, Anna; Gehlhaar, Alexander; Wölper, Christoph; Schulz, Stephan
Activation of non-polar bonds by an electron-rich gallagermylene.
Chemical communications (Cambridge, England), 2024, 60, 2902-2905
7132691 CIFC33 H21 F OP 21 21 218.733; 16.125; 16.631
90; 90; 90
2342Hore, Soumyadip; Singh, Abhijeet; Singh, Ravi P.
Asymmetric 1,2-diaxial synthesis of bi-(hetero)aryl benzofulvene atropisomers <i>via</i> transient directing group-assisted dehydrogenative coupling.
Chemical communications (Cambridge, England), 2024, 60, 2524-2527
7132692 CIFC44 H36 Br Cl2 N3P 1 21/c 115.5477; 14.2729; 16.1793
90; 92.941; 90
3585.6Bernt, Felix; Leonhardt, Christopher M.; Schatz, Dominic; Wegner, Hermann A.
Synthesis and investigation of a <i>meta</i>[6]cycloparaphenylene gold(I) <i>N</i>-heterocyclic carbene complex.
Chemical communications (Cambridge, England), 2024, 60, 3055-3058
7132693 CIFC57 H46 Au Br Cl8 N2P 1 21/m 110.2999; 14.4369; 17.7726
90; 98.815; 90
2611.5Bernt, Felix; Leonhardt, Christopher M.; Schatz, Dominic; Wegner, Hermann A.
Synthesis and investigation of a <i>meta</i>[6]cycloparaphenylene gold(I) <i>N</i>-heterocyclic carbene complex.
Chemical communications (Cambridge, England), 2024, 60, 3055-3058
7132694 CIFC39 H51 O P SiP -114.1352; 15.4491; 19.4502
85.75; 69.641; 64.337
3574.6Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132695 CIFC46 H32 Cl6 O2 P2 SP -114.0465; 14.1358; 14.4268
118.189; 92.506; 114.771
2185.5Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132696 CIFC29 H21 O2 PP 1 21/c 19.475; 18.8265; 12.489
90; 109.249; 90
2103.26Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132697 CIFC29 H22 N3 O PP -19.9714; 10.8463; 22.5248
77.043; 86.915; 82.273
2351.83Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132698 CIFC24 H26 O5 SP 1 21/n 110.416; 19.09; 11.659
90; 113.372; 90
2128.1Mishra, Manmath; Verma, Kshitiz; Banerjee, Sonbidya; Punniyamurthy, Tharmalingam
Iron-catalyzed cascade C-C/C-O bond formation of 2,4-dienals with donor-acceptor cyclopropanes: access to functionalized hexahydrocyclopentapyrans.
Chemical communications (Cambridge, England), 2024, 60, 2788-2791
7132699 CIFC14 H19 N O3P 1 21/c 18.4622; 17.4106; 10.0167
90; 109.344; 90
1392.47Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132700 CIFC17 H17 N O3P 1 21/n 110.8048; 10.1624; 14.3028
90; 110.088; 90
1474.95Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132701 CIFC13 H16 Cl N O3P 1 21/c 18.5014; 16.7568; 10.0698
90; 105.68; 90
1381.12Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132702 CIFC16 H14 Cl N O3P 1 21/c 110.9337; 9.852; 14.5888
90; 111.998; 90
1457.08Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132703 CIFC27 H35 Cl N2 O6P 1 21 18.5052; 16.9899; 10.0551
90; 107.507; 90
1385.69Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132704 CIFC30 H33 Cl N2 O6P 1 21 110.7599; 9.7943; 14.5273
90; 111.649; 90
1422.98Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132705 CIFC29 H30 Cl2 N2 O6P 1 21 110.7438; 9.7103; 14.4644
90; 110.923; 90
1409.5Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132706 CIFC16 H15 N O3P 1 21/c 111.2259; 9.0079; 14.0101
90; 107.097; 90
1354.12Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132707 CIFC31 H36 N2 O6P 1 21 110.6827; 9.9438; 14.441
90; 110.66; 90
1435.37Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132708 CIFC33 H31 Cl N2 O6P 1 21 110.8824; 10.0217; 14.4325
90; 111.003; 90
1469.44Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132709 CIFC13 H17 N O3P 1 21/c 110.7023; 9.0828; 13.337
90; 103.692; 90
1259.61Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132710 CIFC30 H33 Cl N2 O6P 1 21 110.7094; 9.8205; 14.5002
90; 111.286; 90
1420.97Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132711 CIFC31 H30 F6 N2 O6P 1 21 113.8243; 9.1832; 13.8585
90; 117.871; 90
1555.27Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132712 CIFC33 H29 F3 N2 O6P 1 21 112.9498; 9.6063; 13.1925
90; 117.118; 90
1460.7Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132713 CIFC29 H32 N2 O6P 1 21 110.9173; 9.1344; 14.1599
90; 108.014; 90
1342.85Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132714 CIFC30 H31 F3 N2 O6P 1 21 111.4316; 9.5763; 14.2272
90; 111.456; 90
1449.55Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132715 CIFC14 H16 F3 N O3P 1 21/c 18.966; 17.0296; 10.0714
90; 107.371; 90
1467.64Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132716 CIFC20 H38 K16 N2 Na10.5 O218 P7 W39 Zr3P 31 2 122.6518; 22.6518; 75.9558
90; 90; 120
33751.8Yang, Dongsheng; Liu, Lihua; Zhang, Yunfan; Zhang, Miao; Ma, Pengtao; Wang, Jingping; Niu, Jingyang
A wheel-shaped Zr-substituted phosphotungstate [{Zr(C<sub>2</sub>O<sub>4</sub>)<sub>2</sub>}<sub>3</sub> (PO<sub>4</sub>)(P<sub>6</sub>W<sub>39</sub>O<sub>150</sub>)]<sup>39-</sup> with tunable proton conduction properties.
Chemical communications (Cambridge, England), 2024, 60, 3043-3046
7132717 CIFC20 H48 N10 P2 UP 1 21/n 19.909; 10.674; 14.833
90; 104.484; 90
1519Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132718 CIFC40 H98 N10 P4 U2P -110.769; 13.579; 20.817
82.853; 79.684; 69.571
2800.2Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132719 CIFC40 H96 N20 P4 U2P 21 21 210.5753; 27.797; 10.3786
90; 90; 90
3050.9Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132720 CIFC40 H96 N20 P4 U2C 1 2/c 125.24; 10.392; 25.465
90; 110.915; 90
6239Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132721 CIFC40 H96 N20 P4 U2C 1 2/c 125.206; 10.392; 25.457
90; 110.647; 90
6240Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132722 CIFC20 H48 N10 P2 UC 1 2/c 125.309; 10.4218; 25.538
90; 110.799; 90
6297.1Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132723 CIFC40 H96 N20 P4 U2C 1 2/c 125.279; 10.4213; 25.477
90; 110.786; 90
6274.8Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132724 CIFC40 H96 N20 P4 U2P 21 21 210.5761; 27.7942; 10.3688
90; 90; 90
3048Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132725 CIFC80 H192 N40 P8 U4P 1 2/n 124.9458; 10.2858; 25.3172
90; 111.158; 90
6058.2Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132726 CIFC20 H48 N10 P2 UP 1 21/n 110.1931; 10.6719; 14.9477
90; 102.736; 90
1586Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132727 CIFC20 H48 N10 P2 UP 1 21/n 19.8845; 10.6539; 14.7678
90; 104.838; 90
1503.32Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132728 CIFC40 H96 N20 P4 U2P 21 21 210.5757; 27.8005; 10.3708
90; 90; 90
3049.1Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132729 CIFC20 H48 N10 P2 UP 1 2/n 124.9421; 10.2665; 25.3542
90; 111.169; 90
6054.3Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132730 CIFC16 H14 Cl2 N2 O2 SnC 1 c 110.7059; 14.2716; 10.8582
90; 101.977; 90
1622.91Žáková, Andrea; Saha, Pritha; Paparakis, Alexandros; Zábranský, Martin; Gastelu, Gabriela; Kukla, Jaroslav; Uranga, Jorge G.; Hulla, Martin
Hexacoordinated tin complexes catalyse imine hydrogenation with H<sub>2</sub>.
Chemical communications (Cambridge, England), 2024, 60, 3287-3290
7132731 CIFC51 H40 B Cl4 N OP -19.2148; 13.8751; 16.7722
74.99; 87.948; 80.579
2043.28Huang, Yong; Jia, Mengjiao; Li, Chuan; Yang, Yang; He, Yuling; Luo, Yanju; Huang, Yan; Zhou, Liang; Lu, Zhiyun
A spiroacridine-based thermally activated delayed fluorescence emitter for high-efficiency and narrow-band deep-blue OLEDs.
Chemical communications (Cambridge, England), 2024, 60, 3194-3197
7132732 CIFC194 H142 Ag14 Cl4 F36 P8 Pd S6P 1 21/c 117.46; 36.131; 18.471
90; 110.07; 90
10945Ma, Along; Ren, Yonggang; Zuo, Yang; Wang, Jiawei; Huang, Shutong; Ma, Xiaoshuang; Wang, Shuxin
Ligand-controlled exposure of active sites on the Pd<sub>1</sub>Ag<sub>14</sub> nanocluster surface to boost electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 3162-3165
7132733 CIFC183 H171 Ag14 O21 P7 Pd S6P -119.457; 20.805; 27.84
82.006; 74.854; 84.149
10747Ma, Along; Ren, Yonggang; Zuo, Yang; Wang, Jiawei; Huang, Shutong; Ma, Xiaoshuang; Wang, Shuxin
Ligand-controlled exposure of active sites on the Pd<sub>1</sub>Ag<sub>14</sub> nanocluster surface to boost electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 3162-3165
7132734 CIFC18 H15 Br O3P 1 21 17.2004; 6.8661; 16.0022
90; 100.88; 90
776.91Sarkar, Rahul; Korell, Alexander; Schneider, Christoph
Organocatalytic enantioselective oxa-Piancatelli rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 3063-3066
7132735 CIFC66 H58 Hg O P4 S2C 1 2/c 124.571; 14.09; 20.038
90; 122.893; 90
5825Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132736 CIFC31 H26 P2 SP 1 21/n 19.72967; 15.22975; 16.93649
90; 91.2641; 90
2509.05Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132737 CIFC58 H63 Cl P2 S UP -112.0774; 14.1627; 14.3748
94.016; 90.702; 93.297
2448.4Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132738 CIFC43 H49 K O6 P2 SP -19.4692; 10.8945; 21.4146
77.036; 83.374; 73.667
2062.75Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132739 CIFC58 H63 Cl P2 S ThP -112.1389; 14.1799; 14.3984
94.193; 90.436; 93.016
2468.15Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132740 CIFC19 H20 N2 OP 1 21/c 18.637; 13.293; 29.631
90; 96.679; 90
3378.9Zhang, Min; Zheng, Yongpeng; Jin, Yangbin; Jiang, Huanfeng; Wu, Wanqing
Palladium-catalyzed ligand-regulated divergent synthesis of pyrrole[2,3-<i>b</i>]indoles and ureas from 2-ethynylanilines and isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2950-2953
7132741 CIFC26 H28 N4C 1 2/c 115.2301; 10.2357; 28.4109
90; 95.828; 90
4406.1Zhang, Min; Zheng, Yongpeng; Jin, Yangbin; Jiang, Huanfeng; Wu, Wanqing
Palladium-catalyzed ligand-regulated divergent synthesis of pyrrole[2,3-<i>b</i>]indoles and ureas from 2-ethynylanilines and isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2950-2953
7132742 CIFC17 H14 B F3 N2P -18.4898; 11.7179; 16.2792
90.732; 99.945; 95.106
1588.18McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132743 CIFC17 H15 B F4 N2P 1 21 110.3062; 7.7018; 10.3247
90; 101.056; 90
804.326McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132744 CIFC17 H14 B F3 N2P -18.359; 11.6452; 16.1214
90.762; 100.271; 94.709
1538.31McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132745 CIFC5 H8 Er N3 O8P c c a8.2526; 6.5427; 19.313
90; 90; 90
1042.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132746 CIFC5 H8 Er N3 O8P c c a8.1956; 6.534; 19.322
90; 90; 90
1034.7Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132747 CIFC5 H8 Er N3 O8P c c a8.4551; 6.584; 19.2134
90; 90; 90
1069.58Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132748 CIFC5 H8 Er N3 O8P c c a7.8462; 6.5142; 19.58
90; 90; 90
1000.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132749 CIFC5 H8 Er N3 O8P c c a8.3154; 6.549; 19.234
90; 90; 90
1047.44Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132750 CIFC5 H8 Er N3 O8P c c a8.3583; 6.5585; 19.218
90; 90; 90
1053.49Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132751 CIFC5 H8 Er N3 O8P c c a7.801; 6.5107; 19.64
90; 90; 90
997.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132752 CIFC5 H8 Er N3 O8P c c a8.4958; 6.5946; 19.201
90; 90; 90
1075.76Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132753 CIFC5 H8 Er N3 O8P c c a7.736; 6.479; 19.71
90; 90; 90
988Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132754 CIFC5 H8 Er N3 O8P c c a8.4154; 6.5724; 19.21
90; 90; 90
1062.49Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132755 CIFC6 H10 Er N O8P 1 2/n 19.1183; 8.948; 13.1042
90; 96.446; 90
1062.4Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132756 CIFC6 H10 Er N O8P 1 2/n 19.1326; 8.974; 13.1405
90; 96.41; 90
1070.2Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132757 CIFC6 H10 Er N O8P 1 2/n 19.1263; 8.963; 13.1305
90; 96.44; 90
1067.3Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132758 CIFC6 H10 Er N O8P 1 2/a 19.0759; 8.863; 6.4822
90; 96.228; 90
518.3Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132759 CIFC6 H10 Er N O8P 1 2/a 19.0907; 8.903; 6.5091
90; 96.38; 90
523.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132760 CIFC6 H10 Er N O8P 1 2/n 19.1539; 8.9987; 13.1797
90; 96.604; 90
1078.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132761 CIFC6 H10 Er N O8P 1 2/a 19.0471; 8.792; 6.4339
90; 96.131; 90
508.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132762 CIFC6 H10 Er N O8P 1 2/n 19.1533; 8.9945; 13.1812
90; 96.747; 90
1077.68Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132763 CIFC6 H10 Er N O8P 1 2/a 19.1025; 8.913; 6.5273
90; 96.442; 90
526.2Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132764 CIFC141 H123 Ag4 Cd6 N7 O2 S16I 1 2/m 115.6408; 26.8262; 40.7797
90; 90.156; 90
17110.4Li, Yan-Ling; Liu, Yu-Dong; Li, Wei-Li; Li, Fu-An; Feng, Yun-Xiao; Luo, Xiao-Qiang; Han, Yong-Jun
Ligand engineering to achieve synergistic properties in a 2D bilayer supertetrahedral chalcogenide cluster-based assembled material.
Chemical communications (Cambridge, England), 2024, 60, 3279-3282
7132765 CIFC35 H36 N2 O9P -110.6256; 14.683; 20.9217
110.478; 90.035; 90.542
3057.7Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132766 CIFC71 H73 Cl3 N4 O16 S2P -110.084; 15.1221; 22.373
100.593; 94.039; 95.97
3321.3Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132767 CIFC124 H120 N8 O24P 1 21/n 117.0682; 11.8271; 27.346
90; 106.721; 90
5286.9Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132768 CIFC23 H18 Cl3 N O2P 21 21 215.5787; 13.2751; 27.4431
90; 90; 90
2032.4Wei, Jian; Du, Zhongjian; Wang, Xu; Ji, Chenlei; Li, Longji; You, Yang'en
Palladium-catalyzed enantioselective arylation of trichloro- or tri-/difluoroacetaldimine precursors.
Chemical communications (Cambridge, England), 2024, 60, 3303-3306
7132769 CIFC29 H31 N3 O6 SP -18.2702; 12.562; 13.769
89.503; 79.822; 87.707
1406.8Samantaray, Swati; Maharana, Prabhat Kumar; Kar, Subhradeep; Saha, Sharajit; Punniyamurthy, Tharmalingam
Redox-neutral zinc-catalyzed cascade [1,4]-H shift/annulation of diaziridines with donor-acceptor aziridines.
Chemical communications (Cambridge, England), 2024, 60, 3441-3444
7132770 CIFC13 H14 Cl N O4 SP 1 21 15.5934; 10.4137; 12.5612
90; 97.969; 90
724.6Wan, Chuan; Yang, Dongyan; Guo, Xiaochun; Zhang, Tuanjie; Ruan, Zhijun; Dai, Chuan; Xing, Yun; Yin, Feng; Wang, Rui; Li, Zigang
β-Carbonyl sulfonium enables cysteine-specific bioconjugation for activity-based protein profiling in live cells.
Chemical communications (Cambridge, England), 2024, 60, 3725-3728
7132771 CIFC26.68 H32.49 N6 O1.56R -3 :H37.3204; 37.3204; 9.7227
90; 90; 120
11727.6Kang, Xiang; Zhang, Mingtao; Tang, Weiwei; Gong, Junbo
Growth "self-inhibition" of irbesartan desmotrope: surface intra-annular tautomer inter-conversion is the culprit.
Chemical communications (Cambridge, England), 2024, 60, 3511-3514
7132772 CIFC12 H14 Cl4 N2 O4 Pb S2P 1 21/c 14.3263; 18.5138; 12.3948
90; 97.504; 90
984.27Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132773 CIFC12 H12 Br4 N2 O4 Pb S2P 1 21/c 14.4621; 19.0334; 12.5804
90; 98.489; 90
1056.73Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132774 CIFC12 H12 I4 N2 O4 Pb S2P 1 21/c 14.6903; 19.9065; 12.82
90; 99.393; 90
1180.92Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132775 CIFC62 H66 N10 O14 S4C 1 2/c 137.954; 10.748; 24.5839
90; 93.542; 90
10009.3Huang, Ming-Feng; Cao, Li-Hui; Zhou, Bin
A solvent-controlled photoresponsive ionic hydrogen-bonded organic framework for encryption applications.
Chemical communications (Cambridge, England), 2024, 60, 3437-3440
7132776 CIFC42 H48 N8 O16 S4P 1 21/c 112.9205; 27.6064; 15.3072
90; 113.718; 90
4998.72Huang, Ming-Feng; Cao, Li-Hui; Zhou, Bin
A solvent-controlled photoresponsive ionic hydrogen-bonded organic framework for encryption applications.
Chemical communications (Cambridge, England), 2024, 60, 3437-3440
7132777 CIFC41 H33 N O7 SP 1 21 19.1592; 17.6405; 10.2784
90; 94.192; 90
1656.27Barik, Shilpa; Sankar, Ganga; Biju, Akkattu T.
Enantioselective synthesis of tricyclic oxoquinolines <i>via</i> NHC-catalyzed Michael-aldol-lactamization-dehydration cascade.
Chemical communications (Cambridge, England), 2024, 60, 4290-4293
7132778 CIFC18 H14 Ca F9 N3 O8P 1 21/n 124.1213; 8.1633; 24.2668
90; 98.981; 90
4719.8Baudet, Judith; Lesur, Emilie; Ribéraud, Maxime; Chevalier, Arnaud; D'Anfray, Timothée; Thuéry, Pierre; Audisio, Davide; Taran, Frédéric
Synthesis of sydnonimines from sydnones and their use for bioorthogonal release of isocyanates in cells.
Chemical communications (Cambridge, England), 2024, 60, 3657-3660
7132779 CIFC36 H92 I2 K O10 Si8 UP -113.4213; 15.8641; 16.3965
104.442; 102.934; 96.066
3246.4Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132780 CIFC36 H98 I2 K O11 Si8 UP 1 2/c 114.8717; 15.8095; 28.9025
90; 103.785; 90
6599.7Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132781 CIFC40 H98 I2 K O10 Si8 UC 1 2/c 149.049; 13.108; 21.124
90; 90.054; 90
13581Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132782 CIFC27 H15 B F N5P -18.0536; 8.9238; 15.0934
79.306; 85.035; 65.599
970.63Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132783 CIFC34 H22 B Cl2 N5P -19.3419; 10.0645; 14.7904
91.141; 105.751; 90.019
1338.11Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132784 CIFC16 H13 F2 N OP 1 21/n 110.169; 10.856; 12.0502
90; 102.79; 90
1297.27Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132785 CIFC16 H13 F2 N OP -19.7065; 11.7198; 12.029
77.71; 89.322; 71.433
1265.13Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132786 CIFC210 H228 Ag3 B F4 N36 O24R 3 2 :H38.1751; 38.1751; 37.5163
90; 90; 120
47349Bajpayee, Nikhil; Pophali, Salil; Vijayakanth, Thangavel; Nandi, Shyamapada; Desai, Aamod V.; Kumar, Vinod; Jain, Rahul; Bera, Santu; Shimon, Linda J. W.; Misra, Rajkumar
Metal-driven folding and assembly of a minimal β-sheet into a 3D-porous honeycomb framework.
Chemical communications (Cambridge, England), 2024, 60, 2621-2624
7132787 CIFC76 H65 Cu2 N20 O16.5P 4319.7601; 19.7601; 19.9303
90; 90; 90
7782Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132788 CIFC40 H33 Cl4 Cu2 N9 OP 1 21/n 115.805; 9.323; 27.137
90; 99.835; 90
3939.9Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132789 CIFC41.5 H45.5 N6.5 O18 Tb TiP m -3 n25.9298; 25.9298; 25.9298
90; 90; 90
17434Yao, Qingxia; Pan, Xuze; Si, Xuezhen; Wang, Xin; Zhang, Xiaoying; Hou, Jinle; Su, Jie; Qiu, Yi; Li, Jun
A porous and photoactive Ti-MOF based on a novel tetranuclear [Ti<sub>2</sub>Tb<sub>2</sub>] cluster.
Chemical communications (Cambridge, England), 2024, 60, 2188-2191
7132790 CIFC29 H32 N2 O5P -111.4759; 11.5363; 19.7187
85.779; 79.152; 85.444
2551.2Lai, Jingxiong; Huang, You
A highly diastereoselective (5+1) annulation of allenoates and pyrazolones catalyzed by CH<sub>3</sub>OK.
Chemical communications (Cambridge, England), 2024, 60, 2066-2069
7132791 CIFC10 H19 N O3P 1 21 15.4153; 11.2753; 9.4479
90; 98.633; 90
570.34Zhang, Qiuxin; Zhang, Heng; Geng, Senbai; Zhao, Xian; Liu, Shucheng; Hong, Kun; Pan, Jianming; Yan, Xingchen
Green transformation of CO<sub>2</sub> into γ-amino alcohols with continuous stereocenters.
Chemical communications (Cambridge, England), 2024, 60, 2062-2065
7132792 CIFC52 H52 B2 Hg N14 O4 Se2 W2P -113.7335; 21.8752; 22.673
117.984; 91.487; 103.84
5764.1Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132793 CIFC20 H23 B N6 O2 Se WP 1 21/c 17.9715; 18.2689; 19.7379
90; 101.415; 90
2817.58Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132794 CIFC29 H43 B N6 O2 Si Te WP -110.6281; 11.0432; 15.1354
84.687; 87.521; 75.938
1715.38Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132795 CIFC21 H30 Au B Cl6 N6 O2 S Te WP -111.1523; 11.161; 14.3505
89.093; 89.186; 77.275
1742.02Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132796 CIFC64 H100 B2 Cl4 Cu4 N12 O4 Si2 Te2 W2P 1 21/n 110.9539; 18.7716; 20.4333
90; 102.63; 90
4099.87Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132797 CIFC24 H27 B N8 O2 Te WP 1 21 17.9095; 18.2594; 9.7522
90; 99.742; 90
1388.13Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132798 CIFC23 H31 Au B Cl N6 O2 S Si WP 1 21/m 112.3181; 24.9472; 16.5061
90; 108.592; 90
4807.6Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132799 CIFC26 H27 B N6 O2 Te WP 1 21/n 120.5319; 14.2779; 21.6073
90; 117.804; 90
5602.9Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132800 CIFC33 H28 F3 N3 O2P 21 21 218.2405; 13.6044; 25.8384
90; 90; 90
2896.67Wang, Lan; Lu, Mengxi; Li, Kuan; Yang, Sen; Wang, Lei; Guo, Hongchao
Palladium-catalyzed enantioselective umpolung allylation of amido-tethered allylic carbonates with isatin-derived ketimines.
Chemical communications (Cambridge, England), 2024, 60, 3729-3732
7132801 CIFC22 H17 F N2P 1 21/c 16.2418; 18.1094; 15.2988
90; 96.701; 90
1717.49Qin, Jiaze; Jiang, Shixuan; Luo, Xiaofeng; Wang, Tianqiang; Liu, Peihua; Yuan, Bingxiang; Yan, Rulong
I<sub>2</sub>-catalyzed synthesis of 3-aminopyrrole with homopropargylic amines and nitrosoarenes.
Chemical communications (Cambridge, England), 2024, 60, 3701-3704
7132802 CIFC38 H28 N8P 1 21/n 111.5521; 9.4107; 32.526
90; 95.722; 90
3518.39Zhang, Li; Luo, Yu-Ting; Xiao, Sai-Jin; Fan, Jia-Qi; Tan, Quan-Gen; Sun, Chen; Song, An-Min; Liang, Ru-Ping; Qiu, Jian-Ding
The construction of a stable hydrogen-bonded organic framework for the photocatalytic reduction and removal of uranium.
Chemical communications (Cambridge, England), 2024, 60, 3583-3586
7132803 CIFC19 H17 Br O2P 21 21 217.1586; 11.9651; 18.845
90; 90; 90
1614.1Li, Zheyao; Zhang, Huiwen; Zhao, Lin; Ma, Yueyue; Wu, Qiufang; Ren, Haosong; Lin, Zhongren; Zheng, Jun; Yu, Xinhong
Metal-free β,γ-C(sp<sup>3</sup>)-H difunctionalization of propanols: DMP-initiated asymmetric spirocyclopropanation.
Chemical communications (Cambridge, England), 2024, 60, 3579-3582
7132804 CIFC29 H19 N O5P -19.9434; 11.2111; 11.3362
100.833; 92.317; 115.863
1106.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132805 CIFC29 H18 O6P 1 21/c 18.5559; 26.5; 9.988
90; 99.097; 90
2236.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132806 CIFC27 H23 NP 1 21/n 19.4988; 11.9651; 17.3667
90; 97.139; 90
1958.49Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132807 CIFC16 H14 O2P n a 2116.5657; 5.4295; 14.0697
90; 90; 90
1265.48Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132808 CIFC26 H23.62 Cl0.38 N2 O3 SP 1 21/n 110.908; 15.648; 14.141
90; 112.321; 90
2232.8Wang, Bi; Liang, Ren-Xiao; Shen, Zhen-Lu; Jia, Yi-Xia
Copper-catalyzed intramolecular dearomative aza-Wacker reaction of indole.
Chemical communications (Cambridge, England), 2024, 60, 3858-3861
7132809 CIFC20 H22 O2P 1 21 18.546; 6.518; 15.6
90; 105.428; 90
837.7Magham, Lakshmi Revati; Samad, Abdus; Thopate, Satish B.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
Organocatalytic enantioselective desymmetrization of enal-tethered cyclohexane-1,3-diones.
Chemical communications (Cambridge, England), 2024, 60, 3834-3837
7132810 CIFC18 H20 Cl N O2P -18.3513; 13.4596; 15.583
77.965; 76.1; 77.207
1635.64Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132811 CIFC18 H17 Cl F3 N OP 1 21/c 16.2156; 11.1571; 24.7517
90; 92.551; 90
1714.78Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132812 CIFC17 H24 Cl N OP 1 21/n 19.2235; 7.0079; 25.1221
90; 94.528; 90
1618.76Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132813 CIFC14 H18 Cl N OI 1 2/a 118.5653; 6.3699; 23.6434
90; 108.817; 90
2646.61Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132814 CIFC19 H22 Cl N OP 1 21/n 116.7373; 6.1891; 18.0916
90; 110.509; 90
1755.3Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132815 CIFC15 H20 Cl N OC 1 2/c 117.0047; 6.656; 24.757
90; 92.075; 90
2800.24Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132816 CIFC16 H22 Cl N OP 1 21/c 112.6132; 6.8258; 17.3255
90; 93.319; 90
1489.14Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132817 CIFC17 H18 Cl N OP 21 21 217.6345; 9.6295; 20.4737
90; 90; 90
1505.15Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132818 CIFC13 H18 Cl N OP -16.66649; 9.4285; 10.2117
93.58; 96.362; 93.083
635.47Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132819 CIFC26 H44 B N2 SiP -110.212; 11.708; 12.522
106.885; 100.518; 90.377
1405.7Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132820 CIFC35 H62 B N3 O SiP 1 21/n 110.2572; 18.663; 19.5822
90; 99.642; 90
3695.67Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132821 CIFC66 H96 B2 N4 O2 Si2C 1 2/c 116.1834; 30.376; 17.5363
90; 113.974; 90
7876.9Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132822 CIFC20 H15 Cl3 O2P 1 21/c 110.8147; 9.8903; 16.969
90; 104.319; 90
1758.6Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132823 CIFC24 H16 O2P 1 21/c 112.2366; 17.3994; 8.2782
90; 102.186; 90
1722.8Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132824 CIFC19 H15 Cl OP -19.6677; 12.9019; 13.3368
73.28; 88.509; 71.049
1502.7Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132825 CIFC12 H11 Br2 N3 ZnP -17.8069; 7.8757; 11.9902
77.783; 85.879; 77.735
703.79Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132826 CIFC14 H17 Br2 N3 S ZnP -17.852; 10.8828; 11.3769
75.796; 74.568; 76.283
892.99Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132827 CIFC15 H19 Br2 N3 O S ZnP -17.5172; 10.647; 13.487
105.076; 92.008; 109.849
971.3Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132828 CIFC15 H17 Br2 N3 O S ZnP 1 21/c 17.3412; 19.033; 13.475
90; 98.398; 90
1862.6Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132829 CIFC26 H26 Cl N3 O5P -18.2719; 10.9748; 14.3779
91.073; 98.225; 110.945
1203Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132830 CIFC28.01 H30.01 Br N3 O5P -111.0881; 11.9277; 12.1514
115.124; 105.133; 100.196
1326.22Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132831 CIFC98 H72 Cl4 Cu2 F20 N8P 1 21/c 117.46; 22.68; 14.222
90; 95.69; 90
5604Dong, Yuting; Qian, Long; Chen, Feng; Wang, Yue; Zhang, Tao; Qiu, Fengxian; Teranishi, Toshiharu; Xue, Songlin
Benzene-fused porphyrin(2.1.2.1) array: synthesis, structure, and electrocatalytic hydrogen evolution.
Chemical communications (Cambridge, England), 2024, 60, 3986-3989
7132832 CIFC19 H17 F3 N2 O4 SP b c a19.2019; 13.9245; 28.2926
90; 90; 90
7564.8Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132833 CIFC18 H17 F3 N2 O4 SP b c a19.421; 13.8099; 27.8614
90; 90; 90
7472.49Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132834 CIFC20 H18 N2 O4.5 VP 1 21/c 115.3045; 8.8087; 13.3399
90; 98.687; 90
1777.76Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132835 CIFC55.66 H21.3 Cl3.31 F10 N8 Pd SP 1 21 113.3831; 7.1785; 26.0801
90; 93.166; 90
2501.71Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132836 CIFC45 H29 B Cl3 F4 N3 Pd SP -19.276; 14.42; 15.664
112.75; 91.73; 91.28
1930Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132837 CIFC74 H42 B F20 N3 Pd SP 1 21/n 113.546; 27.1678; 16.8019
90; 99.633; 90
6096.17Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132838 CIFC46 H32 Cl4 F6 N3 P Pd SP 1 21/c 113.77; 16.0819; 19.035
90; 90.479; 90
4215.1Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132839 CIFC55 H29 Cl3 N8 Pd SP -114.7468; 17.6065; 20.521
69.671; 82.618; 65.328
4539.2Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132840 CIFC47 H20.5 Cl0.5 F16 N3 P Pd SP n a 2128.14; 14.513; 20.554
90; 90; 90
8394Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132841 CIFC20 H26 O4I 1 2/a 110.1083; 14.7871; 22.9034
90; 91.199; 90
3422.68Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132842 CIFC18 H24 O2P -19.864; 9.8656; 16.5931
105.165; 97.065; 105.295
1471Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132843 CIFC27 H15 Br O2P 1 21/c 117.7637; 15.582; 7.0233
90; 95.518; 90
1935Nishimoto, Mikey; Uetake, Yuta; Yakiyama, Yumi; Sakurai, Hidehiro
Strain-induced carbon-carbon bond cleavage of bowl-shaped sumanenone.
Chemical communications (Cambridge, England), 2024, 60, 3982-3985
7132844 CIFC14 H11 N3 O2P 21 21 218.1213; 11.1938; 13.6325
90; 90; 90
1239.31Bhattacharjee, Suvam; Hajra, Alakananda
Site-selective direct nitration of 2<i>H</i>-indazoles: easy access to 7-nitroindazoles.
Chemical communications (Cambridge, England), 2024, 60, 4076-4079
7132845 CIFC38 H61 N4 P2 Sc SiP 1 21/c 115.5452; 15.3097; 17.8477
90; 97.496; 90
4211.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132846 CIFC73 H110 N10 Ni2 P4 Sc2P -112.49; 12.54; 13.517
65.861; 73.439; 76.945
1837.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132847 CIFC46 H59 N6 Ni P2 ScP -110.9882; 11.7463; 18.988
74.157; 89.563; 72.84
2245.6Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132848 CIFC43 H57 N4 Ni P2 ScP -111.122; 11.696; 16.447
101.88; 96.172; 90.996
2079.8Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132849 CIFC48 H68 N5 Ni O1.5 P2 ScP -110.142; 10.213; 23.78
77.96; 79.02; 81.49
2350Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132850 CIFC118 H142 N10 Ni2 O2 P4 Sc2C 1 2/c 128.918; 11.542; 36.001
90; 109.45; 90
11330Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132851 CIFC43 H58 N5 Ni P2 ScP -112.237; 13.83; 15.21
68.64; 72.04; 64.89
2134Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132852 CIFC21 H19 N O2P 1 21/c 110.0187; 15.8815; 10.6953
90; 99.728; 90
1677.28Karjee, Pallab; Debnath, Bijoy; Mandal, Santu; Saha, Sharajit; Punniyamurthy, Tharmalingam
One-pot C-N/C-C bond formation and oxidation of donor-acceptor cyclopropanes with tetrahydroisoquinolines: access to benzo-fused indolizines.
Chemical communications (Cambridge, England), 2024, 60, 4068-4071
7132853 CIFC22 H20 O5P 1 21/n 19.08906; 9.90544; 20.1477
90; 92.251; 90
1812.52Nambu, Hisanori; Onuki, Yuta; Aso, Kana; Kanamori, Momoka; Tomohara, Keisuke; Tsuge, Kiyoshi; Yakura, Takayuki
Ring expansion of spirocyclopropanes with stabilized sulfonium ylides: highly diastereoselective synthesis of cyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 4537-4540
7132854 CIFC21 H14 O2P 1 21/c 18.1483; 18.778; 9.9744
90; 98.77; 90
1508.3Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132855 CIFC21 H18 O4P -18.487; 10.1115; 10.5324
91.975; 93.296; 108.179
856.01Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132856 CIFC27 H50 Mn3 N6 O53 P W9P 3 1 c18.9481; 18.9481; 29.4882
90; 90; 120
9168.8Liu, Fangcheng; Han, Shicheng; Dong, Liwei; Fang, Xikui
Functionalized polyoxometalates enable fast ion transport in solid-state batteries at room temperature.
Chemical communications (Cambridge, England), 2024, 60, 4198-4201
7132857 CIFC17 H18 OP 1 21 111.5667; 5.2499; 12.1291
90; 117.369; 90
654.08Wang, Kun; Niu, Saisai; Tang, Weijun; Xue, Dong; Xiao, Jianliang; Li, Hongfeng; Wang, Chao
Ru-catalyzed asymmetric hydrogenation of α,β-unsaturated ketones <i>via</i> a hydrogenation/isomerization cascade.
Chemical communications (Cambridge, England), 2024, 60, 4338-4341
7132858 CIFC30 H45 F5 O2P 1 21 112.4586; 9.2797; 13.4386
90; 105.661; 90
1495.99Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132859 CIFC31 H45 F7 O2P 1 21 112.9607; 8.8159; 13.5926
90; 106.421; 90
1489.74Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132860 CIFC32 H45 F9 O2P 1 21 112.299; 9.2607; 14.5611
90; 94.027; 90
1654.38Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132861 CIFC31 H45 F7 O2P 1 21 112.7803; 9.3254; 13.7005
90; 104.745; 90
1579.07Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132862 CIFC33 H45 F11 O2P 21 21 219.236; 12.542; 29.3792
90; 90; 90
3403.2Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132863 CIFC34 H45 F13 O2P 1 21 113.3455; 8.8735; 14.404
90; 90.499; 90
1705.68Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132864 CIFC44 H53 Ca I N2 O2P 1 21/c 111.1453; 21.6411; 16.4519
90; 99.62; 90
3912.34Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132865 CIFC44 H53 I N2 O2 SrP 1 21/c 111.1365; 21.9592; 16.4408
90; 99.267; 90
3968.1Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132866 CIFC40 H57 N3 O Si2 SrC 1 2/c 122.9542; 9.945; 37.2321
90; 105.936; 90
8172.69Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132867 CIFC35.99 H48.98 Ca N3 Si2C 1 2/c 121.9451; 9.6032; 35.7576
90; 105.893; 90
7247.62Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132868 CIFC88 H64 N16 Pt2C 1 2/m 114.2019; 21.4417; 19.1515
90; 98.888; 90
5761.9van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132869 CIFC100 H80 B4 F16 N16 Pt2P -111.1598; 14.8934; 17.8869
87.192; 75.514; 86.266
2870.67van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132870 CIFC19 H17 Cl N2 O4P -19.6699; 9.6753; 10.4512
76.908; 71.347; 71.318
869.2Porashar, Bikoshita; Behera, Bipin Kumar; Phukon, Hunmoina; Saikia, Anil K.
Synthesis of tetrahydroquinazolines from 2-aminobenzonitriles and alkylidene malonates <i>via</i> 1,4-conjugate addition and an unprecedented rearrangement reaction.
Chemical communications (Cambridge, England), 2024, 60, 4358-4361
7132871 CIFC52 H34.66 Au3 Lu N20 O9.33P b c a19.9815; 23.8662; 23.8919
90; 90; 90
11393.6Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132872 CIFC52 H34.34 Au3 N20 O9.17 TbP b c a20.0668; 23.8472; 23.9197
90; 90; 90
11446.5Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132873 CIFC52 H34.51 Au3 Eu N20 O9.25P b c a20.1041; 23.8591; 23.936
90; 90; 90
11481.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132874 CIFC52 H34.4 Au3 Ce N20 O9.2P b c a20.2203; 23.8559; 23.9799
90; 90; 90
11567.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132875 CIFC19 H16 O4P 1 21/c 110.9362; 17.792; 8.2146
90; 108.127; 90
1519.04Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132876 CIFC20 H22 O5 SC 1 2/c 121.549; 10.8252; 17.856
90; 113.929; 90
3807.3Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132877 CIFC25 H22 O4P 1 21/c 110.2833; 10.038; 20.688
90; 98.406; 90
2112.6Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132878 CIFC16 H19 N O4P 1 21/n 113.824; 7.5535; 14.7562
90; 100.354; 90
1515.75Feng, Shishen; Liu, Hong; Li, Yan; Fang, Yewen
Photoredox-catalyzed radical-radical cross coupling of ketyl radicals with unstabilized primary alkyl radicals.
Chemical communications (Cambridge, England), 2024, 60, 4431-4434
7132879 CIFC57 H43 Au Br Cl18 Fe N6 OC m m m20.0212; 28.7967; 16.6677
90; 90; 90
9609.7Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132880 CIFC57 H43 Au Br Cl18 Fe N6 OP m m m10.4824; 14.6177; 17.0399
90; 90; 90
2611Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132881 CIFC88 H140 Co Fe N17 O19P m m m10.218; 14.6762; 17.0726
90; 90; 90
2560.2Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132882 CIFC83 H118 Fe2 N16 O15C m m m19.818; 29.05; 16.4847
90; 90; 90
9490.5Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132883 CIFC83 H118 Fe2 N16 O15C m m m20.623; 29.23; 17.01
90; 90; 90
10253.8Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132884 CIFC18 H13 N O3P b c a11.248; 11.9893; 21.1722
90; 90; 90
2855.19Liao, Zhi-Yu; Gao, Fan; Ye, Yu-Hang; Yu, Qian-Hui; Yang, Cui; Luo, Qing-Yu; Du, Fei; Pan, Bin; Zhong, Wen-Wu; Liang, Wu
Construction of cyclobutane-fused tetracyclic skeletons <i>via</i> substrate-dependent EnT-enabled dearomative [2+2] cycloaddition of benzofurans (benzothiophenes)/maleimides.
Chemical communications (Cambridge, England), 2024, 60, 4455-4458
7132885 CIFC21 H23 N O3 SP 1 21 110.5669; 8.0829; 11.7127
90; 113; 90
920.87Li, Hongye; Zhou, Yuqiao; Tan, Zheng; Wang, Xiangyu; Zhang, Yuxin; Wang, Fei; Feng, Xiaoming; Liu, Xiaohua
Enantioselective sulfonylation to construct 3-sulfonylated oxindoles.
Chemical communications (Cambridge, England), 2024, 60, 4354-4357
7132886 CIFC20 H16 Br N OP 1 21/c 110.887; 13.619; 11.857
90; 110.116; 90
1650.8Solanke, Pooja R.; Kumar, Prakash; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Synthesis of <i>cis</i>-fused cyclopentenone-pyrrolidine scaffolds <i>via</i> sequential aza-Piancatelli and Conia-ene type reactions in one pot.
Chemical communications (Cambridge, England), 2024, 60, 4234-4237
7132887 CIFC26 H21 N OP 1 n 18.577; 16.525; 29.33
90; 98.477; 90
4112Solanke, Pooja R.; Kumar, Prakash; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Synthesis of <i>cis</i>-fused cyclopentenone-pyrrolidine scaffolds <i>via</i> sequential aza-Piancatelli and Conia-ene type reactions in one pot.
Chemical communications (Cambridge, England), 2024, 60, 4234-4237
7132888 CIFC58 H46 O10I 1 2/a 17.6531; 20.7577; 37.5707
90; 92.335; 90
5963.6Zhang, Qiaoyu; Luo, Guiwen; Hu, Rui; Yang, Guoqiang; Chen, Jinping; Yu, Tianjun; Zeng, Yi; Li, Yi
Crystalline hydrogen-bonded organic framework for air-tolerant triplet-triplet annihilation upconversion.
Chemical communications (Cambridge, England), 2024, 60, 4475-4478
7132889 CIFC16 H21 N O2C 1 2/c 121.9697; 6.3504; 23.532
90; 114.886; 90
2978.3Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132890 CIFC24 H41 N O4P 21 21 216.372; 21.111; 17.2221
90; 90; 90
2316.7Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132891 CIFC32 H42 N2 O4P -15.6228; 11.5801; 22.772
88.886; 84.246; 83.434
1465.5Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132892 CIFC24 H39 N O3P 21 21 2110.4856; 14.332; 14.635
90; 90; 90
2199.3Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132893 CIFC35 H41 Cl4 O P RuP 1 21 110.0658; 15.252; 11.7038
90; 110.346; 90
1684.71Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132894 CIFC15 H19 Br N2 O2P 1 21 17.049; 11.48; 19.45
90; 98.623; 90
1556.2Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132895 CIFC28 H40 Cl4 Ru2P 1 21/c 112.2863; 18.7694; 12.3374
90; 93.047; 90
2841.06Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132896 CIFC46 H55 Cl2 N2 O2 SbC 1 c 120.0826; 14.1346; 15.2463
90; 100.815; 90
4250.9Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132897 CIFC49 H62 Cl N2 O4 SbP 1 21/c 124.3993; 16.832; 11.663
90; 100.297; 90
4712.7Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132898 CIFC46 H57 N2 O4 SbP b c a28.4574; 27.9101; 32.3437
90; 90; 90
25688.9Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132899 CIFC31 H37 N O3 S SiP -19.462; 9.6433; 17.6776
75.612; 75.789; 87.111
1514.5Zhang, Zhen; Lu, Lichao; Li, Guiling; Sheng, Xiaoyu; Zhang, Yijia; Yang, Lin; Zhao, Jiaqi; Xie, Lei; Li, Jiazhu; Sun, Kai
Radical cascade silylation/cyclization of 1,7-dienes to access silyl-substituted benzo[<i>b</i>]azepin-2-ones.
Chemical communications (Cambridge, England), 2024, 60, 4206-4209
7132900 CIFC17 H10 N2P 21 21 214.5044; 12.6636; 19.6473
90; 90; 90
1120.72Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132901 CIFC24 H14 N2 OP -17.6716; 9.16801; 12.73071
106.171; 91.1629; 109.967
801.64Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132902 CIFC25 H14 N2P 21 21 215.7818; 12.8402; 21.6872
90; 90; 90
1610.05Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132903 CIFC17 H12 N2 OC 1 2/c 116.3278; 7.4345; 21.1425
90; 99.071; 90
2534.37Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132904 CIFC23 H16 N2 OP 1 21/c 112.43235; 12.20419; 11.52302
90; 102.48; 90
1707.04Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132905 CIFC17 H9 N3 OP 1 21/c 13.77916; 16.2226; 19.1757
90; 93.565; 90
1173.35Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132906 CIFC23 H16 N2 OP -18.22512; 10.0169; 12.1195
104.088; 101.613; 109.165
870.66Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132907 CIFC19 H12 N2P 1 21/n 117.6032; 3.8528; 18.9019
90; 99.58; 90
1264.08Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132908 CIFC18 H21 N O6P 1 21/c 111.5445; 11.4051; 12.9631
90; 93.189; 90
1704.16Wen, Yongshun; Jin, Hong-Xian; Qiu, Yan-Hua; Zong, Yingtong; Luo, Wenjun; Chen, Zhengwang; Yu, Daohong
Photo-induced tungsten-catalyzed cascade synthesis of pyrrolo[2,1-<i>a</i>]isoquinoline-1,3-dicarboxylate and its reaction mechanism.
Chemical communications (Cambridge, England), 2024, 60, 4573-4576
7132909 CIFC44 H44 O10P -115.186; 15.823; 16.474
69.815; 88.884; 81.886
3676.4Soliman, Luc; Ramassamy, Elsa; Dujarric, Katia; Naulet, Guillaume; Dechambenoit, Pierre; Bock, Harald; Durola, Fabien
Coronenes with push-pull geometries from macrocycle-forming Perkin condensations.
Chemical communications (Cambridge, England), 2024, 60, 4439-4442
7132910 CIFC36 H28 O8P -16.9314; 13.781; 16.068
86.662; 82.997; 76.021
1477.62Soliman, Luc; Ramassamy, Elsa; Dujarric, Katia; Naulet, Guillaume; Dechambenoit, Pierre; Bock, Harald; Durola, Fabien
Coronenes with push-pull geometries from macrocycle-forming Perkin condensations.
Chemical communications (Cambridge, England), 2024, 60, 4439-4442
7132911 CIFC38 H38 B Cl4 F6 N S SbP c c n8.895; 16.5456; 27.257
90; 90; 90
4011.5Cosby, Taylor P. L.; Bhattacharjee, Avik; Henneberry, Samantha K.; LeBlanc, Jesse; Caputo, Christopher B.
Unlocking Lewis acidity <i>via</i> the redox non-innocence of a phenothiazine-substituted borane.
Chemical communications (Cambridge, England), 2024, 60, 5391-5394
7132912 CIFC20 H14 N2 O6 WC 1 2/c 116.6532; 10.7273; 11.4809
90; 103.498; 90
1994.3Song, Heng; Xiao, Yuting; Wei, Jingjing; Liu, Yuzan; Yang, Liqing; Bai, Pengtao; Yang, Fu; Yu, Kai; Xu, Chen; Cai, Xingwei
Low-valent-tungsten catalysis enables hydroboration of esters and nitriles.
Chemical communications (Cambridge, England), 2024, 60, 5026-5029
7132913 CIFC10 H14 Br4 F N2 ZnP 1 21/c 18.0955; 20.9526; 9.8012
90; 102.25; 90
1624.64Wang, Yu-Yin; Kang, Huai-Yuan; Zhang, Shao-Ya; Qu, Hao; Zhu, Lin; Zhao, Dan; Li, Xian-Feng; Lei, Xiao-Wu; Yue, Cheng-Yang
Exploring 0D lead-free metal halide with highly efficient blue light emission and high-sensitivity photodetection.
Chemical communications (Cambridge, England), 2024, 60, 2784-2787
7132914 CIFC21 H28 Cl2 Co N3P 1 21/n 110.4791; 15.9525; 12.9626
90; 99.6049; 90
2136.55Boity, Biswaranjan; Sidiqque, Misba; Rit, Arnab
Amine-functionalized bifunctional Co<sup>III</sup>-NHC complexes: highly effective phosphine-free catalysts for the α-alkylation of nitriles.
Chemical communications (Cambridge, England), 2024, 60, 3142-3145
7132915 CIFC16 H11 N3 OP 21 21 213.741; 17.187; 18.371
90; 90; 90
1181.19Sarkar, Souradip; Bhunya, Sourav; Pan, Subarna; Datta, Arnadeep; Roy, Lisa; Samanta, Rajarshi
Rh(II)-catalysed <i>N</i><sup>2</sup>-selective arylation of benzotriazoles and indazoles using quinoid carbenes <i>via</i> 1,5-H shift.
Chemical communications (Cambridge, England), 2024, 60, 4727-4730
7132916 CIFC17 H12 N2 OP b c a11.511; 10.247; 21.356
90; 90; 90
2519Sarkar, Souradip; Bhunya, Sourav; Pan, Subarna; Datta, Arnadeep; Roy, Lisa; Samanta, Rajarshi
Rh(II)-catalysed <i>N</i><sup>2</sup>-selective arylation of benzotriazoles and indazoles using quinoid carbenes <i>via</i> 1,5-H shift.
Chemical communications (Cambridge, England), 2024, 60, 4727-4730
7132917 CIFC31 H29 N O5P -110.8447; 11.198; 12.0881
101.529; 90.637; 113.153
1315.93Pramanik, Sourav; Hazra, Subhadeep; Chatterjee, Ayan; Saha, Jaideep
Hydrogen bonding-promoted tunable approach for access to aza-bicyclo-[3.3.0]octanes and cyclopenta[<i>b</i>] pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 4922-4925
7132918 CIFC56 H40 As4 Cl4 Cu4 Mo8 O16 Sb4P -115.055; 15.1827; 17.1422
89.358; 89.116; 69.16
3661.4Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132919 CIFC15 H12 As Cl2 Cu I Mo2 O4 SbP 1 21/n 110.4347; 15.6404; 13.4725
90; 92.374; 90
2196.86Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132920 CIFC56 H40 As4 Br4 Cu4 Mo8 O16 Sb4P -114.9733; 15.0851; 17.339
89.022; 88.933; 70.588
3692.9Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132921 CIFC67 H25 Al As2 Cl2 Cu F46 Mo4 N O11 Sb2P 1 21/c 120.9582; 33.303; 12.1289
90; 105.237; 90
8168.03Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132922 CIFC129 H42 Ag2 Al2 As4 Cl2 F92 Mo8 O22 Sb4P 1 21/n 111.4664; 40.5323; 33.5837
90; 91.704; 90
15601.4Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132923 CIFC108.8 H34.6 Al2 As2 Cl5.6 Cu2 F92 Mo4 N3 O14 Sb2P 1 21/n 123.6343; 19.0078; 31.4538
90; 98.5123; 90
13974.5Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132924 CIFC30 H30 Si3P 1 21/c 19.9325; 18.2411; 15.0008
90; 102.356; 90
2654.89Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132925 CIFC37 H37 N3 Si3P 1 21/c 112.98096; 26.6317; 10.50266
90; 91.5598; 90
3629.48Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132926 CIFC32 H36 Si4P 1 21/c 124.3501; 11.0409; 25.4353
90; 115.708; 90
6161.3Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132927 CIFC35 H25 N O2 SP -18.8511; 10.7751; 14.2389
81.33; 88.876; 74.316
1292.16Malik, Nirmal; De, Ritobrata; Pal, Santanu Kumar; Ramasastry, S. S. V.
A one-pot telescopic synthesis of benzo[<i>b</i>]carbazoles and exploration of their liquid crystalline properties.
Chemical communications (Cambridge, England), 2024, 60, 4797-4800
7132928 CIFC90 H80 B2 N6 Ni2 O4C 1 2/c 132.431; 24.9205; 24.931
90; 123.299; 90
16841Patra, Suman; Atta, Sayan; Ghosh, Soumili; Majumdar, Amit; Dey, Abhishek
Kinetic isotope effect offers selectivity in CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 4826-4829
7132929 CIFC19 H22 Cl N3 Ni O7P 1 21/c 19.1074; 16.575; 14.4535
90; 107.064; 90
2085.8Patra, Suman; Atta, Sayan; Ghosh, Soumili; Majumdar, Amit; Dey, Abhishek
Kinetic isotope effect offers selectivity in CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 4826-4829
7132930 CIFC62 H66 N6 O17 P4 U2C 1 2/c 131.0258; 12.8733; 16.8307
90; 114.157; 90
6133.6Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132931 CIFC28 H26 N2 O2 P2P 1 21/c 110.1143; 28.2649; 8.4249
90; 98.202; 90
2383.87Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132932 CIFC56 H52 N10 O28 P4 U3P 1 21/c 119.1125; 10.6852; 17.9947
90; 107.716; 90
3500.6Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132933 CIFC28 H26 N2 O2 P2P -18.231; 11.7984; 13.6524
73.829; 85.363; 76.865
1239.83Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132934 CIFC72 H98 S2 TmP -113.2573; 14.2636; 18.3627
104.34; 93.693; 98.57
3307.9Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132935 CIFC72 H98 I Nd S2P -113.3492; 14.1047; 18.6556
102.433; 94.721; 99.287
3360.2Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132936 CIFC72 H98 Nd S2P -113.2169; 14.2162; 18.5245
104.917; 93.8221; 97.9184
3312.3Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132937 CIFC72 H98 I La S2P -113.2786; 14.2335; 18.678
102.71; 94.255; 99.004
3379.5Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132938 CIFC72 H98 I0.13 La S2P -113.209; 14.2623; 18.5499
104.544; 93.628; 98.433
3327.73Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132939 CIFC84 H108 N2 S2 SmP b c n16.0032; 18.7417; 24.3011
90; 90; 90
7288.6Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132940 CIFC84 H108 N2 Nd S2P b c n15.9566; 18.7918; 24.254
90; 90; 90
7272.6Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132941 CIFC17 H22 N2 O2 SP 1 21 110.9048; 14.2184; 11.9956
90; 110.377; 90
1743.51Wei, Tao; Xie, Ming-Sheng; Guo, Hai-Ming
Construction of thioglycoside bonds <i>via</i> an asymmetric organocatalyzed sulfa-Michael/aldol reaction: access to 4'-thionucleosides.
Chemical communications (Cambridge, England), 2024, 60, 5018-5021
7132942 CIFC23 H18 N2 O SP 1 21/n 18.252; 14.7387; 15.4992
90; 96.548; 90
1872.8Wang, Xinxin; Wang, Jie; Ji, Meishan; Wu, Xinxin; Zhu, Chen
<i>Z</i>-selective radical difunctionalization of aromatic alkynes: synthesis of multi-substituted triarylethenes.
Chemical communications (Cambridge, England), 2024, 60, 4894-4897
7132943 CIFC23 H16 F N O SC 1 2/c 112.5347; 15.7748; 19.3093
90; 98.0108; 90
3780.8Wang, Xinxin; Wang, Jie; Ji, Meishan; Wu, Xinxin; Zhu, Chen
<i>Z</i>-selective radical difunctionalization of aromatic alkynes: synthesis of multi-substituted triarylethenes.
Chemical communications (Cambridge, England), 2024, 60, 4894-4897
7132944 CIFC100 H86 N2 O32 P4 W10P -113.5793; 15.3135; 15.4699
117.216; 113.848; 92.658
2508.49Gu, Chen; Yatabe, Takafumi; Yamaguchi, Kazuya; Suzuki, Kosuke
Photocatalytic aerobic α-oxygenation of amides to imides using a highly durable decatungstate tetraphenylphosphonium salt.
Chemical communications (Cambridge, England), 2024, 60, 4906-4909
7132945 CIFC41.5 H21.5 Cl0.25 N5 O5.5P 1 21/m 112.7611; 18.5038; 14.1018
90; 100.643; 90
3272.56Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132946 CIFC81.46 H39.92 Cl0.92 N9 O6I 1 2/a 130.8326; 13.5754; 31.1005
90; 106.96; 90
12451.4Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132947 CIFC153 H47 Cl4 N9 O6P 1 21/n 113.0791; 32.0488; 27.0224
90; 94.916; 90
11285.3Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132948 CIFC163 H47 Cl4 N9 O6P 1 21/n 126.5926; 32.943; 30.1206
90; 113.007; 90
24288Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132949 CIFC20 H6 Cl8 NP 1 21/c 114.0305; 8.0731; 18.9296
90; 94.608; 90
2137.2Lv, Kuo; Zhang, Minzhe; Xia, Xin; Liu, Wenjing; Wan, Keke; Zhang, Ming; Li, Feng
Cyano modified triphenylmethyl radical skeletons: higher stability and efficiency.
Chemical communications (Cambridge, England), 2024, 60, 4846-4849
7132950 CIFC21 H6 Cl7 N2P -18.2197; 11.2036; 13.6336
67.189; 84.761; 73.004
1106.4Lv, Kuo; Zhang, Minzhe; Xia, Xin; Liu, Wenjing; Wan, Keke; Zhang, Ming; Li, Feng
Cyano modified triphenylmethyl radical skeletons: higher stability and efficiency.
Chemical communications (Cambridge, England), 2024, 60, 4846-4849
7132951 CIFC26 H22 Cl N O2P -17.7575; 11.8553; 12.4714
68.379; 88.015; 75.886
1032.14Sui, Jia-Li; Zhong, Long-Jin; Xiong, Bi-Quan; Tang, Ke-Wen; Liu, Yu
Regioselective synthesis of N-containing polycyclic compounds <i>via</i> radical annulation cyclization of 1,7-dienes with aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 4834-4837
7132952 CIFC16 H19 N O2P 1 21/c 116.3685; 10.1416; 33.0222
90; 92.147; 90
5477.93Liu, Zhaosheng; Ji, Xiaochen; Duan, Lilan; Deng, Guo-Jun; Huang, Huawen
Accessing pyrrolo[1,2-<i>a</i>]indole derivatives <i>via</i> visible-light-induced dearomatizative cyclization of indoles.
Chemical communications (Cambridge, England), 2024, 60, 4902-4905
7132953 CIFC13 H15 N O2P 1 21/c 119.4445; 8.085; 15.4094
90; 111.936; 90
2247.1Liu, Zhaosheng; Ji, Xiaochen; Duan, Lilan; Deng, Guo-Jun; Huang, Huawen
Accessing pyrrolo[1,2-<i>a</i>]indole derivatives <i>via</i> visible-light-induced dearomatizative cyclization of indoles.
Chemical communications (Cambridge, England), 2024, 60, 4902-4905
7132954 CIFC40 H36 N2 O2P -112.0197; 12.0255; 13.0084
87.125; 64.484; 67.794
1556.7Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132955 CIFC43 H43 N2 O2P 112.3589; 12.8347; 22.1604
79.4229; 87.2486; 87.6565
3449.59Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132956 CIFC43 H43 N2 O2P 112.3589; 12.8455; 22.1587
79.4344; 87.2227; 87.6319
3452.24Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132957 CIFC18 H17 N O2P 1 21/c 16.3783; 7.1006; 31.5404
90; 93.88; 90
1425.18Gao, Ying; Wang, Mingxu; Sun, Jingxian; Zhao, Xiao-Jing; He, Yonghui
Electrochemical-induced solvent-tuned selective C(sp<sup>3</sup>)-H bond activation towards the synthesis of C3-functionalized chromone derivatives.
Chemical communications (Cambridge, England), 2024, 60, 5050-5053
7132958 CIFC50 H45 B2 F4 N5 O2P -112.912; 16.473; 22.588
71.34; 83.507; 79.792
4471.7Wang, Long; Cheng, Cheng; Yu, Changjiang; Wu, Qinghua; Kang, Zhengxin; Wang, Hua; Jiao, Lijuan; Hao, Erhong
NIR-absorbing and emitting α,α-nitrogen-bridged BODIPY dimers with strong excitonic coupling.
Chemical communications (Cambridge, England), 2024, 60, 5054-5057
7132959 CIFC17 H14 F N OP n a 2112.4495; 20.4914; 5.0901
90; 90; 90
1298.52Liu, Hongxin; Tang, Tingyu; Li, Bin; Wang, Baiquan
Manganese(I)-catalyzed nucleophilic addition of C(sp<sup>3</sup>)-H bonds to aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 5066-5069
7132960 CIFC14 H8 Mn N O4P 1 21/n 17.631; 8.00772; 20.9823
90; 98.411; 90
1268.37Liu, Hongxin; Tang, Tingyu; Li, Bin; Wang, Baiquan
Manganese(I)-catalyzed nucleophilic addition of C(sp<sup>3</sup>)-H bonds to aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 5066-5069
7132961 CIFC34 H34 S2R -3 :H37.256; 37.256; 5.1212
90; 90; 120
6155.9Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132962 CIFC30 H22 SP 1 21/c 114.9168; 5.1215; 80.8465
90; 92.323; 90
6171.3Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132963 CIFC27 H24 SP -112.0192; 13.1986; 13.5978
91.326; 92.661; 113.371
1975.96Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132964 CIFC19 H19 F3 N2P 1 21/c 110.34; 15.24; 11.008
90; 94.938; 90
1728.2Yang, Ming; Meng, Yu-Xuan; Mehfooz, Haroon; Zhao, Yu-Long
Visible light-promoted [3+2] cyclization reaction of vinyl azides with perfluoroalkyl-substituted-imidoyl sulfoxonium ylides.
Chemical communications (Cambridge, England), 2024, 60, 5407-5410
7132965 CIFC34 H33 N O2P 1 21/c 121.901; 11.9356; 10.1958
90; 95.864; 90
2651.3Pramanik, Shyamal; Samanta, Apurba; Maity, Soumitra
A two carbon homologation of Friedel-Crafts alkylation enabled by photochemical alkene stitching: modular assembly of cyclolignans.
Chemical communications (Cambridge, England), 2024, 60, 5282-5285
7132966 CIFC22 H26 O6P 1 21/c 113.0879; 11.0775; 14.0938
90; 102.597; 90
1994.1Pramanik, Shyamal; Samanta, Apurba; Maity, Soumitra
A two carbon homologation of Friedel-Crafts alkylation enabled by photochemical alkene stitching: modular assembly of cyclolignans.
Chemical communications (Cambridge, England), 2024, 60, 5282-5285
7132967 CIFC18 H16 N12 O8 S Zn3P 1 21/c 114.143; 9.9829; 25.111
90; 96.777; 90
3520.6Deng, Yu-Xin; Yang, Guo-Ping; Wang, Yao-Yu
Pure separation of acetylene based on a sulfonic acid and amino group functionalized Zn-MOF.
Chemical communications (Cambridge, England), 2024, 60, 5046-5049
7132968 CIFC18 H14 N12 O7 S Zn3P 1 21/c 114.0795; 9.851; 25.9541
90; 95.909; 90
3580.6Deng, Yu-Xin; Yang, Guo-Ping; Wang, Yao-Yu
Pure separation of acetylene based on a sulfonic acid and amino group functionalized Zn-MOF.
Chemical communications (Cambridge, England), 2024, 60, 5046-5049
7132969 CIFC32 H28 Cl2 O8P -19.951; 10.5842; 14.9945
96.395; 99.389; 117.914
1344.5Kelsey, Shaun R.; Griaznov, Georgii; Spaeth, Andrew D.; Janzen, Daron E.; Douglas, Justin T.; Thompson, Ward H.; Barybin, Mikhail V.
Tuning the redox profile of the 6,6'-biazulenic platform through functionalization along its molecular axis.
Chemical communications (Cambridge, England), 2024, 60, 5213-5216
7132970 CIFFe Nb Te2P 1 21/c 17.28; 6.305; 7.992
90; 92.33; 90
366.5Stepanova, Anna V.; Mironov, Andrei V.; Bogach, Alexey V.; Azarevich, Andrey N.; Presniakov, Igor A.; Sobolev, Alexey V.; Pankratov, Denis A.; Zayakhanov, Vladimir A.; Starchikov, Sergey S.; Verchenko, Valeriy Yu; Shevelkov, Andrei V.
Bulk ferromagnetism in cleavable van der Waals telluride NbFeTe<sub>2</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5518-5521
7132971 CIFC52 H46 F3 Fe N3 P2P -111.711; 12.5996; 16.8271
96.344; 100.608; 116.094
2139.53Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132972 CIFC48 H50 Fe N4 P2P -110.7765; 13.6127; 14.6156
90.015; 96.865; 100.703
2091.1Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132973 CIFC60 H52 F6 Fe N2 O P2P -113.4659; 13.8415; 14.7796
93.409; 105.088; 106.332
2526.2Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132974 CIFC78 H64 F4 Fe N2 P2C 1 2/c 129.4666; 13.8824; 16.5411
90; 114.212; 90
6171.2Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132975 CIFC26 H20 N2 O3I 1 2/a 115.6096; 16.4461; 16.1674
90; 96.743; 90
4121.74Zhao, Shuang; Chen, Mengxiao; Zhou, Wenlu; Ni, Dan; Li, Zhenghua; Nie, Shenyou; He, Yi
Green synthesis for diverse bioactive benzo-fused spiroindolines through DBU-catalysed post-Ugi double cyclization.
Chemical communications (Cambridge, England), 2024, 60, 5455-5458
7132976 CIFC28 H18 N2 O4P -110.0719; 10.5354; 10.8948
92.2576; 111.172; 93.0417
1074.38Akbari, Alireza; Khosravi, Hormoz; Bauer, Felix; Rominger, Frank; Breit, Bernhard; Balalaie, Saeed
Metal- and solvent-free domino reaction of 2-isocyanophenol esters to benzoxazines: long-range 1,5-acyl migration on 1,4-diazabutatriene.
Chemical communications (Cambridge, England), 2024, 60, 5451-5454
7132977 CIFC16 H13 N O3P -16.7066; 8.7863; 12.6844
100.298; 96.3058; 111.389
672.14Akbari, Alireza; Khosravi, Hormoz; Bauer, Felix; Rominger, Frank; Breit, Bernhard; Balalaie, Saeed
Metal- and solvent-free domino reaction of 2-isocyanophenol esters to benzoxazines: long-range 1,5-acyl migration on 1,4-diazabutatriene.
Chemical communications (Cambridge, England), 2024, 60, 5451-5454
7132978 CIFC97 H203 Ag45 Nb6 O47 S23P b c a28.7435; 28.3372; 48.7703
90; 90; 90
39723.9Zhao, Zichen; Zhao, Mengyun; Deng, Lan; Li, Qing; Zhang, Jing; Su, Haifeng; Lv, Hongjin; Yang, Guo-Yu
Two structurally new Lindqvist hexaniobate-templated silver thiolate clusters.
Chemical communications (Cambridge, England), 2024, 60, 5415-5418
7132979 CIFC82 H210 Ag41 K Nb6 O42.5 S26.5P 42 21 232.1512; 32.1512; 17.6732
90; 90; 90
18268.8Zhao, Zichen; Zhao, Mengyun; Deng, Lan; Li, Qing; Zhang, Jing; Su, Haifeng; Lv, Hongjin; Yang, Guo-Yu
Two structurally new Lindqvist hexaniobate-templated silver thiolate clusters.
Chemical communications (Cambridge, England), 2024, 60, 5415-5418
7132980 CIFC32 H72 Cu2 I4 P2P -112.4248; 12.9746; 16.828
86.253; 75.221; 64.491
2364.3Delafoulhouze, Jérémy; Cordier, Marie; Mevellec, Jean-Yves; Massuyeau, Florian; Hernandez, Olivier; Latouche, Camille; Perruchas, Sandrine
Mechanoresponsive luminescence triggered by phase transition of a supercooled copper(I) complex.
Chemical communications (Cambridge, England), 2024, 60, 5278-5281
7132981 CIFC8 H3 O5 TiI 41 2 215.1203; 15.1203; 11.9863
90; 90; 90
2740.35Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132982 CIFC8 H3 D1.25 N0.42 O5 TiI 41 2 215.0507; 15.0507; 12.0595
90; 90; 90
2731.8Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132983 CIFC8 H3 D3.82 N1.27 O5 TiI 41 2 214.92; 14.92; 12.1536
90; 90; 90
2705.47Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132984 CIFC36 H32 N2 O11 Pb2P 1 21/n 116.46; 11.3441; 19.5207
90; 94.325; 90
3634.6Luo, Qi; Li, Yuxia; Huang, Xin; Zheng, Yi; Gu, Qi; Wang, Shuaihua; Wu, Shaofan
Tetraphenylene-based semiconductive metal-organic framework crystals for direct X-ray detection and imaging.
Chemical communications (Cambridge, England), 2024, 60, 5510-5513
7132985 CIFC19 H15 Cl2 N O3P 1 21/c 116.1234; 11.9822; 8.9939
90; 94.945; 90
1731.1Harsha, ?; Kumar, Rohit; Jain, Nidhi
<sup>1</sup>O<sub>2</sub> mediated synthesis of carbonyl substituted quinoline-2,4(1<i>H</i>,3<i>H</i>)-diones in visible light: 4CzIPN as a reusable photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 5646-5649
7132986 CIFC148 H188 F12 Fe2 N18 O28 S4P 1 21/m 116.4651; 23.3184; 17.2067
90; 97.467; 90
6550.3Mobili, Riccardo; Preda, Giovanni; Dondi, Daniele; Monzani, Enrico; Vadivel, Dhanalakshmi; Massera, Chiara; Pasini, Dario; Amendola, Valeria
Triptycene-based diiron(II) mesocates: spin-crossover in solution.
Chemical communications (Cambridge, England), 2024, 60, 5522-5525
7132987 CIFC246 H340 F12 N34 O33 P2P -121.5297; 24.7451; 29.6954
109.868; 104.145; 101.331
13733.1Huang, Song; Wang, Zhenwen; Wu, Jinyang; Mai, Xinyan; Qin, Song; Zhou, Yuqiao; Yuan, Daqiang; Li, Xiaowei; Feng, Wen; Yuan, Lihua
A molecular sheaf: doubly threaded [6]rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 5622-5625
7132988 CIFC16 H24 Au B3 F12 N8C 1 2/c 115.3073; 15.711; 22.0225
90; 99.885; 90
5217.63Barwise, Lachlan; Moon, Lachlan J.; Dhakal, Bibidh; Hogan, Conor F.; White, Keith F.; Dutton, Jason L.
An extremely electron poor Au(III) trication bearing acetonitrile ligands.
Chemical communications (Cambridge, England), 2024, 60, 5586-5589
7132989 CIFC21 H29 Au B2 F8 N6P 1 21 19.4083; 19.422; 15.7483
90; 103.473; 90
2798.46Barwise, Lachlan; Moon, Lachlan J.; Dhakal, Bibidh; Hogan, Conor F.; White, Keith F.; Dutton, Jason L.
An extremely electron poor Au(III) trication bearing acetonitrile ligands.
Chemical communications (Cambridge, England), 2024, 60, 5586-5589
7132990 CIFC198 H251 N6 O46P 1 21/n 122.4005; 26.9673; 32.2242
90; 90.916; 90
19463.5Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132991 CIFC152.46 H189.38 N6 O23.23 S13.23P -121.1953; 26.1285; 31.3285
73.564; 72.242; 68.045
15042Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132992 CIFC190 H208 N6 O58C 1 2/c 139.4383; 27.5839; 35.2015
90; 109.998; 90
35985.4Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132993 CIFC174 H256 N6 O34 S24P 63 2 219.9064; 19.9064; 33.451
90; 90; 120
11479.6Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132994 CIFC138 H148 N6 O16 S6P -121.6989; 27.1612; 27.6258
94.1928; 111.564; 109.903
13867Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132995 CIFC342 H393 N12 O80.01P -121.4803; 27.0745; 29.3858
94.133; 108.263; 112.968
14568.6Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132996 CIFC154.5 H176.5 N15.5 O19.5P -121.6013; 27.1502; 28.3933
93.864; 111.256; 110.441
14178.7Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132997 CIFC132 H130 N6 O13 S3I 1 2 151.7627; 21.7575; 57.0058
90; 90.443; 90
64199.5Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132998 CIFC17 H10 F5 N3P 1 21/c 114.4065; 6.1767; 17.7705
90; 109.917; 90
1486.72Das, Animesh; Maji, Biplab
Substrate-controlled divergent remote C-H and N-H polyfluoroarylation of 2-aminopyrimidines with polyfluoroarenes <i>via</i> Pd(II)/Pd(0) catalysis.
Chemical communications (Cambridge, England), 2024, 60, 5630-5633
7132999 CIFC15 H14 F5 N3P 1 21/c 112.4951; 7.6806; 16.1712
90; 108.511; 90
1471.65Das, Animesh; Maji, Biplab
Substrate-controlled divergent remote C-H and N-H polyfluoroarylation of 2-aminopyrimidines with polyfluoroarenes <i>via</i> Pd(II)/Pd(0) catalysis.
Chemical communications (Cambridge, England), 2024, 60, 5630-5633
7133000 CIFC20 H20 Cl4 N4 NpC 1 2/c 119.2449; 9.5303; 15.6081
90; 127.522; 90
2270.4Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133001 CIFC8 H12 Cl4 N4 NpC 1 2/c 114.6308; 8.4327; 13.7095
90; 91.687; 90
1690.71Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133002 CIFC36 H30 Cl4 Np O2 P2P 1 21 19.9552; 15.3552; 11.9194
90; 98.955; 90
1799.84Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133003 CIFC45.76 H67.53 Cl4 N4 Np O2.44P 1 21/n 116.6555; 11.535; 25.751
90; 94.5345; 90
4931.8Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133004 CIFC18 H20 O3C 1 2/c 133.38; 5.972; 18.656
90; 119.978; 90
3221Kumar, Rakesh; Dutt, Shiv; Banerjee, Prabal
Electrochemical oxidative C-C bond cleavage of methylenecyclopropanes with alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4246-4249
7133005 CIFC23 H22 N2 OP c a 2110.0123; 18.3467; 10.107
90; 90; 90
1856.58Kumar, Dharmendra; Unnikrishnan, Urmila; Kuram, Malleswara Rao
Facile access to <i>C</i>-substituted piperazin-2-ones and mianserin derivative enabled by chemoselective carbene insertion and cyclization cascade.
Chemical communications (Cambridge, England), 2024, 60, 5691-5694
7133006 CIFC9 H19 F3 N2 O4 S2P 1 21/c 19.52; 8.588; 18.645
90; 99.465; 90
1503.6Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133007 CIFC9 H17 F3 N2 O4 S2P 1 21/c 18.664; 9.443; 17.044
90; 95.637; 90
1387.7Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133008 CIFC10 H16 F3 N3 O4 S2P -19.869; 17.149; 18.682
93.615; 92.206; 94.036
3145Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133009 CIFC45 H36 O9P b c m16.1779; 7.77835; 27.1947
90; 90; 90
3422.11Han, Ying; Guo, Wei-Chen; Du, Xu-Sheng; Chen, Chuan-Feng
Synthesis and properties of an <i>O</i>-doped aromatic belt.
Chemical communications (Cambridge, England), 2024, 60, 5719-5722
7133010 CIFC39 H18 O3P 1 21/n 111.4275; 15.9886; 16.0325
90; 97.391; 90
2904.96Han, Ying; Guo, Wei-Chen; Du, Xu-Sheng; Chen, Chuan-Feng
Synthesis and properties of an <i>O</i>-doped aromatic belt.
Chemical communications (Cambridge, England), 2024, 60, 5719-5722
7133011 CIFC58 H41 N3P 21 21 2112.7061; 14.0855; 23.6488
90; 90; 90
4232.5Sharma, Priyank Kumar; Jana, Palash; Bandyopadhyay, Subhajit; Das, Soumyajit
Cyano disubstituted tetrabenzoindeno[2,1-<i>a</i>]fluorene: open-shell or closed-shell?
Chemical communications (Cambridge, England), 2024, 60, 7319-7322
7133012 CIFC27 H42 N4 O5 SiP 1 21/c 112.838; 15.169; 15.0877
90; 102.909; 90
2863.91Jeanmard, Laksamee; Lodovici, Giacomo; George, Ian; Bray, Joshua T. W.; Whitwood, Adrian C.; Thomas, Gavin H.; Fairlamb, Ian J. S.; Unsworth, William P.; Clarke, Paul A.
Stereoselective synthesis of an advanced <i>trans</i>-decalin intermediate towards the total synthesis of anthracimycin.
Chemical communications (Cambridge, England), 2024, 60, 5699-5702
7133013 CIFC17 H22 O5P 21 21 217.18006; 12.9367; 17.2317
90; 90; 90
1600.59Jeanmard, Laksamee; Lodovici, Giacomo; George, Ian; Bray, Joshua T. W.; Whitwood, Adrian C.; Thomas, Gavin H.; Fairlamb, Ian J. S.; Unsworth, William P.; Clarke, Paul A.
Stereoselective synthesis of an advanced <i>trans</i>-decalin intermediate towards the total synthesis of anthracimycin.
Chemical communications (Cambridge, England), 2024, 60, 5699-5702
7133014 CIFC94 H150 Mg N4 Ni2 O8P -110.3314; 12.155; 20.115
85.509; 76.039; 68.417
2279.4Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133015 CIFC67 H100 Mg N4 Ni O4P -111.7869; 13.1585; 21.6061
95.572; 101.159; 101.843
3184.9Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133016 CIFC86 H133 Ca N5 Ni2 O12P -113.1189; 18.636; 19.149
81.507; 86.676; 74.077
4451.9Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133017 CIFC96 H158 Mg N4 Ni2 O8P 1 21/c 128.041; 14.697; 24.348
90; 104.01; 90
9736Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133018 CIFC92 H150 Ca N4 Ni2 O12P 1 n 116.7438; 14.268; 20.0197
90; 97.276; 90
4744.2Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133019 CIFC18 H14 Cl N OP 1 21/c 17.8569; 16.8285; 11.212
90; 104.254; 90
1436.81Sachin, ?; Sharma, Tamanna; Chandra, Devesh; Sumit, ?; Sharma, Upendra
Inherent directing group-enabled Co(III)-catalyzed C-H allylation/vinylation of isoquinolones.
Chemical communications (Cambridge, England), 2024, 60, 5626-5629
7133020 CIFC62 H47 Cl3 N6 O10 P2 Ru2P 1 21/c 119.7908; 15.1911; 23.1446
90; 107.604; 90
6632.4Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133021 CIFC24 H12 Br4 N6I 1 2/a 111.9288; 6.8445; 27.4989
90; 90.376; 90
2245.15Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133022 CIFC56 H41 Br3 Cl4 N4 O6 P2 RuP 1 21/c 118.3915; 14.4654; 20.9301
90; 100.804; 90
5469.55Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133023 CIFC58 H49 Cl N4 O6 P2 RuP -115.601; 21.105; 22.1703
110.152; 101.134; 99.661
6502.66Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133024 CIFC40 H46 Cd N0.5 O17.5 S4P 1 21/n 110.722; 39.433; 14.317
90; 97; 90
6008Su, Jian; Han, Xiao; Ke, Si-Wen; Zhou, Xiao-Cheng; Yuan, Shuai; Ding, Mengning; Zuo, Jing-Lin
Construction of a stable radical hydrogen-bonded metal-organic framework with functionalized tetrathiafulvalene linkers.
Chemical communications (Cambridge, England), 2024, 60, 5812-5815
7133025 CIFC43 H59 B N4 SiP -19.474; 13.9943; 16.2737
90.635; 90.829; 106.097
2072.54Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133026 CIFC57 H67 B N4 O2 SiP 1 21/n 112.9587; 24.1745; 16.8361
90; 103.559; 90
5127.2Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133027 CIFC69 H75 B N4 O2 SiC 1 c 111.765; 23.8074; 23.7692
90; 97.721; 90
6597.3Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133028 CIFC43 H59 B Ge N4P -19.5039; 14.0108; 16.3294
90.542; 90.684; 106.025
2089.55Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133029 CIFC86 H118 B2 N8 O2 Si2P 1 21/n 113.5861; 20.8352; 14.9701
90; 100.035; 90
4172.7Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133030 CIFC48 H59 B F5 N5 SiP 1 21/c 119.2831; 10.4515; 24.172
90; 103.424; 90
4738.5Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133031 CIFCs6 Na3 Nd O54 W10P -111.3552; 15.4905; 16.9027
101.371; 104.424; 91.701
2813.17Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W<sub>5</sub>O<sub>18</sub>)<sub>2</sub>]<sup>9</sup>.
Chemical communications (Cambridge, England), 2024, 60, 5999-6002
7133032 CIFCm Cs8 Na O50 W10P -111.46121; 14.46007; 17.5536
101.11; 99.4298; 103.293
2711.36Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W<sub>5</sub>O<sub>18</sub>)<sub>2</sub>]<sup>9</sup>.
Chemical communications (Cambridge, England), 2024, 60, 5999-6002
7133033 CIFC33 H26 N4 O6P 1 21/c 112.5972; 10.0613; 21.8687
90; 90.553; 90
2771.6Zhu, Shugao; Huang, Wenliang; Liu, Shihan; Yu, Rongjing; Ma, Yufeng; Wang, Hong; Zhang, Rui; Liu, Bin; Lan, Yu; Shen, Ruwei
Synthesis of benzooxepane-fused cyclobutene derivatives <i>via</i> Pd-catalyzed cascade reactions of haloarenes and diynylic ethers.
Chemical communications (Cambridge, England), 2024, 60, 5707-5710
7133034 CIFC42 H68 O8P 1 21 16.1621; 11.6465; 13.7206
90; 102.517; 90
961.28Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133035 CIFC21 H34 O4P 21 21 216.9015; 11.1195; 24.8315
90; 90; 90
1905.6Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133036 CIFC21 H34 O4I 1 2 120.0209; 6.9482; 29.3036
90; 107.026; 90
3897.74Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133037 CIFC23 H28 F3 N O8 SP 1 21 112.4612; 10.5196; 20.4828
90; 107.749; 90
2557.22Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133038 CIFC23 H28 F3 N O8 SP 1 21 111.0308; 11.6724; 11.0847
90; 116.773; 90
1274.22Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133039 CIFC19 H23 N O3P 1 21 110.163; 13.6943; 11.4184
90; 92.889; 90
1587.14Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133040 CIFC19 H24 O2 SP 1 21/n 111.562; 5.6279; 26.4527
90; 92.458; 90
1719.7Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133041 CIFC16 H24 O2P c a 2110.399; 13.561; 9.888
90; 90; 90
1394.4Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133042 CIFC17 H18 O2P 1 21/c 111.0571; 10.1834; 11.8525
90; 102.1; 90
1304.93Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133043 CIFC12 H14 O4P 1 21/n 15.8827; 24.9167; 8.1339
90; 110.149; 90
1119.28Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133044 CIFC18 H18 O4P 1 21/n 15.845; 17.181; 7.9441
90; 107.273; 90
761.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133045 CIFC15 H16 O4P 1 21/c 110.828; 7.9485; 15.2171
90; 95.439; 90
1303.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133046 CIFC17 H18 O5P -15.8137; 8.5017; 16.6639
99.886; 92.872; 108.302
765.58Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133047 CIFC35 H15 B F15 N OP 1 21/n 110.78652; 21.7974; 17.9089
90; 105.265; 90
4062.15Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133048 CIFC29 H8 B F15 N2I 1 2/a 113.6313; 19.4305; 24.194
90; 99.003; 90
6329.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133049 CIFC35 H12 B F15 N4 O2P 1 21/c 112.0468; 16.3233; 15.715
90; 95.2169; 90
3077.45Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133050 CIFC30 H11 B Cl3 F15 N2C 1 2/c 134.981; 9.9268; 19.229
90; 109.205; 90
6305.7Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133051 CIFC27 H7 B F15 NP -111.505; 12.536; 17.074
77.759; 87.576; 77.117
2345.9Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133052 CIFC33 H11 B F15 NP -19.3635; 12.334; 13.652
108.894; 103.287; 96.811
1419.5Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133053 CIFC33 H11 B F15 NP -110.152; 10.204; 14.905
100.952; 99.276; 103.819
1437.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133054 CIFC38 H21 B F15 N3P 1 21/c 112.1553; 18.4902; 15.9842
90; 111.521; 90
3342.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133055 CIFC58.06 H70.12 Cl4.12 F4 I2 N6 O9 SeI 1 2/a 121.6338; 28.0204; 21.9354
90; 98.596; 90
13147.6Liu, Chuan-Zhi; Zhang, Chi; Li, Zhong-Yi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kun; Yan, Meng; Zhai, Bin
Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding.
Chemical communications (Cambridge, England), 2024, 60, 6063-6066
7133056 CIFC32 H34 F3 I N4 O5 SeP -19.5768; 10.0412; 18.3416
96.6; 101.321; 98.752
1690.13Liu, Chuan-Zhi; Zhang, Chi; Li, Zhong-Yi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kun; Yan, Meng; Zhai, Bin
Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding.
Chemical communications (Cambridge, England), 2024, 60, 6063-6066
7133057 CIFC56 H46 Cd2 N6 O10P 21 21 219.6443; 17.67; 36.653
90; 90; 90
6246.2Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133058 CIFC55 H42 Cd2 N6 O10P 21 21 219.6554; 17.7129; 36.6589
90; 90; 90
6269.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133059 CIFC45 H39 N4 O13 Zn4P 21 21 2113.6565; 29.6834; 14.1762
90; 90; 90
5746.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133060 CIFC45 H34 N4 O13 Zn4P 21 21 2113.6827; 14.1989; 29.77
90; 90; 90
5783.7Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133061 CIFC4 H6 Na O14 Re U2C 1 2/m 115.2417; 8.1267; 15.0583
90; 113.798; 90
1706.6Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133062 CIFC8 H12 Na2 O30 Tc2 U4C 1 2/m 115.2356; 8.1216; 15.0053
90; 114.061; 90
1695.39Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133063 CIFC4 H18 O32 Re2 U5P -17.7354; 8.4717; 12.782
94.029; 99.086; 109.92
770.66Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133064 CIFC4 H6 O32 Tc2 U5P -17.7451; 8.4501; 12.7565
93.982; 99.211; 109.708
768.96Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133065 CIFC8 H20 O25.75 Tc U4P b c n14.371; 13.8231; 14.8033
90; 90; 90
2940.7Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133066 CIFC13 H8 Br N SP 1 21/c 111.7154; 14.3463; 7.0036
90; 102.82; 90
1147.77Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of <i>N</i>-β-brominated alkenyl isothiocyanates <i>via</i> dehydrogenation of alkyl isothiocyanates.
Chemical communications (Cambridge, England), 2024, 60, 6015-6018
7133067 CIFC15 H10 Br N SP b c a7.4897; 18.6819; 19.2474
90; 90; 90
2693.13Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of <i>N</i>-β-brominated alkenyl isothiocyanates <i>via</i> dehydrogenation of alkyl isothiocyanates.
Chemical communications (Cambridge, England), 2024, 60, 6015-6018
7133068 CIFC36 H44 N4 O13 S3P 1 21 117.0638; 4.9924; 23.7104
90; 101.092; 90
1982.14Zhao, Chenyang; Li, Zujian; Ji, Lukang; Wang, Hanxiao; Ouyang, Guanghui; Liu, Minghua
Aggregate-state-dependent photochromism and circularly polarized luminescence of a chiral biquinoline amphiphile.
Chemical communications (Cambridge, England), 2024, 60, 6047-6050
7133069 CIFC26 H32 Br2.31 I1.69 N6 O2 ZnP -18.6011; 12.1473; 17.1881
71.236; 80.474; 79.466
1660.7Manna, Subarna; Sahoo, Sangita; Rit, Arnab
Synthesis of quinazolinone scaffolds <i>via</i> a zinc(II)-stabilized amidyl radical-promoted deaminative approach.
Chemical communications (Cambridge, England), 2024, 60, 7097-7100
7133070 CIFC107 H97 Cl3 O4P -110.8817; 15.6992; 25.2074
92.731; 92.591; 108.886
4061.44Hirano, Junichiro; Miyoshi, Sayaka; Yashima, Eiji; Ikai, Tomoyuki; Shinokubo, Hiroshi; Fukui, Norihito
Synthesis of sterically congested double helicene by alkyne cycloisomerization.
Chemical communications (Cambridge, England), 2024, 60, 6035-6038
7133071 CIFC11 H17 N O S2P 1 21/c 115.8974; 7.835; 9.4791
90; 100.682; 90
1160.2Cheng, Yuhe; Hyodo, Tadashi; Yamaguchi, Kentaro; Ohwada, Tomohiko; Otani, Yuko
Complete amide <i>cis</i>-<i>trans</i> switching synchronized with disulfide bond formation and cleavage in a proline-mimicking system.
Chemical communications (Cambridge, England), 2024, 60, 6158-6161
7133072 CIFC19 H20 N2 O4P -18.1324; 11.0134; 20.24
77.534; 79.396; 80.934
1726.67Liu, Zi; Greaney, Michael F.
Aminoarylation of alkynes using diarylanilines.
Chemical communications (Cambridge, England), 2024, 60, 6296-6299
7133073 CIFC15 H11 N SP -19.2993; 9.8997; 13.2708
82.308; 83.479; 77.987
1179.57George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133074 CIFC15 H11 N SP -19.2758; 9.9051; 13.2567
82.254; 83.462; 77.957
1175.69George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133075 CIFC15 H11 N SP -19.2177; 9.9216; 13.2043
82.062; 83.369; 77.928
1164.89George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133076 CIFC15 H11 N SP -19.1868; 9.9277; 13.1688
81.952; 83.305; 77.93
1158.19George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133077 CIFC15 H11 N SP -19.2356; 9.9171; 13.2232
82.118; 83.407; 77.923
1168.48George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133078 CIFC14 H11 N O S2P -19.6697; 10.5598; 13.8151
93.577; 100.035; 113.048
1264.85Wakabayashi, Ryota; Wang, Shuo; Kurogi, Takashi; Yorimitsu, Hideki
Arylation of benzazoles at the 4 positions by activation of their 2-methylsulfinyl groups.
Chemical communications (Cambridge, England), 2024, 60, 6166-6169
7133079 CIFC21 H16 N4 O5 Ru SP b c a10.1221; 16.1027; 25.1176
90; 90; 90
4094Yang, Jing; Zhan, Shaoqi; Wang, Linqin; Yang, Hao; Duan, Lele; Fan, Xiaolei; Liu, Tianqi; Sun, Licheng
Adaptive water oxidation catalysis on a carboxylate-sulfonate ligand with low onset potential.
Chemical communications (Cambridge, England), 2024, 60, 6162-6165
7133080 CIFC54 H58 B2 N6 O2 S2P 1 21/c 120.704; 6.2953; 18.9378
90; 108.615; 90
2339.2Fukami, Shuhei; Mori, Shigeki; Harada, Takunori; Shimizu, Soji
Far-red fluorescence and chiroptical properties of pyrrolopyrrole aza-BODIPYs induced by the <i>B</i>,<i>O</i>-chelation.
Chemical communications (Cambridge, England), 2024, 60, 6170-6173
7133081 CIFC38 H46 B2 F4 N6 S4P -17.7011; 11.6851; 11.8911
75.307; 71.596; 76.096
967.05Fukami, Shuhei; Mori, Shigeki; Harada, Takunori; Shimizu, Soji
Far-red fluorescence and chiroptical properties of pyrrolopyrrole aza-BODIPYs induced by the <i>B</i>,<i>O</i>-chelation.
Chemical communications (Cambridge, England), 2024, 60, 6170-6173
7133082 CIFC25 H22 Br N3 OP 1 21/c 15.946; 22.981; 16.1913
90; 96.653; 90
2197.56Fall, Arona; Magdei, Mihaela; Savchuk, Mariia; Oudeyer, Sylvain; Beucher, Hélène; Brière, Jean-François
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.
Chemical communications (Cambridge, England), 2024, 60, 6316-6319
7133083 CIFC26 H25 N3 O2P 1 21/c 116.9362; 10.0156; 27.6433
90; 106.283; 90
4500.94Fall, Arona; Magdei, Mihaela; Savchuk, Mariia; Oudeyer, Sylvain; Beucher, Hélène; Brière, Jean-François
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.
Chemical communications (Cambridge, England), 2024, 60, 6316-6319
7133084 CIFAl B3 Cl Cs O6P -3 c 17.0716; 7.0716; 18.0458
90; 90; 120
781.52Liu, Haoran; Jiao, Jiahao; Tudi, Abudukadi; Liu, Qingyu; Yang, Zhihua; Pan, Shilie; Zhang, Min
CsAlB<sub>3</sub>O<sub>6</sub>Cl: the rational construction of a KBBF-type structure with aligned <sup>2</sup><sub>∞</sub>[AlB<sub>3</sub>O<sub>6</sub>Cl] layers <i>via</i> introducing unprecedented [AlO<sub>3</sub>Cl] tetrahedra.
Chemical communications (Cambridge, England), 2024, 60, 6516-6519
7133085 CIFC6 I3 N PbP n m a7.8521; 11.3081; 15.9901
90; 90; 90
1419.8Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133086 CIFC5 H12 I NI 4/m7.3846; 7.3846; 7.2299
90; 90; 90
394.263Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133087 CIFC5 H12 I3 N PbP 63/m16.745; 16.745; 8.387
90; 90; 120
2036.6Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133088 CIFC5 H12 I3 N PbP 63/m16.4064; 16.4064; 8.3883
90; 90; 120
1955.38Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133089 CIFC84 H62 N2 O12 S8C 1 c 127.458; 23.377; 11.615
90; 90.454; 90
7455Du, Zhenglin; Xie, Jialin; Liu, Yandie; Tang, Yisong; Chen, Qing; Li, Xia; Zhu, Kelong
A π-extended molecular belt with selective binding capability for fullerene C<sub>70</sub>.
Chemical communications (Cambridge, England), 2024, 60, 6387-6390
7133090 CIFC142 H52 O8 S8P 1 21/n 117.1449; 33.6954; 21.4769
90; 92.559; 90
12394.9Du, Zhenglin; Xie, Jialin; Liu, Yandie; Tang, Yisong; Chen, Qing; Li, Xia; Zhu, Kelong
A π-extended molecular belt with selective binding capability for fullerene C<sub>70</sub>.
Chemical communications (Cambridge, England), 2024, 60, 6387-6390
7133091 CIFC30 H32 N2 O6P -110.405; 10.991; 12.216
109.33; 91.872; 104.146
1268.4Songsermsawad, Sarita; Shemchuk, Oleksii; Robeyns, Koen; Collard, Laurent; E Flood, Adrian; Leyssens, Tom
Simultaneously resolving BINOL and proline using a stoichiometric cocrystal switch.
Chemical communications (Cambridge, England), 2024, 60, 6607-6610
7133092 CIFC45 H37 N O6P 21 21 219.12901; 13.7793; 27.6456
90; 90; 90
3477.58Songsermsawad, Sarita; Shemchuk, Oleksii; Robeyns, Koen; Collard, Laurent; E Flood, Adrian; Leyssens, Tom
Simultaneously resolving BINOL and proline using a stoichiometric cocrystal switch.
Chemical communications (Cambridge, England), 2024, 60, 6607-6610
7133093 CIFC10 H20 Cu2 N5I b a m14.9083; 8.1008; 12.162
90; 90; 90
1468.79Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133094 CIFC10 H20 Cu2 N5I b a m14.8851; 8.1225; 12.2203
90; 90; 90
1477.49Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133095 CIFC10 H20 Cu2 N5I b a m14.7778; 8.2376; 12.5337
90; 90; 90
1525.77Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133096 CIFC10 H20 Cu2 N5I b a m14.8065; 8.2051; 12.4448
90; 90; 90
1511.9Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133097 CIFC10 H20 Cu2 N5I b a m14.8624; 8.1463; 12.2872
90; 90; 90
1487.66Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133098 CIFC10 H20 Cu2 N5I b a m14.8279; 8.1752; 12.366
90; 90; 90
1499.02Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133099 CIFC10 H20 Cu2 N5I b a m14.7531; 8.2731; 12.6466
90; 90; 90
1543.57Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133100 CIFC27 H17 N O3P b c a7.3843; 20.0427; 24.5666
90; 90; 90
3635.89Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133101 CIFC28 H16 F3 N O3P -110.994; 11.0404; 17.6631
83.512; 80.77; 72.972
2018.43Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133102 CIFC32 H19 N O3P b c a7.75825; 18.8157; 31.7145
90; 90; 90
4629.58Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133103 CIFC44 H32 Fe N10P -19.8316; 10.568; 17.2201
81.653; 83.058; 85.688
1754.2Sung, Yu-Shien; Tomat, Elisa
Quinoline-based tetrazolium prochelators: formazan release, iron sequestration, and antiproliferative efficacy in cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 6150-6153
7133104 CIFC26 H25 N O5P 21 21 215.0705; 19.7168; 21.861
90; 90; 90
2185.53Yang, Yang; Yang, Chenchen; Zhu, Xuefeng; Zhang, Li; Liu, Minghua
Interfacial self-assembly of a chiral pyrene exciplex into a superhelix with enhanced circularly polarized luminescence.
Chemical communications (Cambridge, England), 2024, 60, 6631-6634
7133105 CIFC68 H58 Cu2 N6 O16C 1 2/c 132.307; 14.1238; 16.6531
90; 97.426; 90
7535Saura-Sanmartin, Adrian; Cutillas-Font, Guillermo; Martinez-Cuezva, Alberto; Alajarin, Mateo; Esteban-Betegón, Fátima; Pena-Sánchez, Pilar; Gándara, Felipe; Berna, Jose
Mechanical bonding of rigid MORFs using a tetratopic rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 6431-6434
7133106 CIFC68 H60 Co2 N6 O19P n m a16.795; 33.97; 13.8988
90; 90; 90
7929.6Saura-Sanmartin, Adrian; Cutillas-Font, Guillermo; Martinez-Cuezva, Alberto; Alajarin, Mateo; Esteban-Betegón, Fátima; Pena-Sánchez, Pilar; Gándara, Felipe; Berna, Jose
Mechanical bonding of rigid MORFs using a tetratopic rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 6431-6434
7133107 CIFC33 H25 N OP -15.82; 9.093; 23.432
79.032; 87.963; 78.447
1192.7Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133108 CIFC35 H27 Cl2 N O2P 1 21/c 112.4215; 27.311; 9.588
90; 112.62; 90
3002.5Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133109 CIFC29 H23 N O3P 1 21/c 111.302; 22.17; 9.91
90; 107.88; 90
2363Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133110 CIFC27 H25 F3 O5 SP n a 2130.2694; 7.47312; 21.66
90; 90; 90
4899.64Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133111 CIFC25 H19 F3 O4 SC 1 c 17.3296; 14.8403; 19.798
90; 99.989; 90
2120.85Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133112 CIFC24 H19 B F4 OP 1 21/n 16.8567; 19.3806; 14.5799
90; 93.309; 90
1934.25Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133113 CIFC26 H19 F6 N O5 S2P -17.7877; 13.5269; 14.2246
115.433; 102.323; 95.02
1294.53Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133114 CIFC26 H19 F6 N O5 S2P -114.2426; 14.5647; 15.1706
117.808; 98.1608; 104.991
2558.64Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133115 CIFC17 H11 F3 N2 O4P -19.7758; 10.513; 11.2193
90.001; 112.552; 105.12
1021.51Wang, Manqing; Xu, Yuanshuang; Hou, Huihang; Zhang, Xinying; Fan, Xuesen
Divergent synthesis of pyrrolizine derivatives through C-H bond functionalization of pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6536-6539
7133116 CIFC17 H15 F3 N2 O3P 1 21/c 110.9356; 17.2071; 9.5578
90; 113.916; 90
1644.07Wang, Manqing; Xu, Yuanshuang; Hou, Huihang; Zhang, Xinying; Fan, Xuesen
Divergent synthesis of pyrrolizine derivatives through C-H bond functionalization of pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6536-6539
7133117 CIFC39 H50 N PP -110.7562; 13.4826; 14.1323
115.435; 107.508; 96.665
1692Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133118 CIFC33 H36 Br NP 1 21/c 110.4197; 14.0561; 18.9616
90; 100.363; 90
2731.82Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133119 CIFC109 H143 La2 N2 O P5P -115.498; 16.566; 22.288
76.309; 70.924; 69.957
5030.1Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133120 CIFC47 H69 K N O2 PP 1 21/n 111.463; 16.2623; 24.992
90; 97.374; 90
4620.3Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133121 CIFC164 H216 Cl10 K2 La4 N4 O2 P4P -112.833; 16.681; 21.1112
98.117; 100.137; 108.631
4120Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133122 CIFC85.6 H117 Cl La N2 O1.9 P2P 1 21/c 120.5986; 24.7411; 32.569
90; 95.767; 90
16514.2Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133123 CIFC11 H11 N9 OP 1 21/c 16.4786; 15.6097; 13.6164
90; 100.478; 90
1354.05Liu, Ziwei; Jiang, Clancy Zhijian; Bond, Andrew D.; Tosca, Nicholas J.; Sutherland, John D.
Manganese(II) promotes prebiotically plausible non-enzymatic RNA ligation reactions.
Chemical communications (Cambridge, England), 2024, 60, 6528-6531
7133124 CIFC46 H48 Br2 N2 O6 S4P -113.3806; 13.864; 15.8118
114.886; 90.41; 117.953
2272.67Li, Jia; Li, Liang; Mao, Mingming; Li, Rui-Peng; Huo, Xing; Tang, Shouchu
Site-selective synthesis of indanyl-substituted indole derivatives <i>via</i> 1,3-dithiane induced Nazarov cyclization.
Chemical communications (Cambridge, England), 2024, 60, 6540-6543
7133125 CIFC165 H129 Ce4 N39 O27P -122.747; 25.744; 26.168
82.095; 83.235; 63.886
13601Zhao, Lehua; Zhang, Yu; Wang, Huali; Wang, Jing; He, Cheng; Zhao, Liang; Duan, Chunying
Isolation of a copper photocatalyst on a metal-organic cage for the sulfonylation of aryl halides resulting from visible-light-mediated C(sp<sup>2</sup>)-S cross-coupling.
Chemical communications (Cambridge, England), 2024, 60, 6805-6808
7133126 CIFC27 H23 F Ge OP -19.8789; 11.0575; 11.8202
106.201; 104.242; 105.035
1124.69Lu, Xiao-Yu; Qian, Yu-Jun; Sun, Hai-Lun; Su, Meng-Xue; Wang, Zi-Zhen; Jiang, Fan; Zhou, Xin-Yue; Sun, Yan-Xi; Shi, Wan-Li; Wan, Ji-Ru
Photoinduced decarboxylative germylation of α-fluoroacrylic acids: access to germylated monofluoroalkenes.
Chemical communications (Cambridge, England), 2024, 60, 6556-6559
7133127 CIFC14 H16 N4 O5P 1 21/n 113.8775; 7.5913; 15.0147
90; 116.937; 90
1410.2Al Rahal, Okba; Ferguson, Michael; Lennox, Cameron B.; Male, Louise; Friščić, Tomislav
Structure of the caffeine-pyrogallol complex: revisiting a pioneering structural analysis of a model pharmaceutical cocrystal.
Chemical communications (Cambridge, England), 2024, 60, 7431-7434
7133128 CIFC14 H24 N4 O9P 42/n :223.1123; 23.1123; 6.8449
90; 90; 90
3656.4Al Rahal, Okba; Ferguson, Michael; Lennox, Cameron B.; Male, Louise; Friščić, Tomislav
Structure of the caffeine-pyrogallol complex: revisiting a pioneering structural analysis of a model pharmaceutical cocrystal.
Chemical communications (Cambridge, England), 2024, 60, 7431-7434
7133129 CIFC13 H16 Br2 N4 O3 WP 1 21/n 110.5949; 14.4051; 11.7972
90; 91.105; 90
1800.16Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133130 CIFC11 H12 Br2 Cl3 N3 O3 WP -19.2942; 10.3885; 11.1039
63.402; 75.498; 79.694
925.34Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133131 CIFC22 H30 Br Cl3 N6 O4 W2P 21 21 27.857; 15.9287; 12.3215
90; 90; 90
1542.06Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133132 CIFC15 H21 Br2 N5 O WP 1 21/c 111.3229; 8.0358; 21.4613
90; 95.852; 90
1942.56Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133133 CIFC15 H20 O5P -110.7822; 10.9047; 12.0558
88.037; 83.186; 89.353
1406.6Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133134 CIFC18 H23 F3 O7 SP 21 21 218.8302; 11.4492; 20.293
90; 90; 90
2051.6Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133135 CIFC24 H27 F3 O7 SP -113.4729; 13.6729; 14.874
65.885; 84.653; 77.547
2442Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133136 CIFC20 H30 OP -16.0028; 11.2789; 13.1074
64.982; 80.954; 87.69
793.83Dethe, Dattatraya H.; Sharma, Nitin; Juyal, Sakshi; Singh, Prabhakar; Siddiqui, Salman A.
Enantioselective total synthesis of atisane diterpenoids: (+)-sapinsigin H, (+)-agallochaol C, and (+)-16α, 17-dihydroxy-atisan-3-one.
Chemical communications (Cambridge, England), 2024, 60, 7866-7869
7133137 CIFC61 H92 Cr Li N4 O5P -112.3655; 14.1523; 19.2237
69.523; 76.232; 65.51
2850.94D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133138 CIFC62 H95 Cr Li N4 O5P -111.7699; 16.1506; 17.7227
97.669; 105.27; 108.783
2987.77D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133139 CIFC61 H90 Cr K N4 O8P -111.7863; 14.0237; 19.3145
85.096; 78.035; 75.843
3026.2D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133140 CIFC102 H140 Cr2 K2 N8 O5R -3 :H41.8744; 41.8744; 15.4776
90; 90; 120
23503.4D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133141 CIFC140 H202 Cr2 K2 N8 O17P -112.1161; 19.5547; 29.7051
82.767; 81.408; 78.704
6790.16D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133142 CIFC70 H63 B Cl3 F24 N2 O3 PP -112.6492; 13.6605; 21.8343
81.4; 78.136; 78.97
3600.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133143 CIFC149 H136 B2 F48 N4 O6 P2P -113.6399; 16.8477; 19.2953
115.857; 102.316; 98.273
3754.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133144 CIFC45 H60 Cl7 Ga2 N2 O3 PC 1 c 120.964; 12.2176; 20.1457
90; 93.743; 90
5148.9Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133145 CIFC86 H85 B F24 N5 O3 PP -112.1449; 18.623; 20.405
70.624; 73.911; 75.97
4125.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133146 CIFC91 H88 B F24 N2 O3 PP 1 21/n 113.9705; 31.6393; 19.2626
90; 93.898; 90
8494.7Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133147 CIFC89.36 H97.27 B F24 N2 O3 P SiP -113.1456; 17.6698; 20.0734
95.272; 103.875; 91.26
4502.8Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133148 CIFC79 H74 B F24 N2 O3 PP -113.9743; 16.814; 19.335
115.292; 106.112; 94.371
3845.7Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133149 CIFC79 H64 B F24 N2 O3 PP 1 21/c 112.366; 20.9073; 29.743
90; 97.228; 90
7628.6Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133150 CIFC28 H30 N2 O4C 1 c 114.4111; 20.2712; 10.3678
90; 129.444; 90
2338.94Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters <i>via</i> an internal redox reaction/inverse electron-demand hetero-Diels-Alder reaction sequence.
Chemical communications (Cambridge, England), 2024, 60, 6797-6800
7133151 CIFC29 H32 Cl2 N2 O4P -19.9028; 11.7064; 11.8877
89.667; 74.086; 77.512
1291.8Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters <i>via</i> an internal redox reaction/inverse electron-demand hetero-Diels-Alder reaction sequence.
Chemical communications (Cambridge, England), 2024, 60, 6797-6800
7133152 CIFC31 H46 F N S Si2P 1 21 18.1462; 13.1951; 15.8775
90; 96.946; 90
1694.15Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C-H alkynylation of 2-arylthiazoles switched by Ru<sup>II</sup> and Pd<sup>II</sup> catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6679-6682
7133153 CIFC22 H29 N O S SiP -18.798; 12.4654; 21.0908
104.49; 90.974; 91.921
2237.4Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C-H alkynylation of 2-arylthiazoles switched by Ru<sup>II</sup> and Pd<sup>II</sup> catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6679-6682
7133154 CIFC38 H39 N O8P 21 21 217.7775; 19.6476; 22.0751
90; 90; 90
3373.28Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-Ichi
Total synthesis of 1,4a-di-<i>epi-ent</i>-pancratistatin, exemplifying a stereodivergent approach to pancratistatin isomers.
Chemical communications (Cambridge, England), 2024, 60, 6757-6760
7133155 CIFC51 H39 Cl2 N O13P 1 21 110.8258; 13.1828; 15.3126
90; 79.363; 90
2147.78Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-Ichi
Total synthesis of 1,4a-di-<i>epi-ent</i>-pancratistatin, exemplifying a stereodivergent approach to pancratistatin isomers.
Chemical communications (Cambridge, England), 2024, 60, 6757-6760
7133156 CIFC6 H22 Br5 In N2 O2P n m a20.264; 7.9353; 11.0226
90; 90; 90
1772.4Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and soft crystal structure-induced broad emission of (NH<sub>3</sub>C<sub>6</sub>H<sub>12</sub>NH<sub>3</sub>)InBr<sub>5</sub>·2H<sub>2</sub>O.
Chemical communications (Cambridge, England), 2024, 60, 7757-7760
7133157 CIFC6 H22 Br5 In N2 O2P 1 21/n 17.8333; 20.223; 10.9317
90; 91.232; 90
1731.3Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and soft crystal structure-induced broad emission of (NH<sub>3</sub>C<sub>6</sub>H<sub>12</sub>NH<sub>3</sub>)InBr<sub>5</sub>·2H<sub>2</sub>O.
Chemical communications (Cambridge, England), 2024, 60, 7757-7760
7133158 CIFC18 H14 O2P 1 21/c 111.2312; 14.7726; 8.2671
90; 109.062; 90
1296.42Zhang, Xu; Chang, Mengfan; Xu, Xuefeng; Zhao, Qiang
Direct access to furan and cyclopropane derivatives <i>via</i> palladium-catalyzed C-H activation/alkene insertion/annulation.
Chemical communications (Cambridge, England), 2024, 60, 6769-6772
7133159 CIFC19 H19 N O4 SP 1 21/c 18.301; 11.0651; 18.7113
90; 93.468; 90
1715.51Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133160 CIFC27 H29 N O4 S2P 1 21/n 19.2418; 19.5215; 14.0366
90; 99.178; 90
2499.98Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133161 CIFC20 H21 N O5 SP -18.0093; 9.9303; 13.0524
92.274; 107.728; 106.033
941.63Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133162 CIFC12 H18 N2 O4C 1 2/c 123.2511; 6.0802; 18.4786
90; 97.79; 90
2588.2Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133163 CIFC18 H22 N2 O4P -19.5021; 9.6751; 10.0293
77.914; 71.586; 89.936
853.33Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133164 CIFC22 H29 N3 O5P -19.6012; 10.4718; 11.4984
86.861; 70.637; 79.609
1072.78Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133165 CIFC19 H22 N O4P 1 21/c 115.1005; 9.909; 11.5159
90; 93.934; 90
1719.1Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133166 CIFC32 H52 Bi2 F12 N4 Sb2C 1 2/c 136.971; 11.0199; 21.471
90; 101.205; 90
8581Sen, Nilanjana; Sarkar, Pallavi; Meena, Yadram; Tothadi, Srinu; Pati, Swapan K.; Khan, Shabana
Synthesis and catalytic application of a donor-free bismuthenium cation.
Chemical communications (Cambridge, England), 2024, 60, 6877-6880
7133167 CIFC93 H88 Ce4 N4P 1 21/c 18.0983; 17.5589; 27.1102
90; 90.172; 90
3854.98Gupta, Himanshu; Vincenzini, Brett D.; Bacon, Alexandra M.; Schelter, Eric J.
Assembly of a trapped valent Ce<sup>III/IV</sup>-TCNQ complex through metal-ligand redox cooperativity.
Chemical communications (Cambridge, England), 2024, 60, 6909-6912
7133168 CIFC7 H6 O2P 1 21/n 15.502; 5.137; 21.927
90; 97.045; 90
615.1Sun, Hainan; Li, Lili; Chen, Yahui; Kim, Yong Beom; Kim, Hyunseung; Fei, Liangshuang; Shao, Zongping; Jung, WooChul
Crystal structure optimization of copper oxides for the benzyl alcohol oxidation reaction.
Chemical communications (Cambridge, England), 2024, 60, 7224-7227
7133169 CIFC54 H53 N3P -110.502; 11.537; 19.141
96.877; 98.17; 99.193
2241.9Naniyil, Athira; Koroth Valappil, Naveen; Andrews, Alex P.; Gokulnath, Sabapathi
Carbazole-embedded <i>p</i>-benziporphyrinoid: synthesis, structure and a reversible chemodosimeter for mercury(II) ions.
Chemical communications (Cambridge, England), 2024, 60, 6957-6960
7133170 CIFC56 H54 Cl7 Hg N3R -3 :H43.456; 43.456; 14.847
90; 90; 120
24281Naniyil, Athira; Koroth Valappil, Naveen; Andrews, Alex P.; Gokulnath, Sabapathi
Carbazole-embedded <i>p</i>-benziporphyrinoid: synthesis, structure and a reversible chemodosimeter for mercury(II) ions.
Chemical communications (Cambridge, England), 2024, 60, 6957-6960
7133171 CIFC38 H53 Au N4 SiP -113.0228; 16.875; 18.996
76.362; 79.196; 70.713
3801.7Bakhoda, Abolghasem 'Gus'
Gold(I)-catalyzed homologation of aryl aldehydes with trimethylsilyldiazomethane.
Chemical communications (Cambridge, England), 2024, 60, 6937-6940
7133172 CIFC116.94 H127.44 Cl8.84 N12P -114.354; 18.2341; 23.2636
110.586; 101.322; 93.081
5538.9Heim, Gavin P.; Hirahara, Masanari; Dev, Vidhya M.; Agapie, Theodor
Synthesis and electronic properties of nitrogen-rich nanographene.
Chemical communications (Cambridge, England), 2024, 60, 7343-7346
7133173 CIFC25 H47 Ir P2P b c a10.0014; 17.1635; 28.5541
90; 90; 90
4901.6Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133174 CIFC25 H47 Ir P2P 1 21/c 110.405; 18.494; 13.748
90; 109.51; 90
2494Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133175 CIFC25 H49 Ir P2P b c a17.8681; 14.8775; 38.003
90; 90; 90
10102.4Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133176 CIFC5 H8 Cl F2 NP n m a10.0074; 7.0673; 9.5009
90; 90; 90
671.95Charlesworth, Natalie G.; Arunprasath, Dhanarajan; Graham, Mark A.; Argent, Stephen P.; Datsenko, Oleksandr P.; Mykhailiuk, Pavel K.; Denton, Ross M.
Modular synthesis of cyclic β-difluoroamines.
Chemical communications (Cambridge, England), 2024, 60, 7701-7704
7133177 CIFC29 H28 N0 O4C 1 2/c 119.9766; 15.8235; 15.6346
90; 93.935; 90
4930.4Ren, Yue; Shi, Wangyu; Tang, Yi; Guo, Hongchao
Phosphine-catalyzed (3+3) annulation of cinnamaldehyde-derived Morita-Baylis-Hillman carbonates with dinucleophiles.
Chemical communications (Cambridge, England), 2024, 60, 6897-6900
7133178 CIFC23 H18 N2 O5P 1 21/c 111.6492; 7.4491; 22.0277
90; 97.248; 90
1896.2He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-catalyzed dearomative [3+2] cycloaddition of 4-nitroisoxazoles with allenoates or Morita-Baylis-Hillman carbonates.
Chemical communications (Cambridge, England), 2024, 60, 6961-6964
7133179 CIFC15 H12 N4 O5 SP 1 21/c 113.0981; 11.5834; 10.0872
90; 100.284; 90
1505.85He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-catalyzed dearomative [3+2] cycloaddition of 4-nitroisoxazoles with allenoates or Morita-Baylis-Hillman carbonates.
Chemical communications (Cambridge, England), 2024, 60, 6961-6964
7133180 CIFC37 H39 B O2 SiC 1 2/c 116.206; 14.988; 26.246
90; 99.955; 90
6279Fujii, Ikuya; Hirata, Haruka; Moniwa, Hirokazu; Shintani, Ryo
Synthesis of (1-silyl)allylboronates by KO<i>t</i>Bu-catalyzed ring-opening <i>gem</i>-silylborylation of cyclopropenes.
Chemical communications (Cambridge, England), 2024, 60, 6921-6924
7133181 CIFC29 H46 Cr O2 P2P -110.4305; 10.4775; 14.5388
78.486; 83.946; 71.492
1474.9Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133182 CIFC29 H46 Cr O2 P2P 1 21 18.2502; 15.8605; 11.8231
90; 106.188; 90
1485.74Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133183 CIFC46 H83 Cr2 N2 O4.5 P4P 1 21/n 115.7583; 14.4111; 24.856
90; 107.974; 90
5369.2Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133184 CIFC26 H21 N O4P 1 21 16.9055; 21.4299; 27.6189
90; 92.031; 90
4084.6Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133185 CIFC24 H21 Cl N2 O3P -19.6896; 10.1998; 10.8323
89.99; 71.675; 84.875
1011.78Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133186 CIFC34 H30 N2 O3P 1 21/c 111.847; 18.1061; 13.0266
90; 95.964; 90
2779.1Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133187 CIFC10 H11 N O3P 1 21/c 19.9227; 5.672; 16.1656
90; 99.498; 90
897.35Winter, Johannes; Lühr, Susan; Hochadel, Kyra; Gálvez-Vázquez, María de Jesús; Prenzel, Tobias; Schollmeyer, Dieter; Waldvogel, Siegfried R.
Simple electrochemical synthesis of cyclic hydroxamic acids by reduction of nitroarenes.
Chemical communications (Cambridge, England), 2024, 60, 7065-7068
7133188 CIFC81 H106 N2 O18P 1 21/c 112.3241; 33.684; 20.229
90; 96.013; 90
8351Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024, 60, 6889-6892
7133189 CIFC93 H110 N6 O14P -112.08; 12.4509; 29.1324
94.272; 92.465; 106.74
4174.8Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024, 60, 6889-6892
7133190 CIFC52 H76 Fe N2 O2P -19.5346; 13.1604; 18.8315
91.84; 90.463; 91.367
2361Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133191 CIFC37 H28 O8P 1 21/c 110.323; 19.0774; 8.7024
90; 114.576; 90
1558.56Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133192 CIFC5 H6 O4P -15.006; 7.2628; 8.6451
106.71; 102.405; 92.116
292.37Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133193 CIFC26.9 H40.71 Cl6.1 Ga2 N4 O P PtP -18.30726; 15.0654; 15.9963
70.9877; 84.8936; 79.8892
1862.28Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133194 CIFC27 H41 Cl6 In2 N4 O P PtP 1 21/n 18.88651; 12.2296; 35.1991
90; 93.5845; 90
3817.9Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133195 CIFC28.77 H41.3 Cl6.23 In2 N4 O P PtP -18.71612; 14.4778; 17.6581
65.9038; 81.2608; 73.8299
1951.78Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133196 CIFC28 H22 N O2 PP -19.2305; 9.3886; 15.0613
83.016; 81.79; 62.191
1140.4Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133197 CIFC29 H24 N O3 PP -110.1021; 10.6285; 12.0861
95.272; 112.661; 92.657
1187.71Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133198 CIFC29.6 H25.2 Cl1.2 N O3 PP -19.9338; 11.4115; 13.4261
91.104; 99.247; 107.898
1425.68Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133199 CIFC46 H41 N2 O8 S2P -110.581; 10.781; 20.524
88.303; 85.635; 63.604
2091.1Bhati, Kuldeep Singh; Sharma, Siddharth
Electrochemically-driven difunctionalization of the isocyanide and Mumm rearrangement cascade: expeditious synthesis of <i>N</i>-acyl-<i>N</i>-alkyl <i>S</i>-thiocarbamates.
Chemical communications (Cambridge, England), 2024, 60, 7355-7358
7133200 CIFC26 H19 Cl F6 N2 O4P b c n16.652; 14.997; 21.13
90; 90; 90
5276.8Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
<i>N</i>-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction <i>via</i> α-C(sp<sup>3</sup>)-H activation strategy.
Chemical communications (Cambridge, England), 2024, 60, 7180-7183
7133201 CIFC15 H13 N O2C 1 2/c 112.719; 13.852; 14.156
90; 97.096; 90
2475Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
<i>N</i>-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction <i>via</i> α-C(sp<sup>3</sup>)-H activation strategy.
Chemical communications (Cambridge, England), 2024, 60, 7180-7183
7133202 CIFC38 H28 O3 P2P b c a16.51047; 16.41081; 23.08005
90; 90; 90
6253.54Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133203 CIFC19 H13 P SC 1 2/c 114.248; 13.5359; 15.8127
90; 90.772; 90
3049.35Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133204 CIFC24 H22 N O PP n a 2117.3159; 9.40206; 12.4887
90; 90; 90
2033.22Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133205 CIFC19 H13 P SeC 1 2/c 114.1963; 13.7375; 15.8281
90; 90.897; 90
3086.4Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133206 CIFC26 H20 N O2 P SP 1 21/c 18.19512; 13.942; 19.4641
90; 99.7093; 90
2192.04Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133207 CIFC34 H36 N O2 P SP 21 21 219.31097; 12.97197; 24.0692
90; 90; 90
2907.12Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133208 CIFC44 H33 B F4 N PP c a 2112.867; 13.069; 21.505
90; 90; 90
3616.3Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133209 CIFC25.5 H19 B Cl F3 N PP 1 21/c 19.5904; 16.0488; 14.2154
90; 101.406; 90
2144.74Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133210 CIFC31 H23 N O3 P2P 1 21/c 111.81181; 19.91502; 11.98573
90; 118.939; 90
2467.38Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133211 CIFC38 H28 O3 P2P b c a16.3712; 16.281; 22.9501
90; 90; 90
6117.11Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133212 CIFC19 H14 O2 PC 1 2/c 120.3958; 13.4454; 12.1945
90; 117.604; 90
2963.44Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133213 CIFC19 H13 P SeC 1 2/c 114.0369; 13.6803; 15.7202
90; 90.789; 90
3018.45Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133214 CIFC19 H13 O PP -17.2774; 8.0944; 13.1388
81.7506; 79.8049; 70.6319
715.63Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133215 CIFC25 H18 N PP 21 21 218.9413; 13.6176; 15.5673
90; 90; 90
1895.46Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133216 CIFC44 H20 B Cl2 F15 N PP -111.2365; 12.2624; 14.8185
83.39; 78.06; 74.601
1921.98Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133217 CIFC31 H30 N PP 1 21/n 19.0484; 18.306; 14.4219
90; 90.4144; 90
2388.78Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133218 CIFC27 H19 F6 N2 O4 P S2P -18.3718; 17.3368; 20.1621
113.925; 91.4063; 93.9353
2664.18Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133219 CIFC19 H13 P SC 1 2/c 114.0811; 13.4388; 15.6879
90; 90.464; 90
2968.57Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133220 CIFC27 H38 N2 O5 S SiP 1 21 18.956; 12.4093; 12.9018
90; 95.349; 90
1427.63Mroczyńska, Karina; Dobrzańska, Liliana; Rafiński, Zbigniew
Enantioselective synthesis of C3-functionalized 2,1-benzothiazine 2,2-dioxides by N-heterocyclic carbene catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7176-7179
7133221 CIFC41 H35 Cl3 N0.5 O5 PP -111.7184; 12.545; 14.696
101.781; 98.985; 114.481
1853.15Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133222 CIFC58 H51.67 N2 O8 P2P b c a21.3419; 21.1766; 21.9827
90; 90; 90
9935.1Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133223 CIFC29 H24 Cl4 F N O2 PP -110.835; 12.7978; 20.779
81.75; 80.192; 89.486
2809.45Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133224 CIFC18 H13 N3 O2P -16.902; 13.8797; 16.3061
66.241; 89.878; 76.826
1385Chatterjee, Sarat; Khatun, Rousunara; Ali, Mahammad; Chowdhury, Chinmay
A solvent controlled regioselective synthesis of 2- and 4-substituted α-carbolines under palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7427-7430
7133225 CIFC19 H16 N2P 1 21/n 113.4739; 7.1393; 14.6043
90; 101.576; 90
1376.27Chatterjee, Sarat; Khatun, Rousunara; Ali, Mahammad; Chowdhury, Chinmay
A solvent controlled regioselective synthesis of 2- and 4-substituted α-carbolines under palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7427-7430
7133226 CIFC56 H92 Mg2 N4 O2 Si4P 1 21/n 115.637; 11.51056; 17.4414
90; 108.662; 90
2974.23O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133227 CIFC42 H68 K Mg N2 O3 Si2P 1 21/n 114.3212; 20.5716; 15.38509
90; 94.3942; 90
4519.28O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133228 CIFC66 H112 K2 Mg2 N4 O6 Si4P -110.9645; 15.9181; 23.3852
70.892; 89.038; 72.072
3653.33O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133229 CIFC138 H224 K4 Mg4 N12 O4 Si8P -116.3939; 21.2191; 21.8811
81.3508; 89.9089; 88.1901
7521.29O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133230 CIFC24 H18 O5P -18.3038; 11.289; 11.546
63.736; 87.201; 78.91
951.7Singh, Sanjay; Sharma, Pragya; Dutta, Sayantan; Vishwakarma, Rahul; Hazra, Chinmoy K.
An organocatalytic domino annulation approach <i>via</i> C(sp<sup>2</sup>)-OMe cleavage to unlock the synthesis of pyranochromenones enabled by HFIP.
Chemical communications (Cambridge, England), 2024, 60, 7200-7203
7133231 CIFC24 H17 Cl O5P -17.3859; 10.8372; 12.379
101.327; 97.246; 92.314
961.6Singh, Sanjay; Sharma, Pragya; Dutta, Sayantan; Vishwakarma, Rahul; Hazra, Chinmoy K.
An organocatalytic domino annulation approach <i>via</i> C(sp<sup>2</sup>)-OMe cleavage to unlock the synthesis of pyranochromenones enabled by HFIP.
Chemical communications (Cambridge, England), 2024, 60, 7200-7203
7133232 CIFC6 H36 Ho2 O30R -3 :H30.5; 30.5; 7.127
90; 90; 120
5742El Alouani Dahmouni, Nadia; Orts-Arroyo, Marta; Sanchis-Perucho, Adrián; Moliner, Nicolás; Mayans, Júlia; Pacheco, Mario; Castro, Isabel; De Munno, Giovanni; Marino, Nadia; Ruiz-García, Rafael; Martínez-Lillo, José
Magnetocaloric efficiency tuning through solvent-triggered 3D to 2D interconversion in holmium(III)-based dynamic MOFs.
Chemical communications (Cambridge, England), 2024, 60, 7451-7454
7133233 CIFC6 H20 Ho2 O22P 1 21/c 110.9347; 9.604; 9.9542
90; 114.143; 90
953.92El Alouani Dahmouni, Nadia; Orts-Arroyo, Marta; Sanchis-Perucho, Adrián; Moliner, Nicolás; Mayans, Júlia; Pacheco, Mario; Castro, Isabel; De Munno, Giovanni; Marino, Nadia; Ruiz-García, Rafael; Martínez-Lillo, José
Magnetocaloric efficiency tuning through solvent-triggered 3D to 2D interconversion in holmium(III)-based dynamic MOFs.
Chemical communications (Cambridge, England), 2024, 60, 7451-7454
7133234 CIFC21 H20 O4P 21 21 218.5423; 12.3659; 16.7686
90; 90; 90
1771.32Zeng, Hongkun; Wen, Gang; Lin, Lili; Feng, Xiaoming
Asymmetric dearomatization of benzyl 1-naphthyl ethers <i>via</i> [1,3] O-to-C rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7507-7510
7133235 CIFC55 H88 B2 Co F8 N4 O7P 1 21 112.6042; 16.7477; 13.9724
90; 90.008; 90
2949.45Zeng, Hongkun; Wen, Gang; Lin, Lili; Feng, Xiaoming
Asymmetric dearomatization of benzyl 1-naphthyl ethers <i>via</i> [1,3] O-to-C rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7507-7510
7133236 CIFC48 H96 Al4 Eu4 N8 O32I 1 2/a 127.7753; 10.2408; 29.891
90; 117.95; 90
7510.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133237 CIFC216 H440 Al16 Er16 N40 O136I 1 2/a 128.9871; 10.1594; 27.5988
90; 99.049; 90
8026.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133238 CIFC48 H96 Al4 N8 O32 Sm4I 1 2/a 127.9072; 10.2096; 29.8833
90; 118.087; 90
7511.7Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133239 CIFC47.99 H95.97 Al4 Gd4 N8 O32I 1 2/a 127.5463; 10.2945; 29.7052
90; 117.751; 90
7454.8Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133240 CIFC51 H103 Al4 Dy4 N9 O33I 1 2/a 129.1901; 10.2991; 27.6382
90; 98.946; 90
8207.8Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133241 CIFC51 H101 Al4 Ho4 N9 O33I 1 2/a 128.9677; 10.1285; 27.67
90; 99.14; 90
8015.3Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133242 CIFC48 H96 Al4 N8 O32 Tm4I 1 2/a 127.599; 10.1083; 28.8433
90; 99.182; 90
7943.6Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133243 CIFC54 H110 Al4 N10 O34 Tb4I 1 2/a 127.9239; 10.1329; 28.9993
90; 99.256; 90
8098.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133244 CIFC106 H92.03 N6 O18P -114.4561; 21.9459; 22.0092
60.305; 83.03; 74.276
5837.8Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133245 CIFC102 H90 N6 O18P -114.3348; 21.7619; 21.9674
114.642; 97.609; 108.079
5642.86Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133246 CIFC107 H98.1 N6 O18P -114.4122; 21.9201; 22.0159
60.357; 83.564; 74.23
5815.3Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133247 CIFC144 H135 N9 O27C 1 2/c 138.116; 21.9306; 42.5599
90; 103.44; 90
34601.8Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133248 CIFC12 H36 Ag Br11.74 Cl0.26 N4 SbP 1 c 18.6321; 7.8942; 25.961
90; 90.123; 90
1769.1Rajput, Shubham Ajaykumar; Antharjanam, Sudhadevi; Chandiran, Aravind Kumar
An above-room-temperature ferroelectric two-dimensional halide double perovskite with direction dependent properties.
Chemical communications (Cambridge, England), 2024, 60, 7898-7901
7133249 CIFC144 H290 Cu48 N16 O189 P16 S20C 1 2 132.3485; 19.7547; 32.5262
90; 112.66; 90
19180.9Teng, Qian; Gao, Ran; Bao, Song-Song; Zheng, Li-Min
Cu<sub>12</sub>-cluster-based metal-organic framework as a metastable intermediate in the formation of a layered copper phosphonate.
Chemical communications (Cambridge, England), 2024, 60, 7765-7768
7133250 CIFC9.5 H19 Cu2 N O10 P SP 21 21 217.0932; 7.3733; 31.2935
90; 90; 90
1636.66Teng, Qian; Gao, Ran; Bao, Song-Song; Zheng, Li-Min
Cu<sub>12</sub>-cluster-based metal-organic framework as a metastable intermediate in the formation of a layered copper phosphonate.
Chemical communications (Cambridge, England), 2024, 60, 7765-7768
7133251 CIFC34 H35 N3 O4 SP 1 21/c 114.791; 11.623; 18.6337
90; 109.354; 90
3022.4Sun, Zetian; Zhang, Jianting; Du, Xiaohua; Liu, Lulu; Gao, Shuo; Qi, Chenchen; Li, Xiaoqing; Xu, Xiangsheng
Photoinduced EnT-mediated sulfonamidylimination of alkenes and (hetero)arenes with iminophenylacetic acid oxime esters.
Chemical communications (Cambridge, England), 2024, 60, 7934-7937
7133252 CIFC61 H68 Cl2 O13R 3 c :H13.5991; 13.5991; 52.4778
90; 90; 120
8404.8Liu, Rui; Li, Ming; Liu, Zhongwen; Hua, Bin
Separation of cyclohexanol from cyclohexanol/cyclohexene mixtures by crystals of pillar[6]arene containing three benzoquinone units.
Chemical communications (Cambridge, England), 2024, 60, 7626-7629
7133253 CIFC39 H45 N3 O12P 1 21/c 116.1387; 28.3321; 8.3321
90; 95.419; 90
3792.8Wu, Simei; Tao, Wei; Wang, Tao; Xu, Jieqiong; Wei, Peifa
A crown ether embedded responsive π-gelator for transition from a one-component gel to a two-component gel.
Chemical communications (Cambridge, England), 2024, 60, 8232-8235
7133254 CIFC37 H41 N2 O12P 1 21/c 131.3061; 4.701; 26.9834
90; 93.029; 90
3965.6Wu, Simei; Tao, Wei; Wang, Tao; Xu, Jieqiong; Wei, Peifa
A crown ether embedded responsive π-gelator for transition from a one-component gel to a two-component gel.
Chemical communications (Cambridge, England), 2024, 60, 8232-8235
7133255 CIFC50 H36 O2P 1 21/n 117.155; 10.5253; 19.426
90; 91.508; 90
3506.4Sheokand, Sonu; Sharma, Sunita; Mohite, Manali A.; Rajaraman, Gopalan; Balakrishna, Maravanji S.
ZnCl<sub>2</sub>-catalysed transfer hydrogenation of carbonyls and chemoselective reduction of the CC bond in α,β-unsaturated ketones.
Chemical communications (Cambridge, England), 2024, 60, 7733-7736
7133256 CIFC48 H36 N2 O6 ZnP 1 21/c 17.9091; 23.3932; 20.4994
90; 90.281; 90
3792.74Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133257 CIFC48 H36 N2 O6 ZnP 1 21/c 17.9164; 23.6249; 20.5918
90; 91.802; 90
3849.3Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133258 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8927; 23.5873; 20.5265
90; 91.988; 90
3819.1Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133259 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8858; 23.506; 20.4093
90; 91.544; 90
3781.8Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133260 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8902; 23.5724; 20.3308
90; 92.206; 90
3778.54Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133261 CIFC144 H212 K2 N2 O26 Ti2P -113.452; 22.8729; 23.7434
101.621; 94.411; 90.086
7133.5Ishida, Yutaka; Nakanishi, Yusuke; Hiratsuka, Takuma; Kawaguchi, Hiroyuki
Hydrazido complexes prepared by methylation of an anionic end-on bridging dinitrogen dititanium complex.
Chemical communications (Cambridge, England), 2024, 60, 7459-7462
7133262 CIFC108 H158 K2 N2 O10 Ti2C 1 c 113.92; 25.4342; 30.2821
90; 103.153; 90
10439.9Ishida, Yutaka; Nakanishi, Yusuke; Hiratsuka, Takuma; Kawaguchi, Hiroyuki
Hydrazido complexes prepared by methylation of an anionic end-on bridging dinitrogen dititanium complex.
Chemical communications (Cambridge, England), 2024, 60, 7459-7462
7133263 CIFC64 H64 N4P 1 21/n 112.6774; 23.2733; 17.2556
90; 92.162; 90
5087.6Jiang, Zhiyan; Kuninobu, Yoichiro
Synthesis of a novel twisted π-conjugated macrocycle <i>via</i> double Friedel-Crafts reaction and its physical properties.
Chemical communications (Cambridge, England), 2024, 60, 7642-7645
7133264 CIFC77 H61 Li8 N7 O19P -19.8956; 13.8451; 14.417
95.736; 94.844; 102.727
1905.5Li, Shu-Fan; Meng, Ya-Ru; Xu, Min-Jie; Zhang, Gen; Su, Jian
Construction of a redox-active metal-organic framework with an octanuclear lithium one-dimensional building block.
Chemical communications (Cambridge, England), 2024, 60, 8047-8050
7133265 CIFC136 H204 Ca4 N8 Zn4P -115.2503; 16.0371; 16.0776
69.051; 69.699; 71.172
3354.3Pearce, Kyle G.; Neale, Samuel E.; McMullin, Claire L.; Mahon, Mary F.; Hill, Michael S.
Pathway to a molecular calcium methyl.
Chemical communications (Cambridge, England), 2024, 60, 7882-7885
7133266 CIFC72 H116 Ca2 N4P 1 21/n 113.5951; 19.1092; 14.1535
90; 108.43; 90
3488.37Pearce, Kyle G.; Neale, Samuel E.; McMullin, Claire L.; Mahon, Mary F.; Hill, Michael S.
Pathway to a molecular calcium methyl.
Chemical communications (Cambridge, England), 2024, 60, 7882-7885
7133267 CIFC48 H31 Cl2 NP -110.6735; 11.3393; 15.9814
96.998; 104.429; 106.09
1761.56Wang, Ru-Jia; Zheng, Fan; Liu, Xiao-Long; Wu, Yu-Lan; Jin, Jia-Ming; Li, Ze-Yan; Chen, Wen-Cheng; Huo, Yanping
A through-space charge transfer pyrene-based fluorophore with anti-quenching behavior for deep-blue organic light-emitting devices.
Chemical communications (Cambridge, England), 2024, 60, 7946-7949
7133268 CIFC20 H18 O4P 21 21 216.3415; 8.4205; 30.8465
90; 90; 90
1647.16Tan, Zheng; Yihuo, Aying; Wu, Zhao; Wang, Fei; Dong, Shunxi; Feng, Xiaoming
Concise synthesis of chiral γ-butenolides <i>via</i> an allylation/lactonization cascade reaction.
Chemical communications (Cambridge, England), 2024, 60, 7926-7929
7133269 CIFC79 H69.5 Cd F12 N8.5 O8 P2P 1 21/n 112.4369; 24.8732; 25.4913
90; 101.228; 90
7734.7Wang, Shih-Yu; Lin, Lin-Ting; Rani, Alisha; Lee, Guan-Sian; Chan, Yi-Tsu
Stepwise construction of a metallocatenane based on non-labile bis(terpyridine)-Cd<sup>II</sup> complexes.
Chemical communications (Cambridge, England), 2024, 60, 7914-7917
7133270 CIFC26 H28 B N3P 1 21/c 18.4111; 15.3474; 17.0335
90; 96.326; 90
2185.4Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133271 CIFC32 H33 B2 N3P -18.9434; 12.002; 13.5298
105.413; 90.951; 109.556
1310.34Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133272 CIFC34 H43 B2 N3P 1 21/n 111.6929; 17.5821; 14.6284
90; 104.319; 90
2914Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133273 CIFC26 H28 B2 F3 N3P c a 2113.4867; 12.7379; 13.3863
90; 90; 90
2299.7Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133274 CIFC32 H33 B2 Cl2 N3P -18.2484; 8.6731; 22.3744
81.768; 85.754; 62.036
1399.1Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133275 CIFC26 H28 B2 Cl3 N3P 1 21/c 115.6649; 11.3864; 15.8645
90; 115.787; 90
2547.9Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133276 CIFC27 H31 B I N3P 1 21/c 18.0398; 28.378; 11.9315
90; 108.797; 90
2577Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133277 CIFC94 H162 Be2 Cl2 Li2 N4 O14 Si4P 1 21/c 121.4089; 22.319; 22.5227
90; 102.668; 90
10499.9Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133278 CIFC48 H86 Be Cl K N2 O9 Si2P 1 21/n 110.5322; 21.8852; 24.244
90; 92.113; 90
5584.43Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133279 CIFC50 H90 Be Cl N2 Na O10 Si2P 1 21/c 115.1421; 20.7692; 18.2654
90; 91.531; 90
5742.2Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133280 CIFC52.5 H86 Be Cl N2 O6 Rb Si2P 1 21/n 116.7051; 21.103; 17.1977
90; 103.361; 90
5898.57Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133281 CIFC58 H94 Be Cl N2 Na O8 Si2P 1 21/n 112.1829; 17.5093; 29.91
90; 96.725; 90
6336.33Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133282 CIFC46 H82 Be Cl K N2 O8 Si2P 1 21 114.9011; 19.7649; 18.0278
90; 93.633; 90
5298.86Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133283 CIFC24 H21 N O6 SP 21 21 219.792; 10.139; 21.399
90; 90; 90
2124.5Yang, Ji Seon; Kim, Sung-Gon
Catalytic enantioselective [3+2] and [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines with γ- or δ-hydroxy-α,β-unsaturated ketones.
Chemical communications (Cambridge, England), 2024, 60, 7954-7957
7133284 CIFC21 H21 N O6 SP 41 21 28.4145; 8.4145; 56.119
90; 90; 90
3973.4Yang, Ji Seon; Kim, Sung-Gon
Catalytic enantioselective [3+2] and [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines with γ- or δ-hydroxy-α,β-unsaturated ketones.
Chemical communications (Cambridge, England), 2024, 60, 7954-7957
7133285 CIFC25 H51 Os TaC 1 2/c 117.7258; 16.513; 19.8168
90; 104.405; 90
5618.14Lachguar, Abdelhak; Ye, Christopher Z.; Kelly, Sheridon N.; Jeanneau, Erwann; Del Rosal, Iker; Maron, Laurent; Veyre, Laurent; Thieuleux, Chloé; Arnold, John; Camp, Clément
CO<sub>2</sub> cleavage by tantalum/M (M = iridium, osmium) heterobimetallic complexes.
Chemical communications (Cambridge, England), 2024, 60, 7878-7881
7133286 CIFC11 H18 O OsP 1 21/n 18.149; 11.0276; 13.2481
90; 101.769; 90
1165.5Lachguar, Abdelhak; Ye, Christopher Z.; Kelly, Sheridon N.; Jeanneau, Erwann; Del Rosal, Iker; Maron, Laurent; Veyre, Laurent; Thieuleux, Chloé; Arnold, John; Camp, Clément
CO<sub>2</sub> cleavage by tantalum/M (M = iridium, osmium) heterobimetallic complexes.
Chemical communications (Cambridge, England), 2024, 60, 7878-7881
7133287 CIFC30 H22 Co N12 O6 S4P -17.7485; 10.1105; 12.1657
103.064; 92.24; 112.226
851.18Shekhawat, Bhawana; Gahlaut, Puneet Singh; Gautam, Deepak; Jana, Barun
<i>N</i>-Alkylation of amines with primary/secondary alcohols using a novel cobalt(II) inverse triazolyl-pyridine complex.
Chemical communications (Cambridge, England), 2024, 60, 8581-8584
7133288 CIFC25 H27 N O5 SP -110.6593; 11.0723; 11.354
90.428; 111.448; 105.959
1190.4Li, Meng-Ru; Zheng, Meng-Yao; Wang, Dong-Chao; Guo, Hai-Ming
Pd-catalyzed 5-<i>exo-dig</i> cyclization/etherification cascade of <i>N</i>-propargyl arylamines for the synthesis of polysubstituted furans.
Chemical communications (Cambridge, England), 2024, 60, 7721-7724
7133289 CIFC56 H66 Br8 Cl4 N12 O Pd4C 1 2/c 129.2; 8.5804; 28.6903
90; 93.068; 90
7178Kumar, Shashi; Singh, Dushyant; Rit, Arnab
Cooperativity between metal centers in homobimetallic Pd<sup>II</sup>-NHC complexes: catalytic potential towards hydrodefluorination.
Chemical communications (Cambridge, England), 2024, 60, 7761-7764
7133290 CIFC41 H59 B N4P -19.959; 10.779; 18.206
81.921; 74.267; 88.188
1862.4Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133291 CIFC36 H56 B N5 OP -110.1623; 10.4669; 17.7919
80.944; 74.936; 71.058
1722.96Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133292 CIFC35 H54 B N5P 1 21/n 113.3291; 13.6009; 18.6157
90; 92.442; 90
3371.73Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133293 CIFC35 H52 B Cl2 N5P 1 21/c 123.6475; 15.5802; 18.9468
90; 93.614; 90
6966.74Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133294 CIFC35 H54 B N5P -110.802; 12.3555; 13.8232
76.108; 79.11; 68.167
1652.28Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133295 CIFC36 H56 B N5 OP 1 21/n 19.6634; 19.2539; 18.6478
90; 103.619; 90
3372.02Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133296 CIFC44 H65 B N4P 1 21/n 110.5315; 16.4623; 23.1574
90; 96.209; 90
3991.31Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133297 CIFC240 H152 Au28 Cl48 Cu12 P4 S24P -122.0728; 27.5087; 27.5493
86.596; 78.05; 88.55
16334.9Tang, Shisi; Song, Tongxin; Cai, Xiao; Ding, Weiping; Zhu, Yan
Nitrate electroreduction to ammonia catalysed by atomically precise Au<sub>28</sub>Cu<sub>12</sub> clusters.
Chemical communications (Cambridge, England), 2024, 60, 7785-7788
7133298 CIFC162 H243 Cu28 P3 S18P 1 21/n 119.622; 39.5629; 26.1094
90; 91.255; 90
20263.9Tang, Shisi; Song, Tongxin; Cai, Xiao; Ding, Weiping; Zhu, Yan
Nitrate electroreduction to ammonia catalysed by atomically precise Au<sub>28</sub>Cu<sub>12</sub> clusters.
Chemical communications (Cambridge, England), 2024, 60, 7785-7788
7133299 CIFC40 H41 Cl2 F9 N6 Ni2 O10 S3P 1 21/n 111.118; 20.6674; 21.7121
90; 98.029; 90
4940.1Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133300 CIFC38 H57 F3 N6 Ni2 O17 SP -110.2519; 11.2496; 21.492
77.624; 79.248; 80.429
2357.88Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133301 CIFC74 H82 F6 N12 Ni4 O12 S2P 21 21 2113.7338; 18.9753; 33.797
90; 90; 90
8807.6Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133302 CIFC76 H82 F6 N12 Ni4 O16 S2P 1 21/c 116.1401; 32.5762; 17.5728
90; 111.887; 90
8573.5Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133303 CIFC29 H23 N2 O2 PP 1 21/c 114.8254; 13.4214; 11.2282
90; 93.113; 90
2230.86Huang, Jun; Ban, Caijin; Qin, Jiangping; Xu, Jiali; Gu, Yunqiong; Wei, Liang; Yuan, Jing-Mei; Huang, Guobao
Visible-light promoted radical cascade cyclization of 3-allyl-2-arylquinazolinones for the synthesis of phosphorylated dihydroisoquinolino[1,2-<i>b</i>]quinazolinones.
Chemical communications (Cambridge, England), 2024, 60, 8119-8122
7133304 CIFC39 H51 Cl2 N2 P2P -110.894; 11.6371; 17.3041
86.498; 73.235; 66.584
1923.91Haberstroh, Jan; Taube, Clemens; Fidelius, Jannis; Schulz, Stephen; Israel, Noel; Dmitrieva, Evgenia; Gomila, Rosa M.; Frontera, Antonio; Wolf, Robert; Schwedtmann, Kai; Weigand, Jan J.
A neutral diphosphene radical: synthesis, electronic structure and white phosphorus activation.
Chemical communications (Cambridge, England), 2024, 60, 8537-8540
7133305 CIFC88 H126 Cl4 N4 O2 P4C 1 2/c 114.6385; 34.7552; 18.1897
90; 109.167; 90
8741.26Haberstroh, Jan; Taube, Clemens; Fidelius, Jannis; Schulz, Stephen; Israel, Noel; Dmitrieva, Evgenia; Gomila, Rosa M.; Frontera, Antonio; Wolf, Robert; Schwedtmann, Kai; Weigand, Jan J.
A neutral diphosphene radical: synthesis, electronic structure and white phosphorus activation.
Chemical communications (Cambridge, England), 2024, 60, 8537-8540
7133306 CIFC84 H107 Cl4 F N4 P8P 1 21/c 122.3963; 24.8472; 15.6004
90; 96.933; 90
8617.92Haberstroh, Jan; Taube, Clemens; Fidelius, Jannis; Schulz, Stephen; Israel, Noel; Dmitrieva, Evgenia; Gomila, Rosa M.; Frontera, Antonio; Wolf, Robert; Schwedtmann, Kai; Weigand, Jan J.
A neutral diphosphene radical: synthesis, electronic structure and white phosphorus activation.
Chemical communications (Cambridge, England), 2024, 60, 8537-8540
7133307 CIFC16 H8 N4 O9 ZnP -18.0263; 8.9753; 13.924
95.081; 93.392; 92.034
996.5Dinda, Susanta; Deb, Sourav; Mahato, Bidyadhar; Baitalik, Sujoy; Ghoshal, Debajyoti
Visual detection and efficient capture of hydrogen chloride and ammonia vapours by a sustainable dual emissive metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 8466-8469
7133308 CIFC53.67 H34.45 Cd2 Cl2 N18 O22.05P -111.8103; 12.5965; 13.3862
80.395; 84.225; 78.443
1919.06Jiang, Qiao; Suzuki, Hiroaki; Wada, Yuki; Wang, Xiaohan; Murakami, Yoichi; Matsumoto, Takaya; Usov, Pavel M.; Kawano, Masaki
Magnetic and thermodynamic control of coordination network crystallization using a hexaazaphenalene-based ligand.
Chemical communications (Cambridge, England), 2024, 60, 8236-8239
7133309 CIFC49.22 H31.49 Cd N18 O16.9P c a 2130.3621; 7.9636; 28.193
90; 90; 90
6816.83Jiang, Qiao; Suzuki, Hiroaki; Wada, Yuki; Wang, Xiaohan; Murakami, Yoichi; Matsumoto, Takaya; Usov, Pavel M.; Kawano, Masaki
Magnetic and thermodynamic control of coordination network crystallization using a hexaazaphenalene-based ligand.
Chemical communications (Cambridge, England), 2024, 60, 8236-8239
7133310 CIFC29 H62 N3 Si3P -111.5884; 17.221; 18.536
69.558; 80.011; 82.655
3404.5Kiefer, Fiona J.; Kostenko, Arseni; Holzner, Richard; Inoue, Shigeyoshi
A neutral crystalline imino-substituted silyl radical.
Chemical communications (Cambridge, England), 2024, 60, 8577-8580
7133311 CIFC23 H18 N2 O3P 21 21 216.84; 11.12; 24.67
90; 90; 90
1876Purkait, Anisha; Pal, Surya Veer Singh; Soni, Kaushik; Bhattacharyya, Kalishankar; Jana, Chandan K.
Nitroso-azomethine(ene) reaction enabled annulations of nitrosoarenes, azomethines and alkenes.
Chemical communications (Cambridge, England), 2024, 60, 8541-8544
7133312 CIFC28 H37 P S2 Si3P 1 21/n 117.3438; 7.4997; 23.1443
90; 91.611; 90
3009.27Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133313 CIFC36 H48 Cl P Si4P 1 21/n 116.1335; 13.1016; 16.7859
90; 91.24; 90
3547.28Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133314 CIFC28 H37 P S Si3P 1 21/c 113.1508; 9.7019; 22.7273
90; 101.809; 90
2838.35Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133315 CIFC28 H37 P S Si3P 1 21/c 113.2702; 12.96; 17.3599
90; 107.126; 90
2853.2Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133316 CIFC34 H37 Au F5 P S Si3P -113.8756; 20.1815; 25.941
88.525; 87.728; 75.68
7032.08Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133317 CIFC53 H28 Cl2 N2 O4P 1 21 18.1505; 11.3913; 20.8223
90; 92.329; 90
1931.6Wang, Yuxiang; Liao, Qi; Feng, Yabin; Wang, Yiran; Li, Yunzhi; Meng, Qi
Synthesis and resolution of multi-chiral carbonyl-N embedded hetero[7]helicenes for efficient circularly polarized luminescence.
Chemical communications (Cambridge, England), 2024, 60, 8292-8295
7133318 CIFC64 H54 N2 O4P 6113.1642; 13.1642; 48.25
90; 90; 120
7241.3Wang, Yuxiang; Liao, Qi; Feng, Yabin; Wang, Yiran; Li, Yunzhi; Meng, Qi
Synthesis and resolution of multi-chiral carbonyl-N embedded hetero[7]helicenes for efficient circularly polarized luminescence.
Chemical communications (Cambridge, England), 2024, 60, 8292-8295
7133319 CIFC35 H30 N2 O5P -111.1034; 11.1882; 12.5867
70.9583; 87.9029; 71.6281
1398.89Yadav, Suresh Kumar; Jeganmohan, Masilamani
Co(III)-catalyzed regioselective benzannulation of substituted pyridones with 1,6-diynes <i>via</i> dual C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 8296-8299
7133320 CIFC40 H42 Li2 O4P 1 21/c 110.8476; 10.0967; 15.5113
90; 94.807; 90
1692.9Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133321 CIFC48 H62 K2 O8P 1 21/c 111.1442; 13.0688; 16.746
90; 106.828; 90
2334.47Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133322 CIFC48 H62 Na2 O8P 1 21/c 111.0913; 13.2818; 15.8392
90; 105.146; 90
2252.26Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133323 CIFC83.7 H83.7 Ce K O4.7P -110.2856; 13.0071; 25.713
80.814; 88.212; 78.113
3323.09Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133324 CIFC80 H84 Ce K O8P 1 2/n 115.8469; 10.1787; 21.4308
90; 94.056; 90
3448.15Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133325 CIFC80 H84 K O8 TbP 1 2/n 115.6241; 10.2214; 21.5624
90; 94.643; 90
3432.22Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133326 CIFC76 H74 Li O6 YP 1 21/c 110.33655; 25.4845; 23.3833
90; 96.3298; 90
6122.12Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133327 CIFC100 H116 Cl6 Mg2 O9 Y2P b c m14.8775; 21.4215; 37.4724
90; 90; 90
11942.4Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133328 CIFC53.33 H56 K0.67 La0.67 O5.33P 1 2/n 115.9186; 10.1537; 21.3582
90; 93.633; 90
3445.25Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133329 CIFC176 H184 Mg O12 Y2P 1 21/n 117.52153; 19.2375; 21.05544
90; 92.9279; 90
7087.9Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133330 CIFC96 H108 Na O8 YbP 1 2/n 120.1809; 15.78844; 25.03591
90; 90.51; 90
7976.75Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133331 CIFC19 H23 NP n m a11.2368; 7.0029; 19.2578
90; 90; 90
1515.4Yang, Fang; Li, Heyang; Li, Huijie; He, Xiaoming
Manipulation of 1D and 2D self-assembly <i>via</i> geometry modulation of adamantane isocyanide Pt(II) complexes.
Chemical communications (Cambridge, England), 2024, 60, 8605-8608
7133332 CIFC28 H30 N2P 1 21/c 16.7908; 19.6373; 16.4833
90; 90.029; 90
2198.1Yang, Fang; Li, Heyang; Li, Huijie; He, Xiaoming
Manipulation of 1D and 2D self-assembly <i>via</i> geometry modulation of adamantane isocyanide Pt(II) complexes.
Chemical communications (Cambridge, England), 2024, 60, 8605-8608
7133333 CIFC26 H24 B Cr2 N4 Na O13P c a 2123.3656; 9.1918; 31.7925
90; 90; 90
6828.14Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133334 CIFC24 H32 B Cr N4 Na O8P -19.8572; 12.1418; 12.9109
100.325; 96.817; 95.944
1497.09Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133335 CIFC308 H280 B8 Cr8 N32 O39 P8P -116.6054; 18.2464; 27.5141
93.222; 99.544; 113.692
7458.23Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133336 CIFC104 H152 B4 Cr4 N16 Na4 O31P 1 21/n 117.5473; 20.8549; 35.3881
90; 102.2; 90
12657.7Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133337 CIFC37 H28 N4 O2P -19.5486; 9.8277; 16.757
103.234; 103.776; 97.299
1459Balasubramani, Alagesan; Sudarshana, K. A.; Kushwaha, Roli; Chakravarty, Sumana; Pabbaraja, Srihari; Mehta, Goverdhan
One flask cascade approach to a complex pyrano[2,3-<i>c</i>]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling.
Chemical communications (Cambridge, England), 2024, 60, 8443-8446
7133338 CIFC41 H32 N4 O2P -19.341; 11.471; 15.177
88.237; 77.033; 83.309
1574Balasubramani, Alagesan; Sudarshana, K. A.; Kushwaha, Roli; Chakravarty, Sumana; Pabbaraja, Srihari; Mehta, Goverdhan
One flask cascade approach to a complex pyrano[2,3-<i>c</i>]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling.
Chemical communications (Cambridge, England), 2024, 60, 8443-8446
7133339 CIFC37 H26 Cl2 N4 O2P -19.724; 12.297; 13.872
103.225; 106.099; 98.327
1512.5Balasubramani, Alagesan; Sudarshana, K. A.; Kushwaha, Roli; Chakravarty, Sumana; Pabbaraja, Srihari; Mehta, Goverdhan
One flask cascade approach to a complex pyrano[2,3-<i>c</i>]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling.
Chemical communications (Cambridge, England), 2024, 60, 8443-8446
7133340 CIFC47 H82 N4 Si4 YbP b c a17.9657; 22.4892; 28.4392
90; 90; 90
11490.4Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133341 CIFC50 H88 N4 Si4 YbP 1 21/c 114.1534; 17.7808; 22.4677
90; 100.898; 90
5552.2Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133342 CIFC46 H83 N5 Si4 YbP 1 21/n 113.2397; 22.4875; 18.0354
90; 105.208; 90
5181.6Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133343 CIFC50 H90 N4 Si4 YbP b c a18.0881; 22.6537; 26.9902
90; 90; 90
11059.6Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133344 CIFC34.06 H68.23 N4 O0.06 S2 Si4 YbP -115.4962; 17.7037; 19.308
78.382; 69.436; 69.691
4632.04Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133345 CIFC37 H39 N3 TiP b c a16.6089; 14.6227; 24.9167
90; 90; 90
6051.44Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133346 CIFC30 H31 N3 TiP 1 21/c 111.5575; 17.8865; 11.9883
90; 103.609; 90
2408.68Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133347 CIFC45 H55 N3 TiP -110.1395; 12.8171; 16.6592
71.421; 85.313; 66.806
1883.94Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133348 CIFC39 H53 N3 TiP -111.0602; 12.062; 14.3315
77.339; 77.207; 70.619
1736.62Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133349 CIFC17 H22 B Br N2 O4P 21 21 218.2775; 8.4391; 27.6673
90; 90; 90
1932.69Ankudinov, Nikita M.; Komarova, Alina A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Danshina, Anastasia A.; Perekalin, Dmitry S.
Synthesis of chiral boranes <i>via</i> asymmetric insertion of carbenes into B-H bonds catalyzed by the rhodium(I) diene complex.
Chemical communications (Cambridge, England), 2024, 60, 8601-8604
7133350 CIFC139 H103 Cd6 N13 O33P -112.2239; 12.3893; 30.5039
80.911; 84.233; 61.359
4001.9Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133351 CIFC29 H23 Cd N4 O5P -19.8998; 10.3818; 13.7847
85.545; 75.783; 70.838
1297.27Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133352 CIFC108 H92 Cd4 N12 O24C 1 2/c 126.0598; 8.2468; 22.9568
90; 93.487; 90
4924.5Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133353 CIFC100 H92 Cd4 N12 O24C 1 2/c 126.241; 7.6898; 23.0522
90; 91.71; 90
4649.6Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133354 CIFC41 H32 Cd N4 O10P -19.0027; 12.5556; 16.1594
82.397; 84.317; 87.262
1800.5Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133355 CIFC14 H8 B ClP 1 21 18.5508; 3.8729; 15.8451
90; 102.727; 90
511.84Zacharias, Harie; Begum, Ayesha; Han, Jianhua; Bartholome, Tyler A.; Marder, Todd B.; Martin, Caleb D.
Synthesis of phenanthrylboroles and formal nitrene insertion to access azaborapyrenes.
Chemical communications (Cambridge, England), 2024, 60, 8740-8743
7133356 CIFC21 H15 B Cl NP 21 21 215.4556; 16.6414; 17.5759
90; 90; 90
1595.7Zacharias, Harie; Begum, Ayesha; Han, Jianhua; Bartholome, Tyler A.; Marder, Todd B.; Martin, Caleb D.
Synthesis of phenanthrylboroles and formal nitrene insertion to access azaborapyrenes.
Chemical communications (Cambridge, England), 2024, 60, 8740-8743
7133357 CIFC20 H16 O S2P 1 21/n 110.0077; 11.6105; 14.5031
90; 99.121; 90
1663.87Hu, Xinwei; Zhong, Kaihui; Ruan, Zhixiong
Tunable electrochemical diverse sulfurization of sulfoxonium ylides with disulfides.
Chemical communications (Cambridge, England), 2024, 60, 8573-8576
7133358 CIFC16 H11 F5 O2 S2P -19.0497; 9.8617; 17.5484
92.637; 91.848; 95.942
1554.97Hu, Xinwei; Zhong, Kaihui; Ruan, Zhixiong
Tunable electrochemical diverse sulfurization of sulfoxonium ylides with disulfides.
Chemical communications (Cambridge, England), 2024, 60, 8573-8576
7133359 CIFC14 H8 N2 O8P -14.9931; 5.055; 12.7089
87.739; 85.844; 80.408
315.34Omura, Takumi; Morisako, Shogo; Isoda, Kyosuke
Amino acid-appended pyromellitic diimide liquid materials, their photoluminescence, and the thermal response that turns the photoluminescence off.
Chemical communications (Cambridge, England), 2024, 60, 9352-9355
7133360 CIFC30 H28 N2 O8P 1 21 17.5542; 7.0242; 24.7028
90; 96.948; 90
1301.16Omura, Takumi; Morisako, Shogo; Isoda, Kyosuke
Amino acid-appended pyromellitic diimide liquid materials, their photoluminescence, and the thermal response that turns the photoluminescence off.
Chemical communications (Cambridge, England), 2024, 60, 9352-9355
7133361 CIFC47 H65 F9 N10 O16P 16.7234; 10.105; 19.638
91.057; 90.07; 93.418
1331.6Cayrou, Chloé; Walrant, Astrid; Ravault, Delphine; Guitot, Karine; Noinville, Sylvie; Sagan, Sandrine; Brigaud, Thierry; Gonzalez, Simon; Ongeri, Sandrine; Chaume, Grégory
Incorporation of CF<sub>3</sub>-pseudoprolines into polyproline type II foldamers confers promising biophysical features.
Chemical communications (Cambridge, England), 2024, 60, 8609-8612
7133362 CIFC16 H10 O2 SP -17.6112; 8.5345; 9.9571
111.229; 102.154; 93.29
583.02Reid, Amelia G.; Zelenke, Ethan A.; Moberg, Megan E.; Dickie, Diane A.; Machan, Charles W.
Improving co-electrocatalytic carbon dioxide reduction by optimizing the relative potentials of the redox mediator and catalyst.
Chemical communications (Cambridge, England), 2024, 60, 8208-8211
7133363 CIFC22 H21 Cl Cu N6 O6P 1 21/n 110.905; 19.645; 11.608
90; 104.342; 90
2409Kaur, Simarjeet; Das, Avijit; Velasco, Lucia; Sauvan, Maxime; Bera, Moumita; Ugale, Ashok; Charisiadis, Asterios; Moonshiram, Dooshaye; Paria, Sayantan
Spectroscopic characterization and reactivity studies of a copper(II) iminoxyl radical complex.
Chemical communications (Cambridge, England), 2024, 60, 9934-9937
7133364 CIFC25 H19 N O3P 1 21/c 111.828; 14.9837; 11.0984
90; 106.25; 90
1888.4Chi, Dongmei; Qi, Hongbo; Wang, Leming; Chen, Shufeng
Pd-Catalyzed cascade Heck cyclization/carbonylation of indoles with aryl formates: enantioselective construction of indolo[2,1-<i>a</i>]isoquinolines.
Chemical communications (Cambridge, England), 2024, 60, 8613-8616
7133365 CIFC68 H40 N4 O32 Zr6F m m m17.936; 30.464; 31.068
90; 90; 90
16976Li, Fugang; Huang, Jinyi; Meng, Yuxuan; Li, Ji; Zhang, Liangliang; Sheng, Daopeng
<i>In situ</i> confinement of ultra-small metal nanoparticles in redox-active zirconium MOFs for catalysis.
Chemical communications (Cambridge, England), 2024, 60, 8708-8711
7133366 CIFC68.5 H40 Eu6 F8 N4 O24.5F m m m19.893; 30.475; 31.958
90; 90; 90
19374Li, Fugang; Huang, Jinyi; Meng, Yuxuan; Li, Ji; Zhang, Liangliang; Sheng, Daopeng
<i>In situ</i> confinement of ultra-small metal nanoparticles in redox-active zirconium MOFs for catalysis.
Chemical communications (Cambridge, England), 2024, 60, 8708-8711
7133367 CIFC52 H48 Fe2 N4 S4P -111.2216; 12.4643; 19.1311
72.756; 80.477; 67.034
2349.2Spielvogel, Kyle D.; Campbell, Emily J.; Chowdhury, Sabyasachi Roy; Benner, Florian; Demir, Selvan; Hatzis, Gillian P.; Petras, Hayley R.; Sembukuttiarachchige, Dunya; Shepherd, James J.; Thomas, Christine M.; Vlaisavljevich, Bess; Daly, Scott R.
Modulation of Fe-Fe distance and spin in diiron complexes using tetradentate ligands with different flanking donors.
Chemical communications (Cambridge, England), 2024, 60, 8399-8402
7133368 CIFC40 H36 Fe2 N4 S4P 1 21/n 114.7925; 12.1411; 20.679
90; 93.443; 90
3707.2Spielvogel, Kyle D.; Campbell, Emily J.; Chowdhury, Sabyasachi Roy; Benner, Florian; Demir, Selvan; Hatzis, Gillian P.; Petras, Hayley R.; Sembukuttiarachchige, Dunya; Shepherd, James J.; Thomas, Christine M.; Vlaisavljevich, Bess; Daly, Scott R.
Modulation of Fe-Fe distance and spin in diiron complexes using tetradentate ligands with different flanking donors.
Chemical communications (Cambridge, England), 2024, 60, 8399-8402
7133369 CIFC53 H57 Fe2 N8P 1 21/c 114.128; 17.7302; 18.8223
90; 101.994; 90
4611.9Spielvogel, Kyle D.; Campbell, Emily J.; Chowdhury, Sabyasachi Roy; Benner, Florian; Demir, Selvan; Hatzis, Gillian P.; Petras, Hayley R.; Sembukuttiarachchige, Dunya; Shepherd, James J.; Thomas, Christine M.; Vlaisavljevich, Bess; Daly, Scott R.
Modulation of Fe-Fe distance and spin in diiron complexes using tetradentate ligands with different flanking donors.
Chemical communications (Cambridge, England), 2024, 60, 8399-8402
7133370 CIFC94 H102 Fe4 N16P -114.495; 17.19; 20.268
68.265; 89.15; 87.363
4686Spielvogel, Kyle D.; Campbell, Emily J.; Chowdhury, Sabyasachi Roy; Benner, Florian; Demir, Selvan; Hatzis, Gillian P.; Petras, Hayley R.; Sembukuttiarachchige, Dunya; Shepherd, James J.; Thomas, Christine M.; Vlaisavljevich, Bess; Daly, Scott R.
Modulation of Fe-Fe distance and spin in diiron complexes using tetradentate ligands with different flanking donors.
Chemical communications (Cambridge, England), 2024, 60, 8399-8402
7133371 CIFC32 H44 N2 O2P 21 21 218.7963; 9.5198; 34.7853
90; 90; 90
2912.89Bando, Masayoshi; Fortino, Mariagrazia; Pietropaolo, Adriana; Shichibu, Yukatsu; Konishi, Katsuaki; Nakano, Tamaki
Molecular ordering-enhanced circularly polarized luminescence of chiral 1,10-phenanthroline derivatives.
Chemical communications (Cambridge, England), 2024, 60, 8625-8628
7133372 CIFC38 H38 N O2P 1 21/c 118.2704; 10.4138; 18.749
90; 118.769; 90
3126.95Ali, Amjad; Harit, Harish K.; Behera, Chandana; Singh, Ravi P.
A diastereoselective strategy for dihydrophenanthrene-fused spirooxindoles <i>via</i> [1,2]-phospha-Brook rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 8904-8907
7133373 CIFC31 H26 F N2 O P PdP -19.6832; 11.7011; 13.0161
73.358; 74.524; 66.061
1272.21Jabbarpoor, Maryam; LeBlanc, Jesse; Chen, Zichuan; Cadwallader, Dusty; Le, Christine M.
Pd-catalyzed Suzuki-type cross-coupling of 2-pyridyl carbamoyl fluorides.
Chemical communications (Cambridge, England), 2024, 60, 8700-8703
7133374 CIFC35 H34 Cl N2 O3 P PdP 1 21/n 111.026; 16.8504; 17.4371
90; 99.551; 90
3194.8Jabbarpoor, Maryam; LeBlanc, Jesse; Chen, Zichuan; Cadwallader, Dusty; Le, Christine M.
Pd-catalyzed Suzuki-type cross-coupling of 2-pyridyl carbamoyl fluorides.
Chemical communications (Cambridge, England), 2024, 60, 8700-8703
7133375 CIFC314 H312 Cl3 F10 N49 O47P -123.7615; 24.0825; 35.9358
101.204; 91.4858; 111.906
18605.5Yao, Chenhao; Gole, Bappaditya; Bui, Anh Thy; Kauffmann, Brice; Huc, Ivan; McClenaghan, Nathan D.; Ferrand, Yann
Photon-gated foldaxane assembly/disassembly.
Chemical communications (Cambridge, England), 2024, 60, 8415-8418
7133376 CIFC82 H88 Cl F18 Fe2 N19 O16 S6P 1 21/n 117.5489; 15.0572; 36.9438
90; 94.949; 90
9725.5Ríos, Pablo; See, Matthew S.; Gonzalez, Oscar; Handford, Rex C.; Nicolay, Amélie; Rao, Guodong; Britt, R. David; Bediako, D. Kwabena; Tilley, T. Don
Iron homo- and heterobimetallic complexes supported by a symmetrical dinucleating ligand.
Chemical communications (Cambridge, England), 2024, 60, 8912-8915
7133377 CIFC62 H61 N16 O1.5C 1 2 124.0364; 14.7281; 19.756
90; 126.263; 90
5639.2Ríos, Pablo; See, Matthew S.; Gonzalez, Oscar; Handford, Rex C.; Nicolay, Amélie; Rao, Guodong; Britt, R. David; Bediako, D. Kwabena; Tilley, T. Don
Iron homo- and heterobimetallic complexes supported by a symmetrical dinucleating ligand.
Chemical communications (Cambridge, England), 2024, 60, 8912-8915
7133378 CIFC30 H28 Cl2 Fe N8C 1 2/c 131.3189; 12.0713; 16.0669
90; 107.591; 90
5790.2Ríos, Pablo; See, Matthew S.; Gonzalez, Oscar; Handford, Rex C.; Nicolay, Amélie; Rao, Guodong; Britt, R. David; Bediako, D. Kwabena; Tilley, T. Don
Iron homo- and heterobimetallic complexes supported by a symmetrical dinucleating ligand.
Chemical communications (Cambridge, England), 2024, 60, 8912-8915
7133379 CIFC96 H90 Cl2 F6 Fe2 N26 O6 S2P -114.0576; 19.146; 22.1777
78.52; 74.856; 72.035
5435.1Ríos, Pablo; See, Matthew S.; Gonzalez, Oscar; Handford, Rex C.; Nicolay, Amélie; Rao, Guodong; Britt, R. David; Bediako, D. Kwabena; Tilley, T. Don
Iron homo- and heterobimetallic complexes supported by a symmetrical dinucleating ligand.
Chemical communications (Cambridge, England), 2024, 60, 8912-8915
7133380 CIFC101.51 H98.26 Cl2 F6 Fe Mn N28.75 O6 S2P -114.1048; 19.0576; 22.1206
78.592; 75.168; 71.179
5397.34Ríos, Pablo; See, Matthew S.; Gonzalez, Oscar; Handford, Rex C.; Nicolay, Amélie; Rao, Guodong; Britt, R. David; Bediako, D. Kwabena; Tilley, T. Don
Iron homo- and heterobimetallic complexes supported by a symmetrical dinucleating ligand.
Chemical communications (Cambridge, England), 2024, 60, 8912-8915
7133381 CIFC184 H142 N18 Ni2 O12C 1 2/c 131.418; 40.637; 19.4953
90; 117.411; 90
22096He, Yixing; Yu, Zhi; Jiang, Yanzi; Zhu, Jinjie; Yao, Selina X.; Liang, Wenjie; Diederich, François; Saunders, Martin; Xu, Hai
A H<sub>2</sub>@C<sub>60</sub><sup>1</sup>H NMR probe for sensitively detecting the supramolecular interactions between a molecular tweezer and C<sub>60</sub>.
Chemical communications (Cambridge, England), 2024, 60, 8716-8719
7133382 CIFC27 H31 N O4 SP 21 21 216.2369; 10.018; 39.109
90; 90; 90
2443.6Singh, Suraj; Kumar, Rohtash; Dubey, Navneet Nandgopal; Appayee, Chandrakumar
Synthesis and application of chiral <i>cis</i>-2,5-disubstituted pyrrolidine organocatalysts.
Chemical communications (Cambridge, England), 2024, 60, 8768-8771
7133383 CIFC21 H21 Cl N2 O4P 21 21 215.1998; 15.781; 24.305
90; 90; 90
1994.4Singh, Suraj; Kumar, Rohtash; Dubey, Navneet Nandgopal; Appayee, Chandrakumar
Synthesis and application of chiral <i>cis</i>-2,5-disubstituted pyrrolidine organocatalysts.
Chemical communications (Cambridge, England), 2024, 60, 8768-8771
7133384 CIFC16 H17 N O2 S2P 1 21/c 118.822; 9.4151; 9.3683
90; 94.291; 90
1655.5Li, Xuejian; Liu, Qinglong; Song, Wangze
Chemical fixation of CO<sub>2</sub>/CS<sub>2</sub> to access iodoallenyl oxazolidinones and allenyl thiazolidine-thiones.
Chemical communications (Cambridge, England), 2024, 60, 8756-8759
7133385 CIFC285 H186 Ag6 N12 O36 P6 Ti4C 1 2/c 178.8953; 22.1894; 35.6493
90; 94.371; 90
62227.5Yuan, Yuan; Zhang, Dong-Hui; Li, Qiao-Hong; Chen, Shu-Mei; He, Yan-Ping; Zhang, Jian
Combining Ti<sub>4</sub>(embonate)<sub>6</sub> anionic cages and π-conjugated coordination cations for highly effective optical limiting.
Chemical communications (Cambridge, England), 2024, 60, 8748-8751
7133386 CIFC212 H132 Ag2 N4 O36 P4 Ti4P 41 21 220.4503; 20.4503; 54.8956
90; 90; 90
22958.2Yuan, Yuan; Zhang, Dong-Hui; Li, Qiao-Hong; Chen, Shu-Mei; He, Yan-Ping; Zhang, Jian
Combining Ti<sub>4</sub>(embonate)<sub>6</sub> anionic cages and π-conjugated coordination cations for highly effective optical limiting.
Chemical communications (Cambridge, England), 2024, 60, 8748-8751
7133387 CIFC294 H224 Ag8 N8 O36 P8 Ti4I 1 2/a 135.6145; 22.6414; 47.7519
90; 110.16; 90
36146.3Yuan, Yuan; Zhang, Dong-Hui; Li, Qiao-Hong; Chen, Shu-Mei; He, Yan-Ping; Zhang, Jian
Combining Ti<sub>4</sub>(embonate)<sub>6</sub> anionic cages and π-conjugated coordination cations for highly effective optical limiting.
Chemical communications (Cambridge, England), 2024, 60, 8748-8751
7133388 CIFH237 K25 Mn11 Nb62 O330 Te15P -122.62; 24.412; 38.496
98.666; 100.99; 112.911
18617Wu, Ping-Xin; Chen, Chun-Xia; Sun, Yan-Qiong; Zheng, Shou-Tian
A water-soluble mixed-valent {Mn<sub>11</sub>} cluster embedded heteropolyoxoniobate with magnetic properties.
Chemical communications (Cambridge, England), 2024, 60, 8888-8891
7133389 CIFC15 H16 N6 Ni O4C 1 2/c 113.559; 9.666; 13.263
90; 111.25; 90
1620.1Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133390 CIFC15 H16 N6 Ni O4C 1 2/c 113.643; 9.66; 13.321
90; 111.02; 90
1638.8Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133391 CIFC15 H16 N6 Ni O4C 1 c 113.5175; 9.6; 13.278
90; 110.466; 90
1614.3Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133392 CIFC15 H16 N6 Ni O4C 1 c 113.385; 9.559; 13.218
90; 110.52; 90
1583.9Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133393 CIFC15 H16 N6 Ni O4C 1 c 113.709; 9.662; 13.361
90; 110.45; 90
1658.2Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133394 CIFC15 H16 N6 Ni O4C 1 c 113.75; 9.663; 13.387
90; 110.53; 90
1665.7Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133395 CIFC15 H16 N6 Ni O4C 1 c 113.232; 9.508; 13.132
90; 110.46; 90
1547.9Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133396 CIFC15 H16 N6 Ni O4C 1 c 113.026; 9.45; 13.021
90; 110.4; 90
1502.3Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133397 CIFC15 H16 N6 Ni O4P -119.686; 9.307; 12.765
90.02; 106.67; 105.24
2154.4Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133398 CIFC15 H16 N6 Ni O4C 1 c 112.836; 9.391; 12.908
90; 108.56; 90
1475Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133399 CIFC15 H16 N6 Ni O4P -119.543; 9.269; 12.708
89.99; 106.56; 105.39
2120.3Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133400 CIFC15 H16 N6 Ni O4P -112.306; 9.1663; 12.558
90.212; 105.34; 87.125
1364.3Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133401 CIFC15 H16 N6 Ni O4P -112.098; 9.0718; 12.404
90.129; 104.909; 87.038
1313.7Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133402 CIFC15 H16 N6 Ni O4P -112.208; 9.126; 12.491
90.205; 105.14; 87.019
1341.4Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133403 CIFC15 H16 N6 Ni O4P -119.527; 9.2591; 12.693
90.057; 106.512; 105.351
2114.6Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133404 CIFC15 H16 N6 Ni O4P -112.369; 9.1988; 12.599
90.252; 105.495; 87.182
1379.7Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133405 CIFC15 H16 N6 Ni O4P -112.396; 9.204; 12.618
90.26; 105.54; 87.17
1385.2Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133406 CIFC15 H16 N6 Ni O4P -119.77; 9.3295; 12.796
90.044; 106.801; 104.937
2175.8Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133407 CIFC15 H16 N6 Ni O4C 1 c 113.295; 9.5267; 13.169
90; 110.6; 90
1561.3Potempa, Kinga; Paliwoda, Damian; Jarzembska, Katarzyna N.; Kamiński, Radosław; Krówczyński, Adam; Borowski, Patryk; Hanfland, Michael
Pressure-induced single-crystal-to-single-crystal nitrite ligand isomerisation accompanied by a piezochromic effect.
Chemical communications (Cambridge, England), 2024, 60, 9194-9197
7133408 CIFC10 H7 F3 O2P 1 21 18.51; 4.956; 11.481
90; 106.91; 90
463.3Kazi, Ayazoddin Aunoddin; Manjuladevi, Nadimpalli; Kumar, Salla Suresh; Sharma, Anamika; Singh, L. Ravithej
A quick access to CF<sub>3</sub>-containing functionalized benzofuranyl, benzothiophene and indolyl heterocycles under catalyst-free conditions.
Chemical communications (Cambridge, England), 2024, 60, 9376-9379
7133409 CIFC11 H9 Br F3 N O3 SP n a 215.4629; 21.481; 11.2799
90; 90; 90
1323.7Kazi, Ayazoddin Aunoddin; Manjuladevi, Nadimpalli; Kumar, Salla Suresh; Sharma, Anamika; Singh, L. Ravithej
A quick access to CF<sub>3</sub>-containing functionalized benzofuranyl, benzothiophene and indolyl heterocycles under catalyst-free conditions.
Chemical communications (Cambridge, England), 2024, 60, 9376-9379
7133410 CIFC161.8 H256.4 Br10 N10 O37P 1 21/c 126.50453; 14.53119; 25.82392
90; 114.266; 90
9067.12Gao, Tu-Nan; Yang, Zhen; Goed, Jesse M. S.; Zuilhof, Han; Miloserdov, Fedor M.
Rim-differentiated pillar[5]arene-modified surfaces for rapid PFOA/PFOS detection.
Chemical communications (Cambridge, England), 2024, 60, 9789-9792
7133411 CIFC21 H16 O3P 1 21 17.48375; 23.7768; 8.95801
90; 94.0554; 90
1589.99Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133412 CIFC44 H34 Br2 O4P 1 21/c 128.1188; 7.6926; 15.6637
90; 92.223; 90
3385.61Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133413 CIFC20 H13 Br O2P 21 21 218.0085; 8.9848; 21.0224
90; 90; 90
1512.66Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133414 CIFC21 H15 Br OP b c a15.1076; 10.0376; 20.6682
90; 90; 90
3134.2Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133415 CIFC21 H15 Br O2P 1 21 18.8697; 22.6968; 8.963
90; 114.336; 90
1644.05Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133416 CIFC22 H17 Br OP 21 21 215.595; 10.2307; 29.7158
90; 90; 90
1700.96Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133417 CIFC23 H21 Br O SiP 21 21 218.6383; 12.6159; 17.6123
90; 90; 90
1919.39Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133418 CIFC21 H15 Br OP 21 21 217.8805; 11.2373; 17.8564
90; 90; 90
1581.28Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133419 CIFC27 H19 Br OP 1 21 18.7121; 8.882; 13.2952
90; 98.023; 90
1018.72Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133420 CIFC22 H17 Br OP 21 21 217.6693; 13.0042; 17.0867
90; 90; 90
1704.11Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133421 CIFC27 H18 Br N OP 21 21 218.151; 12.057; 19.765
90; 90; 90
1942Liu, Zi-Li; Wang, Yu-Xin; Yang, Zi-Qi; Yang, Yu-Heng; Liu, Yin-Ping; Hao, Wen-Juan; Jiang, Bo
Construction of central and axial chirality <i>via</i> Pd(II)/Bim-catalyzed asymmetric dearomative Michael reaction of polycyclic tropones.
Chemical communications (Cambridge, England), 2024, 60, 8908-8911
7133422 CIFC58 H62 N4 O2.5P -112.2185; 12.7948; 16.259
95.049; 93.58; 102.198
2466.2Nanda, Gyana Prakash; Chand, Savita; Rajamanickam, Suresh; Rajamalli, Pachaiyappan
Single-component TADF gels: study of the positional isomer effect on gelation and morphological effect on conductivity.
Chemical communications (Cambridge, England), 2024, 60, 9234-9237
7133423 CIFC24 H30 B PP -19.6433; 10.8253; 10.9474
75.97; 65.639; 70.947
976.29Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133424 CIFC23 H28 B PP 21 21 217.1446; 12.0021; 21.825
90; 90; 90
1871.5Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133425 CIFC26 H37 B2 O PP -19.1755; 11.3395; 12.5538
78.769; 77.719; 67.258
1167.84Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133426 CIFC19 H36 B PP b c a15.2898; 12.3183; 19.1817
90; 90; 90
3612.8Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133427 CIFC29 H53.5 Au B Cl N2 O0.75 PP -17.1927; 11.9175; 19.131
78.6195; 86.0612; 86.5573
1602.04Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133428 CIFC56 H102 B2 N4 O0.5 P2 PtP -110.6781; 10.9251; 12.9656
101.27; 98.789; 90.25
1465.06Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133429 CIFC20 H38 B PP 1 21/c 113.62; 10.375; 13.264
90; 93.932; 90
1869.9Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133430 CIFC26 H46 B N2 PP -111.1805; 11.2066; 11.5832
69.782; 80.362; 74.668
1308.78Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133431 CIFC15 H11 B F3 N OP 1 21/n 19.3925; 12.469; 11.765
90; 106.136; 90
1323.6Panigrahi, Pritishree; Ghosh, Subhendu; Khandelia, Tamanna; Tripathi, Gyanesh; Mandal, Raju; Patel, Bhisma K.
Harnessing reductive BF<sub>2</sub>-complexation <i>via</i> Ru(II)-catalyzed N-O cleavage of isoxazoles.
Chemical communications (Cambridge, England), 2024, 60, 9109-9112
7133432 CIFC18 H14 F N O2P -19.277; 9.5602; 9.7665
104.289; 110.312; 107.388
713.26Zhang, Jinhui; Mao, Lihua; Liu, Chao; Tan, Xiangwen; Wu, Jiahao; Wei, Xuefeng; Wu, Wanqing; Jiang, Huanfeng
Palladium-catalyzed 1,1-aminoxylation of 3-butenoic acid with 2-alkynylanilines.
Chemical communications (Cambridge, England), 2024, 60, 9404-9407
7133433 CIFC18 H19 N3 O4P 1 21/c 111.6692; 12.8126; 11.3946
90; 97.665; 90
1688.42Husbands, David R.; Booth, Elisha M.; Donaldson, Niall W. B.; Kapur, Nikil; Willans, Rebecca M.; Willans, Charlotte E.
Electrochemical removal of toxic metals from reaction media following catalysis.
Chemical communications (Cambridge, England), 2024, 60, 8876-8879
7133434 CIFC26 H31 Cl3 N6 OP 1 21/n 112.1807; 11.6269; 19.3144
90; 102.231; 90
2673.29Choi, Taehyeon; Kim, Heechan; Kim, Younghun; Lee, Dongwhan
Urea-fused and π-extended single-benzene fluorophores with ultralarge Stokes shifts.
Chemical communications (Cambridge, England), 2024, 60, 9105-9108
7133435 CIFC38 H44 F2 N2 O4P 1 21/c 18.6691; 21.3606; 18.6802
90; 99.169; 90
3414.9Roy, Barnali; Avasare, Vidya; Sarkar, Debayan
Tribromide enabled step-up generation of spirolactams from esters employing oxidative dearomatization of arenols.
Chemical communications (Cambridge, England), 2024, 60, 9206-9209
7133436 CIFC21 H17 N O4P 1 21/n 114.2969; 6.8015; 18.834
90; 112.036; 90
1697.6Meena, Shivam A.; Thakur, Deepika; Nandy, Abhijit; Ranjan, Rahul; Rai, Anubhav; Banerjee, Shibdas; Verma, Akhilesh K.
Transition-metal free, radical oxidation of 1,6-enyne cyclopropanation: synthesis of aza-bicyclo[4.1.0]heptane derivatives.
Chemical communications (Cambridge, England), 2024, 60, 9230-9233
7133437 CIFC19 H15 N O3P 1 21 110.275; 6.3644; 12.1715
90; 112.449; 90
735.63Meena, Shivam A.; Thakur, Deepika; Nandy, Abhijit; Ranjan, Rahul; Rai, Anubhav; Banerjee, Shibdas; Verma, Akhilesh K.
Transition-metal free, radical oxidation of 1,6-enyne cyclopropanation: synthesis of aza-bicyclo[4.1.0]heptane derivatives.
Chemical communications (Cambridge, England), 2024, 60, 9230-9233
7133438 CIFC18 H15 N O3P -110.6199; 10.8504; 15.1555
103.773; 97.032; 114.529
1493.92Meena, Shivam A.; Thakur, Deepika; Nandy, Abhijit; Ranjan, Rahul; Rai, Anubhav; Banerjee, Shibdas; Verma, Akhilesh K.
Transition-metal free, radical oxidation of 1,6-enyne cyclopropanation: synthesis of aza-bicyclo[4.1.0]heptane derivatives.
Chemical communications (Cambridge, England), 2024, 60, 9230-9233
7133439 CIFC22 H15 F N2P -18.757; 9.973; 11.506
103.314; 100.861; 113.664
850Zhou, Honggui; Li, Zhefeng; Chen, Juehong; Zhou, Si; Wang, Xinyu; Zhang, Linwei; Chen, Jiuxi; Lv, Ningning
Synthesis of polysubstituted pyridazines <i>via</i> Cu-mediated C(sp<sup>3</sup>)-C(sp<sup>3</sup>) coupling/annulation of saturated ketones with acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 9546-9549
7133440 CIFC70 H66 Li2 O2 P4 Se2P 1 21/c 115.7265; 9.5019; 20.4394
90; 97.157; 90
3030.5Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133441 CIFC46 H66 Li2 N6 O2 P2 Se2C 1 2 123.832; 9.4158; 11.2461
90; 103.328; 90
2455.63Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133442 CIFC70 H66 Li2 O2 P4 S2P 1 21/c 114.7042; 11.1057; 18.8325
90; 106.001; 90
2956.21Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133443 CIFC36 H36 Li2 O6 P2P -114.2502; 15.4854; 15.5126
90.527; 91.99; 100.3
3365.56Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133444 CIFC30 H33 B O2P 1 21/n 19.248; 12.097; 22.961
90; 100.211; 90
2528Sun, Fei; Zheng, Yiyi; Wu, Mingxia; Ji, Hongsen; Jiang, Zhongyao; Liu, Chenglin; Wu, Xin-Xing
Three-component cascade carbopalladation/Heck cyclization/borylation: facile access to boryl-functionalized indenes.
Chemical communications (Cambridge, England), 2024, 60, 8075-8078
7133445 CIFC31 H29 B F6 O2P -18.649; 13.234; 13.312
107.837; 95.839; 96.84
1424.7Sun, Fei; Zheng, Yiyi; Wu, Mingxia; Ji, Hongsen; Jiang, Zhongyao; Liu, Chenglin; Wu, Xin-Xing
Three-component cascade carbopalladation/Heck cyclization/borylation: facile access to boryl-functionalized indenes.
Chemical communications (Cambridge, England), 2024, 60, 8075-8078
7133446 CIFC48 H60 Br Cl4 N4 O2C 1 2/c 112.433; 20.341; 18.392
90; 90.85; 90
4650.8Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133447 CIFC51 H62 Cl3 N4 O2P 1 21/n 110.837; 21.536; 22.074
90; 97.33; 90
5109.7Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133448 CIFC38 H56 Cl N4 O3P 1 21/n 111.588; 18.52; 17.078
90; 92.11; 90
3662.6Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133449 CIFC37 H54 Cl N4 O3P -111.704; 16.986; 19.521
87.59; 88.68; 81.55
3834.8Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133450 CIFC51 H66 Cl N4 O3C 1 2/c 124.135; 22.011; 21.701
90; 122.41; 90
9733Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133451 CIFC62 H51.35 N6 O6 S2P 110.2217; 11.1542; 13.1904
95.111; 94.018; 111.248
1387.58Choudhary, Kavita; Deshpande, Akanksha Santosh; Singh, Vinod K.
Ag(I)-catalyzed asymmetric (2+4) annulation reaction of 5-alkenyl thiazolones: synthesis of enantioenriched spiro[cyclohexenamines-thiazolones].
Chemical communications (Cambridge, England), 2024, 60, 9062-9065
7133452 CIFC40 H40 Cu I3 P2P 1 21/c 119.087; 13.1972; 17.36
90; 116.135; 90
3925.8Liu, Xia; Li, Bohan; Jin, Jiance; Yang, Lin; Xia, Zhiguo; Xu, Yan
Solvent-induced structural regulation and luminescence switching of hybrid copper(I) halides for encryption and anti-counterfeiting applications.
Chemical communications (Cambridge, England), 2024, 60, 9034-9037
7133453 CIFC20 H20 Cu I2 PP 1 21/c 18.679; 20.4707; 11.8536
90; 96.136; 90
2093.91Liu, Xia; Li, Bohan; Jin, Jiance; Yang, Lin; Xia, Zhiguo; Xu, Yan
Solvent-induced structural regulation and luminescence switching of hybrid copper(I) halides for encryption and anti-counterfeiting applications.
Chemical communications (Cambridge, England), 2024, 60, 9034-9037
7133454 CIFC20 H20 Cu3 I4 PP 1 21/c 112.7409; 25.0723; 7.9544
90; 106.194; 90
2440.16Liu, Xia; Li, Bohan; Jin, Jiance; Yang, Lin; Xia, Zhiguo; Xu, Yan
Solvent-induced structural regulation and luminescence switching of hybrid copper(I) halides for encryption and anti-counterfeiting applications.
Chemical communications (Cambridge, England), 2024, 60, 9034-9037
7133455 CIFC10 H10 Cl F OP 21 21 214.9064; 9.622; 19.4077
90; 90; 90
916.23He, Bin; Chen, Gen-Qiang; Zhang, Xumu
Highly efficient synthesis of enantioenriched vicinal halohydrins <i>via</i> Ir-catalyzed asymmetric hydrogenation using dynamic kinetic resolution.
Chemical communications (Cambridge, England), 2024, 60, 9785-9788
7133456 CIFC9 H8 Cl2 O2P 1 21 18.7032; 4.8645; 11.7272
90; 110.291; 90
465.68He, Bin; Chen, Gen-Qiang; Zhang, Xumu
Highly efficient synthesis of enantioenriched vicinal halohydrins <i>via</i> Ir-catalyzed asymmetric hydrogenation using dynamic kinetic resolution.
Chemical communications (Cambridge, England), 2024, 60, 9785-9788
7133457 CIFC20 H18 N4 O2P n a 2116.083; 19.232; 5.595
90; 90; 90
1731Maiti, Sandip; Parui, Nabin; Halder, Joydev; Dash, Jyotirmayee
Synthesis of triazole-fused tetracyclic spirooxindole derivatives <i>via</i> metal-free Huisgen cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 10009-10012
7133458 CIFC17 H18 N4 OP 1 21/c 19.422; 20.895; 7.919
90; 106.63; 90
1493.8Maiti, Sandip; Parui, Nabin; Halder, Joydev; Dash, Jyotirmayee
Synthesis of triazole-fused tetracyclic spirooxindole derivatives <i>via</i> metal-free Huisgen cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 10009-10012
7133459 CIFC50 H43 Cl2 F6 Ir N4 O6 P2 Ru S2P -113.0649; 14.1192; 15.099
79.524; 69.725; 87.357
2568.7Kawaji, Kanade; Tsujiwaki, Mina; Kiso, Ayaka; Kitajo, Yukina; Kitamura, Manami; Nishimura, Minako; Horikawa, Junya; Ikushuma, Haruto; Takemoto, Shin; Matsuzaka, Hiroyuki
Bimetallic Ru-Ir/Rh complexes for catalytic allyl alcohol reduction to propylene.
Chemical communications (Cambridge, England), 2024, 60, 9424-9427
7133460 CIFC50 H45 F6 N4 O7 P2 Rh Ru S2P -112.87; 13.8567; 14.2225
99.607; 95.647; 92.404
2484.3Kawaji, Kanade; Tsujiwaki, Mina; Kiso, Ayaka; Kitajo, Yukina; Kitamura, Manami; Nishimura, Minako; Horikawa, Junya; Ikushuma, Haruto; Takemoto, Shin; Matsuzaka, Hiroyuki
Bimetallic Ru-Ir/Rh complexes for catalytic allyl alcohol reduction to propylene.
Chemical communications (Cambridge, England), 2024, 60, 9424-9427
7133461 CIFC50 H53 B2 F8 Fe Ir N4 P2P -110.3466; 13.4938; 19.4429
99.672; 102.51; 106.984
2455.5Kawaji, Kanade; Tsujiwaki, Mina; Kiso, Ayaka; Kitajo, Yukina; Kitamura, Manami; Nishimura, Minako; Horikawa, Junya; Ikushuma, Haruto; Takemoto, Shin; Matsuzaka, Hiroyuki
Bimetallic Ru-Ir/Rh complexes for catalytic allyl alcohol reduction to propylene.
Chemical communications (Cambridge, England), 2024, 60, 9424-9427
7133462 CIFC22 H29 N3 OP 1 21/n 110.2333; 10.331; 18.608
90; 91.011; 90
1966.94Maestri, Claudio; Minazzi, Paolo; Grell, Toni; Colombo, Valentina; Lattuada, Luciano; Giovenzana, Giovanni B.; Travagin, Fabio
A serendipitous one-pot synthesis of the octahydro-2<i>H</i>-pyrazino[1,2-<i>a</i>]pyrazine core.
Chemical communications (Cambridge, England), 2024, 60, 9428-9431
7133463 CIFC24 H27 N O3P 1 21 17.445; 10.9474; 11.9878
90; 97.505; 90
968.676Murmu, Ranjit; Kundu, Sourav; Majhi, Moumita; Pal, Souvik; Mondal, Abhishek; Bisai, Alakesh
Total synthesis of (+)-oridamycins A and B.
Chemical communications (Cambridge, England), 2024, 60, 9737-9740
7133464 CIFC18 H34 Al4 N2 O2P -18.359; 8.9229; 9.209
99.654; 111.823; 91.082
626.13Korona, Krzesimir; Justyniak, Iwona; Pogrebetsky, James; Lemieszka, Marta; Bernatowicz, Piotr; Pietrzykowski, Antoni; Kubas, Adam; Lewiński, Janusz
Controlled hydrolysis of AlMe<sub>3</sub> to tetramethylalumoxane and a new look at incipient adducts with water.
Chemical communications (Cambridge, England), 2024, 60, 9392-9395
7133465 CIFC22 H44 Al4 N4 O2P -18.118; 13.749; 14.0249
86.298; 77.725; 73.794
1468.79Korona, Krzesimir; Justyniak, Iwona; Pogrebetsky, James; Lemieszka, Marta; Bernatowicz, Piotr; Pietrzykowski, Antoni; Kubas, Adam; Lewiński, Janusz
Controlled hydrolysis of AlMe<sub>3</sub> to tetramethylalumoxane and a new look at incipient adducts with water.
Chemical communications (Cambridge, England), 2024, 60, 9392-9395
7133466 CIFC23 H18 F6 N3 O1.5 SF d d 213.8237; 50.84; 12.4078
90; 90; 90
8720.2Giannessi, Lisa; Longo, Matteo; Massera, Chiara; Radi, Marco
Late-stage functionalization of the 4-amino-2-pyridone chemotype using electrochemical and MCR approaches.
Chemical communications (Cambridge, England), 2024, 60, 11500-11503
7133467 CIFC48.5 H34.5 Cl7.5 F12 N6 O2 S4P -110.964; 14.7925; 19.047
79.382; 87.727; 73.299
2907.9Giannessi, Lisa; Longo, Matteo; Massera, Chiara; Radi, Marco
Late-stage functionalization of the 4-amino-2-pyridone chemotype using electrochemical and MCR approaches.
Chemical communications (Cambridge, England), 2024, 60, 11500-11503
7133468 CIFC16 H16 O4P 1 21/n 16.267; 24.5964; 8.687
90; 97.236; 90
1328.4Wittmann, Stéphane; Deschamps, Elodie; Bournaud, Chloée; Guillot, Regis; Brière, Jean-François; Vo-Thanh, Giang; Toffano, Martial
Auto tandem triple cascade organocatalysis: access to bis-lactone and butenolide derivatives.
Chemical communications (Cambridge, England), 2024, 60, 9278-9281
7133469 CIFC15 H12 F3 N O3 SP 1 21/n 15.624; 25.714; 11.107
90; 103.105; 90
1564.4Sharma, Alpa; Govande, Vijaya; Mahajan, Shivangani; Sawant, Sanghapal D.
2,3-Difunctionalization of quinones: a gold-catalyzed cascade approach for trifluoromethyl-amination or sulfoximination.
Chemical communications (Cambridge, England), 2024, 60, 9598-9601
7133470 CIFC16 H7 Cl4 O9.5 Pb2R -3 :H19.6265; 19.6265; 13.3507
90; 90; 120
4453.69Khan, Samim; Naaz, Sanobar; Ahmad, Shamim; Gomila, Rosa M.; Chanthapally, Anjana; Frontera, Antonio; Mir, Mohammad Hedayetullah
Impact of halogen⋯halogen interaction on the mechanical motion of a 3D Pb(II) coordination polymer of elusive topology.
Chemical communications (Cambridge, England), 2024, 60, 10370-10373
7133471 CIFC8 H3.6 Cl2 O4.8 PbR -3 :H19.6501; 19.6501; 13.3615
90; 90; 120
4468.02Khan, Samim; Naaz, Sanobar; Ahmad, Shamim; Gomila, Rosa M.; Chanthapally, Anjana; Frontera, Antonio; Mir, Mohammad Hedayetullah
Impact of halogen⋯halogen interaction on the mechanical motion of a 3D Pb(II) coordination polymer of elusive topology.
Chemical communications (Cambridge, England), 2024, 60, 10370-10373
7133472 CIFC8 H3.814 Cl2 O4.907 PbR -3 :H19.8059; 19.8059; 13.3701
90; 90; 120
4542.08Khan, Samim; Naaz, Sanobar; Ahmad, Shamim; Gomila, Rosa M.; Chanthapally, Anjana; Frontera, Antonio; Mir, Mohammad Hedayetullah
Impact of halogen⋯halogen interaction on the mechanical motion of a 3D Pb(II) coordination polymer of elusive topology.
Chemical communications (Cambridge, England), 2024, 60, 10370-10373
7133473 CIFC8 H24 Cl6 N2 O2 SnP 1 21 19.2612; 12.665; 9.3535
90; 114.94; 90
994.8Cai, Zhuoer; Yinan, Zhang; Chen, Jian; He, Xiaofan; Zhang, Ziyue; Hua, Xiu-Ni; Sun, Baiwang
Symmetry breaking through molecular engineering to achieve "on-off-on" nonlinear optical switch in a [SnCl<sub>6</sub>]<sup>2-</sup> framework.
Chemical communications (Cambridge, England), 2024, 60, 9412-9415
7133474 CIFC8 H24 Cl6 N2 SnF m -3 m13.017; 13.017; 13.017
90; 90; 90
2205.6Cai, Zhuoer; Yinan, Zhang; Chen, Jian; He, Xiaofan; Zhang, Ziyue; Hua, Xiu-Ni; Sun, Baiwang
Symmetry breaking through molecular engineering to achieve "on-off-on" nonlinear optical switch in a [SnCl<sub>6</sub>]<sup>2-</sup> framework.
Chemical communications (Cambridge, England), 2024, 60, 9412-9415
7133475 CIFC8 H24 Cl6 N2 O2 SnP 63 m c9.6998; 9.6998; 12.6019
90; 90; 120
1026.8Cai, Zhuoer; Yinan, Zhang; Chen, Jian; He, Xiaofan; Zhang, Ziyue; Hua, Xiu-Ni; Sun, Baiwang
Symmetry breaking through molecular engineering to achieve "on-off-on" nonlinear optical switch in a [SnCl<sub>6</sub>]<sup>2-</sup> framework.
Chemical communications (Cambridge, England), 2024, 60, 9412-9415
7133476 CIFC8 H24 Cl6 N2 O2 SnC m c e14.3092; 10.9809; 13.651
90; 90; 90
2145Cai, Zhuoer; Yinan, Zhang; Chen, Jian; He, Xiaofan; Zhang, Ziyue; Hua, Xiu-Ni; Sun, Baiwang
Symmetry breaking through molecular engineering to achieve "on-off-on" nonlinear optical switch in a [SnCl<sub>6</sub>]<sup>2-</sup> framework.
Chemical communications (Cambridge, England), 2024, 60, 9412-9415
7133477 CIFC8 H24 Cl6 N2 SnF d -3 c :225.724; 25.724; 25.724
90; 90; 90
17022Cai, Zhuoer; Yinan, Zhang; Chen, Jian; He, Xiaofan; Zhang, Ziyue; Hua, Xiu-Ni; Sun, Baiwang
Symmetry breaking through molecular engineering to achieve "on-off-on" nonlinear optical switch in a [SnCl<sub>6</sub>]<sup>2-</sup> framework.
Chemical communications (Cambridge, England), 2024, 60, 9412-9415
7133478 CIFC28 H34 Co K N5 OP -110.153; 11.686; 13.651
89.533; 73.197; 64.696
1389.2Anferov, Sophie W.; Krupinski, Alexandra; Anderson, John S.
Synthesis of a potassium capped terminal cobalt-oxido complex.
Chemical communications (Cambridge, England), 2024, 60, 9562-9565
7133479 CIFC30 H37 Co N6P 21 21 218.9652; 11.2879; 27.8086
90; 90; 90
2814.2Anferov, Sophie W.; Krupinski, Alexandra; Anderson, John S.
Synthesis of a potassium capped terminal cobalt-oxido complex.
Chemical communications (Cambridge, England), 2024, 60, 9562-9565
7133480 CIFC31 H22 N4 O2C 1 2/c 118.947; 16.244; 15.993
90; 104.238; 90
4771Shen, Xi; Yu, Zhi-Cheng; Zhou, You; Wu, Yan-Dong; Wu, An-Xin
Divergent synthesis of pyrrolidone fused pyrimido[1,2-<i>b</i>]indazole through selective trapping of an enone intermediate by 1<i>H</i>-indazol-3-amine.
Chemical communications (Cambridge, England), 2024, 60, 9781-9784
7133481 CIFC32 H26 F N4 O3 SP 1 21/n 112.761; 11.663; 19.57
90; 107.371; 90
2779.8Shen, Xi; Yu, Zhi-Cheng; Zhou, You; Wu, Yan-Dong; Wu, An-Xin
Divergent synthesis of pyrrolidone fused pyrimido[1,2-<i>b</i>]indazole through selective trapping of an enone intermediate by 1<i>H</i>-indazol-3-amine.
Chemical communications (Cambridge, England), 2024, 60, 9781-9784
7133482 CIFC13 H15 N O4P 1 21 17.5054; 10.0086; 8.5104
90; 110.518; 90
598.73Tian, Jin-Rui; Qiao, Yu-Hao; Zhuang, Qing-Bo; Fan, Rong; Li, Zhen; Zhang, Xiao-Ming; Zhang, Fu-Min; Tu, Yong-Qiang
Organo-cation catalyzed enantioselective α-hydroxylation of pyridinone-fused lactones: asymmetric synthesis of SN-38 and irinotecan.
Chemical communications (Cambridge, England), 2024, 60, 9954-9957
7133483 CIFC41 H34 Cl2 I N2 O2C 1 2 126.7116; 10.1135; 16.0912
90; 122.776; 90
3654.9Rui, Kanghua; Huang, Shaoying; Wu, Yinong; Shen, Hanxiao; Lin, Xufeng
Organocatalytic enantioselective (4+3) cyclization for the synthesis of spiro-fused heterocyclic compounds containing isoindolinone, oxepine and indole moieties.
Chemical communications (Cambridge, England), 2024, 60, 9400-9403
7133484 CIFC13 H16 F3 N O3 SP -17.1898; 10.261; 10.7376
82.873; 81.112; 73.186
746.55Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133485 CIFC15 H20 B F4 NP 1 21/c 110.0997; 8.3125; 17.8495
90; 96.121; 90
1489.99Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133486 CIFC14 H18 B F4 NP 1 21/n 18.57365; 16.306; 9.96321
90; 90.6392; 90
1392.79Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133487 CIFC14 H17 B F5 NP 1 21/n 18.51495; 16.4158; 10.0399
90; 90.742; 90
1403.26Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133488 CIFC15 H20 B F4 N OP 1 21/n 17.63744; 19.68; 10.11448
90; 100.728; 90
1493.68Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133489 CIFC15 H20 B F4 NP 1 21/n 17.5602; 15.2074; 12.6685
90; 95.164; 90
1450.6Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133490 CIFC15 H20 B F4 NP 1 21/c 110.11; 8.7342; 16.7607
90; 90.82; 90
1479.86Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133491 CIFC17 H24 B F4 N O3P -17.6902; 9.9674; 12.0352
94.287; 96.2441; 96.7987
907Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133492 CIFC28 H36 B2 F8 N2P 1 21 17.1302; 14.6918; 13.1044
90; 101.392; 90
1345.71Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133493 CIFC26 H26 O2P 1 21 19.0741; 13.3976; 9.2157
90; 115.37; 90
1012.32Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133494 CIFC28 H36 F2 N2P 1 21 19.36553; 10.40596; 12.2778
90; 99.9106; 90
1178.71Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133495 CIFC20 H22 F2 O2P 1 2/c 115.5432; 10.8346; 20.429
90; 98.712; 90
3400.64Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133496 CIFC20 H20 O2P 1 21/n 19.64367; 16.3794; 11.2234
90; 115.752; 90
1596.75Yamada, Shinji; Honda, Yuka
Solid-state [2+2] photodimerization of eniminium salts: stereoselective syntheses of 1,3-diacetylcyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 9821-9824
7133497 CIFC42 H24 O13 Zn4F m -3 m34.3966; 34.3966; 34.3966
90; 90; 90
40695.5Carey, Cassidy A.; Foroughi, Leila M.; Matzger, Adam J.
Designed additive suppresses interpenetration in IRMOF-10.
Chemical communications (Cambridge, England), 2024, 60, 9396-9399
7133498 CIFC68 H3 F3 OP 1 2/c 117.3452; 10.073; 19.9427
90; 90.496; 90
3484.2Zhai, Yong-Chang; Yamanaka, Koki; Yu, Chu-Yang; Wang, Jun-Zhuo; Zheng, Xue-Lin; Huda, Miftakhul; Imai, Naoyuki; Igarashi, Takeshi; Aoyagi, Shinobu; Matsuo, Yutaka
Hydrophobic evaporable fullerene indanone ketone with low sublimation temperature and amorphous morphology for inverted perovskite solar cells.
Chemical communications (Cambridge, England), 2024, 60, 9420-9423
7133499 CIFC32 H28 N2 OP 1 21/n 121.5474; 11.3765; 22.1803
90; 113.87; 90
4972.1Nian, Cuicui; Yu, Run; Han, Zhengyu; Bai, Yang; Wang, Jianhao; Sun, Jianwei; Huang, Hai
Trifluoroethanol promoted formal nucleophilic substitution of indol-2-yl diaryl methanol for the synthesis of tetraarylmethanes.
Chemical communications (Cambridge, England), 2024, 60, 9797-9800
7133500 CIFC45 H53 N2 P SnP 1 21/c 110.1795; 10.3793; 38.58
90; 91.604; 90
4074.6Wei, Rui; Wang, Xin-Feng; Hu, Chaopeng; Liu, Liu Leo
(Phosphino)(stannyl)carbene.
Chemical communications (Cambridge, England), 2024, 60, 9793-9796
7133501 CIFC45 H53 N4 P SnP -19.9707; 10.4091; 20.4298
89.295; 76.839; 77.221
2011.88Wei, Rui; Wang, Xin-Feng; Hu, Chaopeng; Liu, Liu Leo
(Phosphino)(stannyl)carbene.
Chemical communications (Cambridge, England), 2024, 60, 9793-9796
7133502 CIFC49 H62 N3 P Si SnP 1 21/c 118.0214; 12.3053; 20.7838
90; 93.773; 90
4599Wei, Rui; Wang, Xin-Feng; Hu, Chaopeng; Liu, Liu Leo
(Phosphino)(stannyl)carbene.
Chemical communications (Cambridge, England), 2024, 60, 9793-9796
7133503 CIFC46 H53 N2 O P SnP -19.9668; 10.3764; 20.4573
89.474; 76.827; 77.353
2008.18Wei, Rui; Wang, Xin-Feng; Hu, Chaopeng; Liu, Liu Leo
(Phosphino)(stannyl)carbene.
Chemical communications (Cambridge, England), 2024, 60, 9793-9796
7133504 CIFC54 H62 N3 P SnP 1 21/c 120.5741; 18.2905; 12.3909
90; 90.541; 90
4662.62Wei, Rui; Wang, Xin-Feng; Hu, Chaopeng; Liu, Liu Leo
(Phosphino)(stannyl)carbene.
Chemical communications (Cambridge, England), 2024, 60, 9793-9796
7133505 CIFC90 H93 Cl4 Co2 F12 N20 O0.5 P2P -112.0852; 17.3585; 22.5821
70.146; 79.514; 85.984
4381.1Bhandari, Anirban; Park, Gyeong Min; Lee, Heui Beom; Hong, Sugyeong; Kim, Sun Hee; Byon, Hye Ryung; Lee, Yunho
A stable radical within a N-Co-N core.
Chemical communications (Cambridge, England), 2024, 60, 9970-9973
7133506 CIFC44 H44 Co I6 N10P -111.0762; 11.838; 18.9588
93.125; 95.401; 90.195
2471.1Bhandari, Anirban; Park, Gyeong Min; Lee, Heui Beom; Hong, Sugyeong; Kim, Sun Hee; Byon, Hye Ryung; Lee, Yunho
A stable radical within a N-Co-N core.
Chemical communications (Cambridge, England), 2024, 60, 9970-9973
7133507 CIFC46 H47 Co F12 N11 P2R 3 c :H41.229; 41.229; 20.2204
90; 90; 120
29766Bhandari, Anirban; Park, Gyeong Min; Lee, Heui Beom; Hong, Sugyeong; Kim, Sun Hee; Byon, Hye Ryung; Lee, Yunho
A stable radical within a N-Co-N core.
Chemical communications (Cambridge, England), 2024, 60, 9970-9973
7133508 CIFC20 H24 Ce Cl8 N4P -17.5899; 9.2556; 11.8931
100.578; 104.99; 107.349
738.9Blanes-Díaz, Anamar; Wacker, Jennifer N.; Szymanowski, Jennifer E. S.; Bertke, Jeffery A.; Knope, Karah E.
Isolation of a chloride-capped cerium polyoxo nanocluster built from 52 metal ions.
Chemical communications (Cambridge, England), 2024, 60, 12185-12188
7133509 CIFC10 H12 Ce Cl6 N2C 1 2/m 112.993; 8.6538; 7.9621
90; 97.827; 90
886.91Blanes-Díaz, Anamar; Wacker, Jennifer N.; Szymanowski, Jennifer E. S.; Bertke, Jeffery A.; Knope, Karah E.
Isolation of a chloride-capped cerium polyoxo nanocluster built from 52 metal ions.
Chemical communications (Cambridge, England), 2024, 60, 12185-12188
7133510 CIFC20 H24 Ce38 Cl50 N4 O92P 1 21/n 118.8106; 18.7789; 28.4413
90; 97.602; 90
9958.4Blanes-Díaz, Anamar; Wacker, Jennifer N.; Szymanowski, Jennifer E. S.; Bertke, Jeffery A.; Knope, Karah E.
Isolation of a chloride-capped cerium polyoxo nanocluster built from 52 metal ions.
Chemical communications (Cambridge, England), 2024, 60, 12185-12188
7133511 CIFC0 H0 Ce104 Cl118 N0 O194P 1 2/m 122.2147; 29.7354; 24.3598
90; 102.365; 90
15717.9Blanes-Díaz, Anamar; Wacker, Jennifer N.; Szymanowski, Jennifer E. S.; Bertke, Jeffery A.; Knope, Karah E.
Isolation of a chloride-capped cerium polyoxo nanocluster built from 52 metal ions.
Chemical communications (Cambridge, England), 2024, 60, 12185-12188
7133512 CIFC34 H64 Ge N2 O5 Si4P -19.5714; 13.252; 17.5019
97.149; 97.276; 102.064
2127.2Ajithkumar, V. S.; Ghanwat, Pratiksha B.; Saha, Sougata; Pati, Swapan K.; Sen, Sakya S.
Stereodivergent sila-germylenation <i>vs.</i> sila-stannylenation of an internal alkyne.
Chemical communications (Cambridge, England), 2024, 60, 9837-9840
7133513 CIFC30 H56 N2 O4 Si4 SnP 1 21/n 110.2751; 15.191; 25.182
90; 99.29; 90
3879.1Ajithkumar, V. S.; Ghanwat, Pratiksha B.; Saha, Sougata; Pati, Swapan K.; Sen, Sakya S.
Stereodivergent sila-germylenation <i>vs.</i> sila-stannylenation of an internal alkyne.
Chemical communications (Cambridge, England), 2024, 60, 9837-9840
7133514 CIFC80 H104 Na2 O6 Si2P -17.7756; 14.1848; 16.3912
97.316; 100.192; 100.448
1725.94Pennachio, Matthew; Wei, Zheng; Mamada, Masashi; Frigoli, Michel; Petrukhina, Marina A.
Chemical reduction of π-expanded functionalized pentacene: cooperation of side group in alkali metal binding.
Chemical communications (Cambridge, England), 2024, 60, 9526-9529
7133515 CIFC28 H24 Cu F12 N6 O8 S4C 1 2 119.966; 9.159; 11.301
90; 108.602; 90
1958.6Ohara, Yuki; Nishiguchi, Taichi; Zheng, Xin; Noro, Shin-Ichiro; Packwood, Daniel M.; Horike, Satoshi
Entropically driven melting of Cu-based 1D coordination polymers.
Chemical communications (Cambridge, England), 2024, 60, 9833-9836
7133516 CIFC33 H54 N3 P SiP -110.461; 10.611; 16.467
83.31; 87.04; 67.44
1676Kaulage, Sandeep H.; Parvin, Nasrina; Khopade, Kishor V.; Khan, Shabana
A hybrid silylene-Pd catalyst: efficient C-N cross-coupling of sterically bulky amines and chiral amines.
Chemical communications (Cambridge, England), 2024, 60, 9958-9961
7133517 CIFC46 H47 NP 1 21/n 112.506; 23.229; 13.297
90; 114.039; 90
3528Kaulage, Sandeep H.; Parvin, Nasrina; Khopade, Kishor V.; Khan, Shabana
A hybrid silylene-Pd catalyst: efficient C-N cross-coupling of sterically bulky amines and chiral amines.
Chemical communications (Cambridge, England), 2024, 60, 9958-9961

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