Crystallography Open Database

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7131524 CIFC46 H106 Al2 N Nd O6 Si2P 1 21/c 114.132; 15.5704; 26.282
90; 91.616; 90
5780.8Moinet, Eric C.; Tardif, Olivier; Maichle-Mössmer, Cäcilia; Anwander, Reiner
Triisobutylaluminium-promoted formation of lanthanide hydrides.
Chemical communications (Cambridge, England), 2023, 59, 5261-5264
7131525 CIFC34 H82 Al2 N Pr Si2P -19.309; 11.5249; 21.018
94.562; 101.615; 92.784
2196.9Moinet, Eric C.; Tardif, Olivier; Maichle-Mössmer, Cäcilia; Anwander, Reiner
Triisobutylaluminium-promoted formation of lanthanide hydrides.
Chemical communications (Cambridge, England), 2023, 59, 5261-5264
7131526 CIFC6 H9 N8 O3 Zn2P n m a9.711; 16.129; 9.7091
90; 90; 90
1520.7Singh, Piyush; Singh, Himan Dev; Menon, Abhijith Hari; Vaidhyanathan, Ramanathan
Preferential CO<sub>2</sub> adsorption by an ultra-microporous zinc-aminotriazolato-acetate MOF.
Chemical communications (Cambridge, England), 2023, 59, 5559-5562
7131527 CIFC42 H76 Al I N2 Si2P 1 21/c 118.8006; 13.66544; 18.6649
90; 112.8; 90
4420.66Jackson, Ross A.; Matthews, Aidan J. R.; Vasko, Petra; Mahon, Mary F.; Hicks, Jamie; Liptrot, David J.
An acyclic aluminyl anion.
Chemical communications (Cambridge, England), 2023, 59, 5277-5280
7131528 CIFC30 H52 Al I N2 Si2P -110.1072; 10.2573; 17.9608
89.292; 83.539; 66.374
1694.04Jackson, Ross A.; Matthews, Aidan J. R.; Vasko, Petra; Mahon, Mary F.; Hicks, Jamie; Liptrot, David J.
An acyclic aluminyl anion.
Chemical communications (Cambridge, England), 2023, 59, 5277-5280
7131529 CIFC66 H101 Al Mg N4 Si2P -112.8772; 14.6377; 17.2412
87.531; 83.372; 84.087
3209.3Jackson, Ross A.; Matthews, Aidan J. R.; Vasko, Petra; Mahon, Mary F.; Hicks, Jamie; Liptrot, David J.
An acyclic aluminyl anion.
Chemical communications (Cambridge, England), 2023, 59, 5277-5280
7131530 CIFC42 H76 Al K N2 Si2P 21 21 2113.19442; 14.99103; 22.2823
90; 90; 90
4407.39Jackson, Ross A.; Matthews, Aidan J. R.; Vasko, Petra; Mahon, Mary F.; Hicks, Jamie; Liptrot, David J.
An acyclic aluminyl anion.
Chemical communications (Cambridge, England), 2023, 59, 5277-5280
7131531 CIFC36 H58 Al K N2 Si2P 21 21 222.1102; 33.7684; 10.73
90; 90; 90
8011.3Jackson, Ross A.; Matthews, Aidan J. R.; Vasko, Petra; Mahon, Mary F.; Hicks, Jamie; Liptrot, David J.
An acyclic aluminyl anion.
Chemical communications (Cambridge, England), 2023, 59, 5277-5280
7131532 CIFC190 H296 Cl4 Eu26 F18 N4 O204 S2 Zn22P -119.8012; 22.2405; 25.7774
85.187; 85.307; 72.362
10761.2Zhao, Jinni; Leng, Xilong; Lin, Jiazhao; Yang, Xiaoping; Lv, Xiaoli; Huang, Xianfeng; Yang, Zhi; Schipper, Desmond
Rapid and quantitative detection of the inflammatory marker neopterin based on a visible luminescent Zn(II)-Eu(III) nanocluster.
Chemical communications (Cambridge, England), 2023, 59, 5435-5438
7131533 CIFC72 H60 Br4 I4 N4 O16P 21 21 219.8468; 10.3709; 17.4196
90; 90; 90
1778.89Dutta, Sourav; Porey, Arka; Guin, Joyram
N-Heterocyclic carbene catalyzed desymmetrization of diols: access to enantioenriched oxindoles having a C3-quaternary stereocenter.
Chemical communications (Cambridge, England), 2023, 59, 5771-5774
7131534 CIFC65 H61 B Cl3 N3P 1 21/n 115.1246; 15.3418; 23.6578
90; 99.404; 90
5415.7Xiao, Xin; Lei, Bowen; Wu, Di; Bin, Zhengyang
"Medium-ring" strategy enables high-performance narrowband pure-blue multi-resonance emitters: boost provided by a unique perpendicular geometry.
Chemical communications (Cambridge, England), 2023, 59, 6556-6559
7131535 CIFC26 H55 Co F2 N2 Na O2 Si4P 1 21/n 117.5676; 11.28947; 20.1652
90; 112.362; 90
3698.58Logallo, Alessandra; Hevia, Eva
Applying Na/Co(II) bimetallic partnerships to promote multiple Co-H exchanges in polyfluoroarenes.
Chemical communications (Cambridge, England), 2023, 59, 5383-5386
7131536 CIFC60 H146 Co4 F6 N8 Na4 Si16P -19.8682; 16.3345; 18.12805
113.061; 102.112; 98.0739
2546.96Logallo, Alessandra; Hevia, Eva
Applying Na/Co(II) bimetallic partnerships to promote multiple Co-H exchanges in polyfluoroarenes.
Chemical communications (Cambridge, England), 2023, 59, 5383-5386
7131537 CIFC36 H91 Co2 N5 Si10P 1 21 19.10611; 29.0863; 32.9649
90; 95.7961; 90
8686.55Logallo, Alessandra; Hevia, Eva
Applying Na/Co(II) bimetallic partnerships to promote multiple Co-H exchanges in polyfluoroarenes.
Chemical communications (Cambridge, England), 2023, 59, 5383-5386
7131538 CIFC18 H38 Co F3 Li N2 Si4C c c 213.3832; 18.7778; 10.86351
90; 90; 90
2730.08Logallo, Alessandra; Hevia, Eva
Applying Na/Co(II) bimetallic partnerships to promote multiple Co-H exchanges in polyfluoroarenes.
Chemical communications (Cambridge, England), 2023, 59, 5383-5386
7131539 CIFC138 H276 Co8 F20 N14 Na8 Si28P 1 21/c 121.6543; 17.95986; 27.5932
90; 97.4528; 90
10640.6Logallo, Alessandra; Hevia, Eva
Applying Na/Co(II) bimetallic partnerships to promote multiple Co-H exchanges in polyfluoroarenes.
Chemical communications (Cambridge, England), 2023, 59, 5383-5386
7131540 CIFC416.5 H560.5 Cl6 Co24 N45.5 Na4 O117.5 S24I 4/m25.716; 25.716; 43.4014
90; 90; 90
28702Guo, Yinjuan; Li, Jiahui; Zhao, Guiyan; Chen, Baokuan; Hang, Xinxin; Bi, Yanfeng
Post-synthetic atomically precise single-Cu<sup>II</sup> sites in a thiacalix[4]arene-supported octahedral Na@Co<sub>24</sub> cluster: the Cu-Co synergistic effect for selective photocatalytic conversion of CO<sub>2</sub> to CO.
Chemical communications (Cambridge, England), 2023, 59, 5591-5594
7131541 CIFC334.5 H337 Cl82.5 Co24 Cu2.5 N8 Na O84.5 S24I 4/m25.981; 25.981; 43.544
90; 90; 90
29393Guo, Yinjuan; Li, Jiahui; Zhao, Guiyan; Chen, Baokuan; Hang, Xinxin; Bi, Yanfeng
Post-synthetic atomically precise single-Cu<sup>II</sup> sites in a thiacalix[4]arene-supported octahedral Na@Co<sub>24</sub> cluster: the Cu-Co synergistic effect for selective photocatalytic conversion of CO<sub>2</sub> to CO.
Chemical communications (Cambridge, England), 2023, 59, 5591-5594
7131542 CIFC33 H22 Br N O6C 2 2 2112.3684; 14.0492; 60.098
90; 90; 90
10443Inoue, Ryo; Furumoto, Kyosuke; Morisaki, Yasuhiro
Syntheses of heterotriptycenes and their Pt complexes that emit circularly polarised fluorescence and phosphorescence.
Chemical communications (Cambridge, England), 2023, 59, 5571-5574
7131543 CIFC29 H21 Br F N O4C 2 2 2112.0615; 14.387; 61.506
90; 90; 90
10673.1Inoue, Ryo; Furumoto, Kyosuke; Morisaki, Yasuhiro
Syntheses of heterotriptycenes and their Pt complexes that emit circularly polarised fluorescence and phosphorescence.
Chemical communications (Cambridge, England), 2023, 59, 5571-5574
7131544 CIFC22 H26 O4 SP 1 21/c 119.4337; 6.5348; 17.2542
90; 114.748; 90
1989.96Halder, Indranil; Nair, Akshay M.; Volla, Chandra M. R.
A visible light mediated alkyl sulfonylative cascade using Hantzsch esters <i>via</i> SO<sub>2</sub> insertion.
Chemical communications (Cambridge, England), 2023, 59, 5862-5865
7131545 CIFC22 H28 O4 SP 21 21 2110.5572; 12.2026; 15.4049
90; 90; 90
1984.54Halder, Indranil; Nair, Akshay M.; Volla, Chandra M. R.
A visible light mediated alkyl sulfonylative cascade using Hantzsch esters <i>via</i> SO<sub>2</sub> insertion.
Chemical communications (Cambridge, England), 2023, 59, 5862-5865
7131546 CIFC31 H32 O4P b c a12.88; 18.325; 21.134
90; 90; 90
4988Saravanan, Velautham; Jeganmohan, Masilamani
Palladium-catalyzed stereocontrolled ring-opening of 7-oxabenzonorbornadienes with organic carboxylic acids.
Chemical communications (Cambridge, England), 2023, 59, 5619-5622
7131547 CIFC47 H40 F12 N6 O9 P2 S4 ZnP -112.6499; 14.203; 16.8
77.885; 75.56; 77.008
2810.1Eltester, M. Alexander; Gildenast, Hans; Rabatinová, Kristína; Pütz, Christopher; Cremer, Christopher; Lanzerath, Patrick; Schroers, Julian P.; Tauchert, Michael E.
Au → M bonds promote catalytic alkyne hydrofunctionalisation.
Chemical communications (Cambridge, England), 2023, 59, 5459-5462
7131548 CIFC46 H44 Au Br F12 N4 O P2 Sb2 ZnP n m a34.469; 13.371; 11.347
90; 90; 90
5229.7Eltester, M. Alexander; Gildenast, Hans; Rabatinová, Kristína; Pütz, Christopher; Cremer, Christopher; Lanzerath, Patrick; Schroers, Julian P.; Tauchert, Michael E.
Au → M bonds promote catalytic alkyne hydrofunctionalisation.
Chemical communications (Cambridge, England), 2023, 59, 5459-5462
7131549 CIFC47 H44 Au Cl Cu F3 N4 O4 P2 SP n m a27.215; 15.3259; 11.2478
90; 90; 90
4691.4Eltester, M. Alexander; Gildenast, Hans; Rabatinová, Kristína; Pütz, Christopher; Cremer, Christopher; Lanzerath, Patrick; Schroers, Julian P.; Tauchert, Michael E.
Au → M bonds promote catalytic alkyne hydrofunctionalisation.
Chemical communications (Cambridge, England), 2023, 59, 5459-5462
7131550 CIFC54 H52 Au Cl F12 N6 O10 P2 S4 ZnP n m a11.1687; 16.198; 34.695
90; 90; 90
6276.7Eltester, M. Alexander; Gildenast, Hans; Rabatinová, Kristína; Pütz, Christopher; Cremer, Christopher; Lanzerath, Patrick; Schroers, Julian P.; Tauchert, Michael E.
Au → M bonds promote catalytic alkyne hydrofunctionalisation.
Chemical communications (Cambridge, England), 2023, 59, 5459-5462
7131551 CIFC52 H52 Ag Au F12 N6 O8 P2 S5P -114.1986; 15.7612; 15.7808
96.576; 108.838; 107.971
3088.1Eltester, M. Alexander; Gildenast, Hans; Rabatinová, Kristína; Pütz, Christopher; Cremer, Christopher; Lanzerath, Patrick; Schroers, Julian P.; Tauchert, Michael E.
Au → M bonds promote catalytic alkyne hydrofunctionalisation.
Chemical communications (Cambridge, England), 2023, 59, 5459-5462
7131552 CIFC55 H45 Ag Au F12 N6 O8 P2 S4P b c a16.5099; 26.641; 27.507
90; 90; 90
12099Eltester, M. Alexander; Gildenast, Hans; Rabatinová, Kristína; Pütz, Christopher; Cremer, Christopher; Lanzerath, Patrick; Schroers, Julian P.; Tauchert, Michael E.
Au → M bonds promote catalytic alkyne hydrofunctionalisation.
Chemical communications (Cambridge, England), 2023, 59, 5459-5462
7131553 CIFC49 H38 Au Cl2 F18 N7 O12 P2 S6 ZnP 1 21 114.81742; 17.256; 25.0836
90; 95.1264; 90
6387.96Eltester, M. Alexander; Gildenast, Hans; Rabatinová, Kristína; Pütz, Christopher; Cremer, Christopher; Lanzerath, Patrick; Schroers, Julian P.; Tauchert, Michael E.
Au → M bonds promote catalytic alkyne hydrofunctionalisation.
Chemical communications (Cambridge, England), 2023, 59, 5459-5462
7131554 CIFC18 H14 N2P 1 21/n 16.5843; 9.6121; 20.5866
90; 93.744; 90
1300.12Begam, Hasina Mamataj; Pradhan, Kangkan; Varalaxmi, Kasarla; Jana, Ranjan
An HFIP-assisted, cobalt-catalyzed three-component electrophilic C-H amination/cyclization/directing group removal cascade to naphtho[1,2-d]imidazoles.
Chemical communications (Cambridge, England), 2023, 59, 5595-5598
7131555 CIFC17 H18 N2P 1 21/c 113.2417; 12.7619; 7.809
90; 99.428; 90
1301.81Begam, Hasina Mamataj; Pradhan, Kangkan; Varalaxmi, Kasarla; Jana, Ranjan
An HFIP-assisted, cobalt-catalyzed three-component electrophilic C-H amination/cyclization/directing group removal cascade to naphtho[1,2-d]imidazoles.
Chemical communications (Cambridge, England), 2023, 59, 5595-5598
7131556 CIFC38 H14 F10 N4P 1 21/a 17.5781; 25.7071; 14.971
90; 104.588; 90
2822.49Kielesiński, Łukasz; Summa, Francesco F.; Conradie, Jeanet; Honig, Hilah C.; Friedman, Ariel; Monaco, Gugliemo; Elbaz, Lior; Ghosh, Abhik; Gryko, Daniel T.
Nonaromatic naphthocorroles.
Chemical communications (Cambridge, England), 2023, 59, 5439-5442
7131557 CIFC57 H61 B Cl F6 O1.75 P5 PtP b c n23.859; 23.456; 20.743
90; 90; 90
11609Wehmeyer, Frerk-Ulfert; Langer, Robert
A hampered oxidative addition of pre-coordinated pincer ligands can favour alternative pathways of activation.
Chemical communications (Cambridge, England), 2023, 59, 6004-6007
7131558 CIFC53.5 H50 B F6 P5 PtP 1 21/n 111.728; 26.813; 17.242
90; 102.88; 90
5285.5Wehmeyer, Frerk-Ulfert; Langer, Robert
A hampered oxidative addition of pre-coordinated pincer ligands can favour alternative pathways of activation.
Chemical communications (Cambridge, England), 2023, 59, 6004-6007
7131559 CIFC28 H20 Br Cl2 N2 O3P 21 21 219.824; 14.724; 17.133
90; 90; 90
2478Ji, Hong; Zou, Juan; Mou, Chengli; Liu, Yonggui; Ren, Shi-Chao; Chi, Yonggui Robin
NHC-catalyzed [12+2] reaction of polycyclic arylaldehydes for access to indole derivatives.
Chemical communications (Cambridge, England), 2023, 59, 6351-6354
7131560 CIFC13 H15 N O5P 1 21/n 16.2791; 26.416; 8.3767
90; 109.284; 90
1311.48Thai-Savard, Léa; Charette, André B
Synthesis of 2-substituted bicyclo[1.1.0]butanes <i>via</i> zincocyclopropanation using bromoform as the carbenoid precursor.
Chemical communications (Cambridge, England), 2023, 59, 5273-5276
7131561 CIFC21 H23 N3 O2P 1 21/n 115.3404; 5.5177; 21.3195
90; 97.548; 90
1788.93Thai-Savard, Léa; Charette, André B
Synthesis of 2-substituted bicyclo[1.1.0]butanes <i>via</i> zincocyclopropanation using bromoform as the carbenoid precursor.
Chemical communications (Cambridge, England), 2023, 59, 5273-5276
7131562 CIFC30 H28 N2 O8C 2 2 217.9768; 29.4996; 23.6631
90; 90; 90
5568.2Oketani, Ryusei; Shiohara, Koki; Hisaki, Ichiro
Overcoming a solid solution system on chiral resolution: combining crystallization and enantioselective dissolution.
Chemical communications (Cambridge, England), 2023, 59, 6175-6178
7131563 CIFC12 H36 As6 Au3 Cl N Na3 O27 Pt2P 63/m10.9156; 10.9156; 26.8948
90; 90; 120
2775.2Zhang, Jiayao; Bhattacharya, Saurav; Müller, Anja B; Kiss, Levente; Silvestru, Cristian; Kuhnert, Nikolai; Kortz, Ulrich
Mixed noble metal-oxo clusters: platinum(IV)-gold(III) oxoanion [Pt<sup>IV</sup><sub>2</sub>Au<sup>III</sup><sub>3</sub>O<sub>6</sub>((CH<sub>3</sub>)<sub>2</sub>AsO<sub>2</sub>)<sub>6</sub>]<sup/>.
Chemical communications (Cambridge, England), 2023, 59, 5918-5921
7131564 CIFC12 H36 As6 Au3 Cl N Na3 O27 Pt2P -610.933; 10.933; 20.585
90; 90; 120
2130.9Zhang, Jiayao; Bhattacharya, Saurav; Müller, Anja B; Kiss, Levente; Silvestru, Cristian; Kuhnert, Nikolai; Kortz, Ulrich
Mixed noble metal-oxo clusters: platinum(IV)-gold(III) oxoanion [Pt<sup>IV</sup><sub>2</sub>Au<sup>III</sup><sub>3</sub>O<sub>6</sub>((CH<sub>3</sub>)<sub>2</sub>AsO<sub>2</sub>)<sub>6</sub>]<sup/>.
Chemical communications (Cambridge, England), 2023, 59, 5918-5921
7131565 CIFC14 H64 As7 Au3 Cl K3 O31 Pt2P -113.5559; 14.1105; 16.6726
75.614; 66.913; 85.534
2841.1Zhang, Jiayao; Bhattacharya, Saurav; Müller, Anja B; Kiss, Levente; Silvestru, Cristian; Kuhnert, Nikolai; Kortz, Ulrich
Mixed noble metal-oxo clusters: platinum(IV)-gold(III) oxoanion [Pt<sup>IV</sup><sub>2</sub>Au<sup>III</sup><sub>3</sub>O<sub>6</sub>((CH<sub>3</sub>)<sub>2</sub>AsO<sub>2</sub>)<sub>6</sub>]<sup/>.
Chemical communications (Cambridge, England), 2023, 59, 5918-5921
7131566 CIFC17 H22 N2 O3P 1 21/c 112.1041; 11.5162; 10.8177
90; 95.407; 90
1501.2Hindle, Alexandra; Baj, Krzysztof; Iggo, Jonathan A.; Cox, Daniel J.; Pask, Christopher M.; Nelson, Adam; Marsden, Stephen P.
Modular synthesis of bicyclic twisted amides and anilines.
Chemical communications (Cambridge, England), 2023, 59, 6239-6242
7131567 CIFC52 H70 N18 O26 ZnP 1 21/c 115.936; 18.3877; 21.801
90; 104.97; 90
6171.5Wu, Weijie; Xu, Yinghao; Wang, Shoujun; Pang, Qingqing; Liu, Simin
Metal-organic rotaxane frameworks constructed from a cucurbit[8]uril-based ternary complex for the selective detection of antibiotics.
Chemical communications (Cambridge, England), 2023, 59, 5890-5893
7131568 CIFC51 H90 Cd N18 O37P -115.0854; 15.8414; 16.6026
77.578; 73.354; 78.418
3671Wu, Weijie; Xu, Yinghao; Wang, Shoujun; Pang, Qingqing; Liu, Simin
Metal-organic rotaxane frameworks constructed from a cucurbit[8]uril-based ternary complex for the selective detection of antibiotics.
Chemical communications (Cambridge, England), 2023, 59, 5890-5893
7131569 CIFC34 H22 Cl N O2P -18.8279; 11.8609; 13.5405
68.435; 73.562; 72.877
1235.5Naskar, Koushik; Karmakar, Sudip; Mondal, Imtiaj; Sarkar, Writhabrata; Roy, Shantonu; Roy, Anupam; Deb, Indubhusan
Synthesis of indene-fused spiro-dibenz(ox)azepines <i>via</i> Rh(III)-catalyzed cascade regioselective C-H activation/annulation.
Chemical communications (Cambridge, England), 2023, 59, 7751-7754
7131570 CIFC35 H25 N OP 21 21 219.8267; 9.9692; 24.995
90; 90; 90
2448.6Naskar, Koushik; Karmakar, Sudip; Mondal, Imtiaj; Sarkar, Writhabrata; Roy, Shantonu; Roy, Anupam; Deb, Indubhusan
Synthesis of indene-fused spiro-dibenz(ox)azepines <i>via</i> Rh(III)-catalyzed cascade regioselective C-H activation/annulation.
Chemical communications (Cambridge, England), 2023, 59, 7751-7754
7131571 CIFC36 H25 N O2P -110.6943; 11.3031; 12.5505
70.572; 89.851; 66.309
1294.96Naskar, Koushik; Karmakar, Sudip; Mondal, Imtiaj; Sarkar, Writhabrata; Roy, Shantonu; Roy, Anupam; Deb, Indubhusan
Synthesis of indene-fused spiro-dibenz(ox)azepines <i>via</i> Rh(III)-catalyzed cascade regioselective C-H activation/annulation.
Chemical communications (Cambridge, England), 2023, 59, 7751-7754
7131572 CIFC34 H22 Br N O2P 1 21/c 111.7008; 13.1668; 17.7959
90; 106.25; 90
2632.14Naskar, Koushik; Karmakar, Sudip; Mondal, Imtiaj; Sarkar, Writhabrata; Roy, Shantonu; Roy, Anupam; Deb, Indubhusan
Synthesis of indene-fused spiro-dibenz(ox)azepines <i>via</i> Rh(III)-catalyzed cascade regioselective C-H activation/annulation.
Chemical communications (Cambridge, England), 2023, 59, 7751-7754
7131573 CIFC34 H23 N O2P -18.8451; 11.9809; 13.3608
65.259; 74.789; 73.152
1214.4Naskar, Koushik; Karmakar, Sudip; Mondal, Imtiaj; Sarkar, Writhabrata; Roy, Shantonu; Roy, Anupam; Deb, Indubhusan
Synthesis of indene-fused spiro-dibenz(ox)azepines <i>via</i> Rh(III)-catalyzed cascade regioselective C-H activation/annulation.
Chemical communications (Cambridge, England), 2023, 59, 7751-7754
7131574 CIFC30 H29 Cl N O RhP b c a15.3583; 13.3106; 23.5375
90; 90; 90
4811.7Naskar, Koushik; Karmakar, Sudip; Mondal, Imtiaj; Sarkar, Writhabrata; Roy, Shantonu; Roy, Anupam; Deb, Indubhusan
Synthesis of indene-fused spiro-dibenz(ox)azepines <i>via</i> Rh(III)-catalyzed cascade regioselective C-H activation/annulation.
Chemical communications (Cambridge, England), 2023, 59, 7751-7754
7131575 CIFC20 H23 N3 O8C 1 2 121.0745; 12.0391; 9.3014
90; 107.027; 90
2256.49Mo, Nan-Nan; Miao, Yu-Hang; Xiao, Xiao; Hua, Yuan-Zhao; Wang, Min-Can; Huang, Lihua; Mei, Guang-Jian
Catalytic asymmetric <i>de novo</i> construction of 4-pyrrolin-2-ones <i>via</i> intermolecular formal [3+2] cycloaddition of azoalkenes with azlactones.
Chemical communications (Cambridge, England), 2023, 59, 5902-5905
7131576 CIFC24 H33 N O8 S SiP -18.3042; 11.0182; 14.6172
105.403; 96.905; 95.29
1269.23Schifferer, Lukas; Hoppmann, Leon; Groeters, Robin; Mück-Lichtenfeld, Christian; Daniliuc, Constantin G.; García Mancheño, Olga
Divergent access to fused <i>N</i>-heterocycle-thiazolines by solvent-dependent reaction of isoquinolinium thiolates with silylketene acetals.
Chemical communications (Cambridge, England), 2023, 59, 6032-6035
7131577 CIFC30 H28 N2 O2P 1 21/c 113.824; 19.701; 9.478
90; 101.577; 90
2528.8Rao, Qian; Zhang, Yin; Liu, Yin-Ping; Jiang, Bo; Wang, Xiang; Tu, Shu-Jiang; Hao, Wen-Juan
Azofuran activation for annulative rearrangement enabled by gold(I)/Brønsted acid relay catalysis.
Chemical communications (Cambridge, England), 2023, 59, 5725-5728
7131578 CIFC40 H25 B Cl2 F15 N2 PP 1 21/c 111.195; 18.3322; 19.4142
90; 105.076; 90
3847.22Hussain, Zahid; Luo, Yong-An; Wu, Yile; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactivity of frustrated Lewis pairs with BOC protected diazocarboxylates: FLP capture of diazene.
Chemical communications (Cambridge, England), 2023, 59, 6191-6194
7131579 CIFC93 H57 B2 F30 N4 O4P -112.0364; 12.5026; 15.3806
77.149; 78.57; 72.546
2131.08Hussain, Zahid; Luo, Yong-An; Wu, Yile; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactivity of frustrated Lewis pairs with BOC protected diazocarboxylates: FLP capture of diazene.
Chemical communications (Cambridge, England), 2023, 59, 6191-6194
7131580 CIFC31.5 H29 B Cl F15 N O2 PP 21 21 218.0505; 21.0295; 9.8168
90; 90; 90
3726.39Hussain, Zahid; Luo, Yong-An; Wu, Yile; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactivity of frustrated Lewis pairs with BOC protected diazocarboxylates: FLP capture of diazene.
Chemical communications (Cambridge, England), 2023, 59, 6191-6194
7131581 CIFC44.5 H31.75 B F15 N2.25 O2 PP -113.2472; 18.1497; 18.8421
99.604; 106.074; 93.126
4267.8Hussain, Zahid; Luo, Yong-An; Wu, Yile; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactivity of frustrated Lewis pairs with BOC protected diazocarboxylates: FLP capture of diazene.
Chemical communications (Cambridge, England), 2023, 59, 6191-6194
7131582 CIFC16 H20 F3 N3 O4C 1 2 116.38; 6.0768; 18.447
90; 93.389; 90
1833Deka, Jugal Kishore Rai; Borah, Debashree; Das, Paramesh; Sahariah, Biswajit; Vishnoi, Pratap; Sarma, Bani Kanta
Synergistic n → π* and n<sub>N</sub> → π*<sub>Ar</sub> interactions in C-terminal modified prolines: effect on Xaa-Pro <i>cis</i>/<i>trans</i> equilibrium.
Chemical communications (Cambridge, England), 2023, 59, 6080-6083
7131583 CIFC16 H25 N3 O6P 1 21 19.5736; 8.788; 11.6294
90; 106.122; 90
939.94Deka, Jugal Kishore Rai; Borah, Debashree; Das, Paramesh; Sahariah, Biswajit; Vishnoi, Pratap; Sarma, Bani Kanta
Synergistic n → π* and n<sub>N</sub> → π*<sub>Ar</sub> interactions in C-terminal modified prolines: effect on Xaa-Pro <i>cis</i>/<i>trans</i> equilibrium.
Chemical communications (Cambridge, England), 2023, 59, 6080-6083
7131584 CIFC15 H19 N3 O3P 21 21 218.364; 10.6149; 17.5618
90; 90; 90
1559.19Deka, Jugal Kishore Rai; Borah, Debashree; Das, Paramesh; Sahariah, Biswajit; Vishnoi, Pratap; Sarma, Bani Kanta
Synergistic n → π* and n<sub>N</sub> → π*<sub>Ar</sub> interactions in C-terminal modified prolines: effect on Xaa-Pro <i>cis</i>/<i>trans</i> equilibrium.
Chemical communications (Cambridge, England), 2023, 59, 6080-6083
7131585 CIFC16 H18 N4 O3P 21 21 216.8839; 14.6506; 16.5975
90; 90; 90
1673.9Deka, Jugal Kishore Rai; Borah, Debashree; Das, Paramesh; Sahariah, Biswajit; Vishnoi, Pratap; Sarma, Bani Kanta
Synergistic n → π* and n<sub>N</sub> → π*<sub>Ar</sub> interactions in C-terminal modified prolines: effect on Xaa-Pro <i>cis</i>/<i>trans</i> equilibrium.
Chemical communications (Cambridge, England), 2023, 59, 6080-6083
7131586 CIFC20 H34 Cu2 N2 O10P -18.0233; 8.8028; 9.6509
71.076; 86.281; 77.279
628.935Adiyeri Saseendran, Devi Prasad; Fischer, Jörg W A; Müller, Lea; Abbott, Daniel F.; Mougel, Victor; Jeschke, Gunnar; Triana, Carlos A.; Patzke, Greta R.
Copper(II) defect-cubane water oxidation electrocatalysts: from molecular tetramers to oxidic nanostructures.
Chemical communications (Cambridge, England), 2023, 59, 5866-5869
7131587 CIFC104 H180 Cl4 Cu8 N12 O45P 1 21/n 19.1569; 31.5203; 11.7807
90; 97.859; 90
3368.31Adiyeri Saseendran, Devi Prasad; Fischer, Jörg W A; Müller, Lea; Abbott, Daniel F.; Mougel, Victor; Jeschke, Gunnar; Triana, Carlos A.; Patzke, Greta R.
Copper(II) defect-cubane water oxidation electrocatalysts: from molecular tetramers to oxidic nanostructures.
Chemical communications (Cambridge, England), 2023, 59, 5866-5869
7131588 CIFC25 H24 N2 O4P -18.8175; 10.9007; 11.0914
91.044; 101.16; 98.536
1033.11Khot, Nandkishor Prakash; Nagtilak, Prajyot Jayadev; Deo, Nitish Kumar; Kapur, Manmohan
A three component 1,3-difunctionalization of vinyl diazo esters enabled by a cobalt catalyzed C-H activation/carbene migratory insertion.
Chemical communications (Cambridge, England), 2023, 59, 6076-6079
7131589 CIFC23 H34 O4P 1 21/n 19.1816; 23.6417; 10.0047
90; 102.444; 90
2120.69Luo, Yang; Grossman, Robert B.; Nie, Xiao-Bin; Yang, Xing-Wei
Total synthesis and structural reassignment of garcinielliptone FC, a polycyclic polyprenylated acylphloroglucinol with diverse bioactivity.
Chemical communications (Cambridge, England), 2023, 59, 6215-6218
7131590 CIFC48 H32 Cl2 N2 O2P 1 21/c 18.2282; 14.8841; 14.9762
90; 101.424; 90
1797.79Gore, Babasaheb Sopan; Wang, Jeh-Jeng
Visible-light-induced oxidant/additive-free atom-economic synthesis of multifunctionalized cyclopropanes <i>via</i> energy transfer.
Chemical communications (Cambridge, England), 2023, 59, 5878-5881
7131591 CIFC32 H30 O4C 1 2/c 116.1917; 13.3905; 24.2721
90; 105.782; 90
5064.17Gore, Babasaheb Sopan; Wang, Jeh-Jeng
Visible-light-induced oxidant/additive-free atom-economic synthesis of multifunctionalized cyclopropanes <i>via</i> energy transfer.
Chemical communications (Cambridge, England), 2023, 59, 5878-5881
7131592 CIFC24 H21 N OP 1 21/c 17.5385; 12.8334; 18.9919
90; 98.438; 90
1817.47Gore, Babasaheb Sopan; Wang, Jeh-Jeng
Visible-light-induced oxidant/additive-free atom-economic synthesis of multifunctionalized cyclopropanes <i>via</i> energy transfer.
Chemical communications (Cambridge, England), 2023, 59, 5878-5881
7131593 CIFC23 H18 OP 1 21/c 116.1546; 5.9286; 16.4487
90; 94.338; 90
1570.85Gore, Babasaheb Sopan; Wang, Jeh-Jeng
Visible-light-induced oxidant/additive-free atom-economic synthesis of multifunctionalized cyclopropanes <i>via</i> energy transfer.
Chemical communications (Cambridge, England), 2023, 59, 5878-5881
7131594 CIFC18 H13 O PP 1 21/c 110.025; 9.5951; 14.1127
90; 93.226; 90
1355.4Koellner, Connor A.; Reid, Amelia G.; Machan, Charles W.
Co-electrocatalytic CO<sub>2</sub> reduction mediated by a dibenzophosphole oxide and a chromium complex.
Chemical communications (Cambridge, England), 2023, 59, 6359-6362
7131595 CIFC24 H48 N2C 1 2/c 118.4911; 8.063; 15.8001
90; 96.727; 90
2339.5Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mandal, Debdeep; Das, Ayan; Ramakrishnan, Raghunathan; Mote, Kaustubh R.; Schulzke, Carola; Yildiz, Cem Burak; Jana, Anukul
Reduction of 2-<i>H</i>-substituted pyrrolinium cations: the carbon-carbon single bond in air stable 2,2'-bipyrrolidines as a two-electron-source.
Chemical communications (Cambridge, England), 2023, 59, 6698-6701
7131596 CIFC40 H64 N2C 1 2/c 119.98; 9.5392; 20.618
90; 115.474; 90
3547.6Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mandal, Debdeep; Das, Ayan; Ramakrishnan, Raghunathan; Mote, Kaustubh R.; Schulzke, Carola; Yildiz, Cem Burak; Jana, Anukul
Reduction of 2-<i>H</i>-substituted pyrrolinium cations: the carbon-carbon single bond in air stable 2,2'-bipyrrolidines as a two-electron-source.
Chemical communications (Cambridge, England), 2023, 59, 6698-6701
7131597 CIFC56 H48 I2 N2 O8 S4P -19.2544; 9.7531; 30.479
89.135; 88.15; 74.562
2650.31Mutra, Mohana Reddy; Li, Jing; Wang, Jeh-Jeng
Light-mediated sulfonyl-iodination of ynamides and internal alkynes.
Chemical communications (Cambridge, England), 2023, 59, 6584-6587
7131598 CIFC22 H17 I O4 SP -17.9819; 9.8435; 13.6204
82.881; 74.573; 74.145
990.83Mutra, Mohana Reddy; Li, Jing; Wang, Jeh-Jeng
Light-mediated sulfonyl-iodination of ynamides and internal alkynes.
Chemical communications (Cambridge, England), 2023, 59, 6584-6587
7131599 CIFC22 H19 I O4 S2P -16.788; 12.1573; 13.6372
96.973; 96.425; 102.531
1079.3Mutra, Mohana Reddy; Li, Jing; Wang, Jeh-Jeng
Light-mediated sulfonyl-iodination of ynamides and internal alkynes.
Chemical communications (Cambridge, England), 2023, 59, 6584-6587
7131600 CIFC50 H52 I2 N2 O8 S4P -18.5557; 10.3154; 29.9202
93.058; 96.826; 104.064
2534Mutra, Mohana Reddy; Li, Jing; Wang, Jeh-Jeng
Light-mediated sulfonyl-iodination of ynamides and internal alkynes.
Chemical communications (Cambridge, England), 2023, 59, 6584-6587
7131601 CIFC20 H24 O SP 1 21/c 120.6821; 14.2922; 5.8697
90; 92.44; 90
1733.5Cui, Wenwen; Guo, Guoju; Wang, Yifei; Song, Xiuyan; Lv, Jian; Yang, Daoshan
Visible light/copper catalysis enabled alkylation of silyl enol ethers with arylsulfonium salts.
Chemical communications (Cambridge, England), 2023, 59, 6367-6370
7131602 CIFC26 H30 N4 OP 1 21/c 110.5205; 21.234; 10.031
90; 90.914; 90
2240.6Kong, Lingheng; Han, Xi; Hu, Panjie; Wang, Fen; Li, Xingwei
Three-component regioselective carboamidation of 1,3-enynes <i>via</i> rhodium(III)-catalyzed C-H activation.
Chemical communications (Cambridge, England), 2023, 59, 6690-6693
7131603 CIFC28 H28 N4 OP 1 21 19.9949; 8.8643; 14.6922
90; 107.946; 90
1238.4Kong, Lingheng; Han, Xi; Hu, Panjie; Wang, Fen; Li, Xingwei
Three-component regioselective carboamidation of 1,3-enynes <i>via</i> rhodium(III)-catalyzed C-H activation.
Chemical communications (Cambridge, England), 2023, 59, 6690-6693
7131604 CIFC42 H114 Si12 Sn6P -113.2745; 13.7262; 22.639
86.4949; 76.8746; 72.0005
3820.46Mears, Kristian L.; Ruiz, Bronson; Nguyen, Gia-Ann; Zou, Wenxing; Fettinger, James C.; Power, Philip P.
Disproportionation of Sn(II){CH(SiMe<sub>3</sub>)<sub>2</sub>}<sub>2</sub> to ˙Sn(III){CH(SiMe<sub>3</sub>)<sub>2</sub>}<sub>3</sub> and ˙Sn(I){CH(SiMe<sub>3</sub>)<sub>2</sub>}: characterization of the Sn(I) product.
Chemical communications (Cambridge, England), 2023, 59, 6399-6402
7131605 CIFC27 H54 Cu4 I6 O13 Rb2P n m a30.888; 15.243; 10.929
90; 90; 90
5146Almushaikeh, Alaa M.; Wang, Hong; Gutiérrez-Arzaluz, Luis; Yin, Jun; Huang, Ren-Wu; Bakr, Osman M.; Mohammed, Omar F.
Zero-dimensional Cu(I)-based organometallic halide with green cluster-centred emission for high resolution X-ray imaging screens.
Chemical communications (Cambridge, England), 2023, 59, 4447-4450
7131606 CIFC88 H86 Cl3 N9 O18 Zn2P 111.0621; 13.6834; 15.7489
77.7324; 71.3068; 68.6923
2091.27Penasa, Roberto; Begato, Federico; Licini, Giulia; Wurst, Klaus; Abbate, Sergio; Longhi, Giovanna; Zonta, Cristiano
Fluorescence detected circular dichroism (FDCD) of a stereodynamic probe.
Chemical communications (Cambridge, England), 2023, 59, 6714-6717
7131607 CIFC16 H14 Br2 F6 N2 O3P 1 n 18.5935; 10.4364; 10.8779
90; 94.61; 90
972.43Luo, Xian; Xu, Meng-Meng; Xu, Xiao-Ping; Ji, Shun-Jun
NBS-induced intramolecular annulation reactions for the divergent synthesis of fused- and spirocyclic indolines.
Chemical communications (Cambridge, England), 2023, 59, 6576-6579
7131608 CIFC18 H15 F N2 O2P 1 21/c 111.1831; 11.7646; 12.1011
90; 103.533; 90
1547.9Luo, Xian; Xu, Meng-Meng; Xu, Xiao-Ping; Ji, Shun-Jun
NBS-induced intramolecular annulation reactions for the divergent synthesis of fused- and spirocyclic indolines.
Chemical communications (Cambridge, England), 2023, 59, 6576-6579
7131609 CIFC28 H0.5 N6 O12 Zn2.5P -113.316; 13.775; 14.849
107.422; 101.816; 95.038
2511.1Yang, Fan; Xue, Juan-Juan; Lei, Guang-Ping; Zhang, Wen-Yan; Yang, Guo-Ping; Wang, Yao-Yu
Efficient C<sub>2</sub>H<sub>2</sub>-selective separation in a microporous Zn(II)-based metal-organic framework <i>via</i> the dual-ligand strategy.
Chemical communications (Cambridge, England), 2023, 59, 6403-6406
7131610 CIFC36 H24 N2 O2P 1 21/c 110.7134; 12.6341; 10.023
90; 107.382; 90
1294.7Berthe, Mathilde; Kagawa, Yoshiyuki; Riquet, Axel; Hayashi, Takashi; Weiss, Jean; Wytko, Jennifer A.
Remote template effect in the synthesis of bipyridine-strapped porphyrins.
Chemical communications (Cambridge, England), 2023, 59, 6718-6721
7131611 CIFC60 H46 N6P 1 21/c 112.0156; 15.3535; 24.3972
90; 93.173; 90
4493.9Berthe, Mathilde; Kagawa, Yoshiyuki; Riquet, Axel; Hayashi, Takashi; Weiss, Jean; Wytko, Jennifer A.
Remote template effect in the synthesis of bipyridine-strapped porphyrins.
Chemical communications (Cambridge, England), 2023, 59, 6718-6721
7131612 CIFC58 H40 Cl2 N6 O ZnP 1 21/n 112.0783; 13.7262; 27.7976
90; 102.461; 90
4500Berthe, Mathilde; Kagawa, Yoshiyuki; Riquet, Axel; Hayashi, Takashi; Weiss, Jean; Wytko, Jennifer A.
Remote template effect in the synthesis of bipyridine-strapped porphyrins.
Chemical communications (Cambridge, England), 2023, 59, 6718-6721
7131613 CIFC91 H64 Cl2 N8 O2P -113.281; 13.2984; 20.8307
80.431; 89.27; 79.49
3566.4Berthe, Mathilde; Kagawa, Yoshiyuki; Riquet, Axel; Hayashi, Takashi; Weiss, Jean; Wytko, Jennifer A.
Remote template effect in the synthesis of bipyridine-strapped porphyrins.
Chemical communications (Cambridge, England), 2023, 59, 6718-6721
7131614 CIFC104.85 H58.16 N6.68 O4.66 S0.44P 1 21/n 115.004; 17.383; 28.473
90; 91.101; 90
7425Hashikawa, Yoshifumi; Sadai, Shumpei; Murata, Yasujiro
Bilateral π-extension of an open-[60]fullerene in a helical manner.
Chemical communications (Cambridge, England), 2023, 59, 6560-6563
7131615 CIFC94.5 H28 N2 O5 S5P -113.25; 13.47; 17.15
82.98; 80.57; 80.95
2967Hashikawa, Yoshifumi; Sadai, Shumpei; Murata, Yasujiro
Synthesis of open-[70]fullerenes bearing huge orifices.
Chemical communications (Cambridge, England), 2023, 59, 7387-7390
7131616 CIFC24 H21 N3 O6 SP 1 21/n 110.8433; 8.3762; 25.2432
90; 100.313; 90
2255.7Zhong, Zukang; Liao, Lihua; Liu, Yunyun; Zhang, Ming; Wan, Jie-Ping
Annulation of enaminones with quinonediimides/quinoneimides for selective synthesis of indoles and 2-aminobenzofurans.
Chemical communications (Cambridge, England), 2023, 59, 6885-6888
7131617 CIFC28 H22 Cl NP 1 21/c 19.2102; 20.916; 11.778
90; 102.6; 90
2214.3Ghasemi, Mehran; Rahimi, Banafshe; Dehghan, Maryam; Bernoosha, Mohammad Hossein; Jafarpour, Farnaz
<i>Syn</i>- <i>versus anti</i>-carbopalladation of alkynes with organoborons: access to indoles symmetrically and unsymmetrically substituted on their 2,3-positions.
Chemical communications (Cambridge, England), 2023, 59, 6873-6876
7131618 CIFC28 H23 N OP 1 21/c 110.887; 9.942; 19.661
90; 92.94; 90
2125.3Ghasemi, Mehran; Rahimi, Banafshe; Dehghan, Maryam; Bernoosha, Mohammad Hossein; Jafarpour, Farnaz
<i>Syn</i>- <i>versus anti</i>-carbopalladation of alkynes with organoborons: access to indoles symmetrically and unsymmetrically substituted on their 2,3-positions.
Chemical communications (Cambridge, England), 2023, 59, 6873-6876
7131619 CIFC28 H23 N O2P -18.0268; 11.315; 12.532
73.63; 86.31; 86.29
1088.5Ghasemi, Mehran; Rahimi, Banafshe; Dehghan, Maryam; Bernoosha, Mohammad Hossein; Jafarpour, Farnaz
<i>Syn</i>- <i>versus anti</i>-carbopalladation of alkynes with organoborons: access to indoles symmetrically and unsymmetrically substituted on their 2,3-positions.
Chemical communications (Cambridge, England), 2023, 59, 6873-6876
7131620 CIFC13 H15 N5 O PtP b c m11.4912; 18.9552; 6.5717
90; 90; 90
1431.43Sasaki, Kono; Saito, Daisuke; Yoshida, Masaki; Tanaka, Fuka; Kobayashi, Atsushi; Sada, Kazuki; Kato, Masako
Chromic triboluminescence of self-assembled platinum(II) complexes.
Chemical communications (Cambridge, England), 2023, 59, 6745-6748
7131621 CIFC15 H17 N5 PtP -16.9511; 9.3228; 11.6052
88.898; 84.088; 87.195
747.09Sasaki, Kono; Saito, Daisuke; Yoshida, Masaki; Tanaka, Fuka; Kobayashi, Atsushi; Sada, Kazuki; Kato, Masako
Chromic triboluminescence of self-assembled platinum(II) complexes.
Chemical communications (Cambridge, England), 2023, 59, 6745-6748
7131622 CIFC14 H15 N5 PtP -17.0539; 9.1957; 11.0803
89.036; 86.526; 89.72
717.3Sasaki, Kono; Saito, Daisuke; Yoshida, Masaki; Tanaka, Fuka; Kobayashi, Atsushi; Sada, Kazuki; Kato, Masako
Chromic triboluminescence of self-assembled platinum(II) complexes.
Chemical communications (Cambridge, England), 2023, 59, 6745-6748
7131623 CIFC13 H13 N5 PtP 21 21 2113.7509; 17.8898; 21.4801
90; 90; 90
5284.12Sasaki, Kono; Saito, Daisuke; Yoshida, Masaki; Tanaka, Fuka; Kobayashi, Atsushi; Sada, Kazuki; Kato, Masako
Chromic triboluminescence of self-assembled platinum(II) complexes.
Chemical communications (Cambridge, England), 2023, 59, 6745-6748
7131624 CIFC35 H51 F6 N2 Nd O6P -19.5877; 10.4329; 21.9228
83.768; 77.981; 65.249
1947.22Hu, Guojun; Wang, Yanwei; Wang, Yaorong; Zhu, Xuehua; Yuan, Dan; Yao, Yingming
Random copolymerization of trimethylene carbonate with L-lactide initiated by amine-bridged bis(phenolate) neodymium alkoxides.
Chemical communications (Cambridge, England), 2023, 59, 6921-6924
7131625 CIFC42 H68 F3 N2 Nd O8P -111.4516; 17.9776; 21.6593
99.326; 92.638; 90.353
4395Hu, Guojun; Wang, Yanwei; Wang, Yaorong; Zhu, Xuehua; Yuan, Dan; Yao, Yingming
Random copolymerization of trimethylene carbonate with L-lactide initiated by amine-bridged bis(phenolate) neodymium alkoxides.
Chemical communications (Cambridge, England), 2023, 59, 6921-6924
7131626 CIFC25 H18 N2 O SP b c a8.3336; 18.5187; 26.3322
90; 90; 90
4063.8Dhara, Hirendra Nath; Rakshit, Amitava; Barik, Dinabandhu; Ghosh, Koustuv; Patel, Bhisma K.
Visible-light driven electron-donor-acceptor (EDA) complex-initiated synthesis of thio-functionalized pyridines.
Chemical communications (Cambridge, England), 2023, 59, 7990-7993
7131627 CIFC18 H18 O5P b c a8.8205; 18.733; 19.9045
90; 90; 90
3288.9Srinivas, Dasari; Mounika, Kurella; Satyanarayana, Gedu
Functionalization of arylacetic acids <i>via</i> directing-group-assisted remote <i>meta</i>-C-H activation.
Chemical communications (Cambridge, England), 2023, 59, 7084-7087
7131628 CIFC32 H27 N O4 S2P 1 21/n 115.0121; 13.2954; 15.133
90; 113.157; 90
2777.1Meena, Shivam A.; Sharma, Poonam; Verma, Akhilesh K.
Stereoselective synthesis of difunctionalized succinimides from aza-1,6-enynes by radical cascade reaction.
Chemical communications (Cambridge, England), 2023, 59, 7271-7274
7131629 CIFC32 H26 Cl N O4 S SeP 1 21/n 17.8375; 15.8427; 22.6838
90; 99.443; 90
2778.4Meena, Shivam A.; Sharma, Poonam; Verma, Akhilesh K.
Stereoselective synthesis of difunctionalized succinimides from aza-1,6-enynes by radical cascade reaction.
Chemical communications (Cambridge, England), 2023, 59, 7271-7274
7131630 CIFC24 H19 Cl N2 OP 1 21/c 111.2188; 20.7777; 8.83
90; 109.93; 90
1935.01Li, Cheng; Zhao, Bin; Mao, Guojiang; Deng, Guo-Jun
Rhodium(III)-catalyzed mild and regioselective dearomative spirocyclization of 2-aryl-3-nitrosoindoles with alkynes.
Chemical communications (Cambridge, England), 2023, 59, 7044-7047
7131631 CIFC31 H22 N2 OP -110.2696; 10.3708; 12.6585
90.132; 110.122; 104.018
1222.8Li, Cheng; Zhao, Bin; Mao, Guojiang; Deng, Guo-Jun
Rhodium(III)-catalyzed mild and regioselective dearomative spirocyclization of 2-aryl-3-nitrosoindoles with alkynes.
Chemical communications (Cambridge, England), 2023, 59, 7044-7047
7131632 CIFC20 H25 Cl N O3 PP -18.6173; 9.9762; 13.012
75.004; 89.623; 65.828
979.49Kaboudin, Babak; Ghashghaee, Mojtaba; Fukaya, Haruhiko; Yanai, Hikaru
Stereoselective synthesis of vinylphosphonates through aromatic aza-Claisen rearrangement of α-aminophosphonates.
Chemical communications (Cambridge, England), 2023, 59, 7076-7079
7131633 CIFC21 H28 N O4 PP 1 21 19.8383; 9.6582; 10.9876
90; 102.287; 90
1020.13Kaboudin, Babak; Ghashghaee, Mojtaba; Fukaya, Haruhiko; Yanai, Hikaru
Stereoselective synthesis of vinylphosphonates through aromatic aza-Claisen rearrangement of α-aminophosphonates.
Chemical communications (Cambridge, England), 2023, 59, 7076-7079
7131634 CIFC104 H92 N4 O8 S4 Zn4P -113.5602; 13.8377; 14.8499
70.109; 81.732; 72.621
2497.85Borys, Andryj M.; Kunzmann, Tim; Gil-Negrete, Jose M; Hevia, Eva
Atom-efficient arylation of <i>N</i>-tosylimines mediated by cooperative ZnAr<sub>2</sub>/Zn(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> combinations.
Chemical communications (Cambridge, England), 2023, 59, 7583-7586
7131635 CIFC32 H39 N3 O2 S ZnC 1 2/c 128.6033; 9.8468; 23.6134
90; 94.965; 90
6625.8Borys, Andryj M.; Kunzmann, Tim; Gil-Negrete, Jose M; Hevia, Eva
Atom-efficient arylation of <i>N</i>-tosylimines mediated by cooperative ZnAr<sub>2</sub>/Zn(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> combinations.
Chemical communications (Cambridge, England), 2023, 59, 7583-7586
7131636 CIFC26 H13 F10 N O2 S ZnP 1 21/n 111.6712; 16.9909; 12.479
90; 92.27; 90
2472.7Borys, Andryj M.; Kunzmann, Tim; Gil-Negrete, Jose M; Hevia, Eva
Atom-efficient arylation of <i>N</i>-tosylimines mediated by cooperative ZnAr<sub>2</sub>/Zn(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> combinations.
Chemical communications (Cambridge, England), 2023, 59, 7583-7586
7131637 CIFC76 H46 F20 N2 O4 S2 Zn4P 1 21/n 112.61445; 17.36835; 15.87255
90; 93.2751; 90
3471.87Borys, Andryj M.; Kunzmann, Tim; Gil-Negrete, Jose M; Hevia, Eva
Atom-efficient arylation of <i>N</i>-tosylimines mediated by cooperative ZnAr<sub>2</sub>/Zn(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub> combinations.
Chemical communications (Cambridge, England), 2023, 59, 7583-7586
7131638 CIFC25 H21 Cl N2 O3 SP -110.012; 10.023; 11.978
94.38; 109.83; 93.94
1121.7Baidya, Ramlal; Das, Prasenjit; Pratihar, Pintu; Maiti, Dilip K.
Ring expansion and fused cyclization catalysis to construct indoloquinazolinones with functionalization.
Chemical communications (Cambridge, England), 2023, 59, 7978-7981
7131639 CIFC23 H19 N O3P -17.9054; 13.1683; 19.1538
90.215; 96.665; 106.787
1894.59Sun, Weiqiang; Cui, Xueli; Qu, Jing; Cai, Xiaojia; Hu, Jinhui; Xiong, Zhuang; Guo, Suqin; Xu, Jun; Chen, Wen-Hua; Wu, Jia-Qiang
Facile access to 2-hydroxy-2-substituted indole-3-ones <i>via</i> a copper-catalyzed oxidative cyclization of 2-arylethynylanilines.
Chemical communications (Cambridge, England), 2023, 59, 7228-7231
7131640 CIFC17 H14 Br N O4C 1 2/c 124.4178; 5.7091; 26.1253
90; 112.314; 90
3369.24Sun, Weiqiang; Cui, Xueli; Qu, Jing; Cai, Xiaojia; Hu, Jinhui; Xiong, Zhuang; Guo, Suqin; Xu, Jun; Chen, Wen-Hua; Wu, Jia-Qiang
Facile access to 2-hydroxy-2-substituted indole-3-ones <i>via</i> a copper-catalyzed oxidative cyclization of 2-arylethynylanilines.
Chemical communications (Cambridge, England), 2023, 59, 7228-7231
7131641 CIFC21 H26 N2 O2 SP 1 21/c 18.684; 16.4916; 13.6197
90; 92.3; 90
1948.95Yadav, Suman; Kant, Ruchir; Kuram, Malleswara Rao
Metal-free transfer hydrogenation/cycloaddition cascade of activated quinolines and isoquinolines with tosyl azides.
Chemical communications (Cambridge, England), 2023, 59, 7088-7091
7131642 CIFC23 H22 N2 O2 SP b c a15.7372; 13.4885; 18.8423
90; 90; 90
3999.68Yadav, Suman; Kant, Ruchir; Kuram, Malleswara Rao
Metal-free transfer hydrogenation/cycloaddition cascade of activated quinolines and isoquinolines with tosyl azides.
Chemical communications (Cambridge, England), 2023, 59, 7088-7091
7131643 CIFC33 H28 F N O3P 1 21 19.5394; 11.1681; 12.3498
90; 101.756; 90
1288.1Miao, Yu-Hang; Hua, Yuan-Zhao; Jia, Shi-Kun; Xiao, Xiao; Wang, Min-Can; Mei, Guang-Jian
Zn-ProPhenol catalyzed asymmetric inverse-electron-demand Diels-Alder reaction.
Chemical communications (Cambridge, England), 2023, 59, 6929-6932
7131644 CIFC41 H36 Cl2 O4I 1 2/a 18.0242; 30.1775; 13.9999
90; 105.072; 90
3273.46Čavlović, Daniel; Blacque, Olivier; Krummenacher, Ivo; Braunschweig, Holger; Ravat, Prince; Juríček, Michal
Dimethylnonacethrene - <i>en route</i> to a magnetic switch.
Chemical communications (Cambridge, England), 2023, 59, 7743-7746
7131645 CIFC38 H26 O2P -18.1425; 12.3731; 13.4276
71.82; 73.113; 74.791
1207.72Čavlović, Daniel; Blacque, Olivier; Krummenacher, Ivo; Braunschweig, Holger; Ravat, Prince; Juríček, Michal
Dimethylnonacethrene - <i>en route</i> to a magnetic switch.
Chemical communications (Cambridge, England), 2023, 59, 7743-7746
7131646 CIFC78 H78P 1 c 118.35075; 9.98785; 16.08593
90; 91.0918; 90
2947.77Čavlović, Daniel; Blacque, Olivier; Krummenacher, Ivo; Braunschweig, Holger; Ravat, Prince; Juríček, Michal
Dimethylnonacethrene - <i>en route</i> to a magnetic switch.
Chemical communications (Cambridge, England), 2023, 59, 7743-7746
7131647 CIFC42 H50 Co N4 S6P 1 21/n 116.9834; 16.3415; 17.0437
90; 116.574; 90
4230.5Hou, Qin; Chen, Li-Jun; He, Jing; Chen, Er-Xia; Wang, Bo; Zhou, Xuechou; Dai, Yumei; He, Liang; Lin, Qipu
Thiophenol-spaced 2D coordination polymers with extraordinary alkali resistance and efficient photothermal conversion.
Chemical communications (Cambridge, England), 2023, 59, 7072-7075
7131648 CIFC84 H108 N8 S12 Zn2I 41/a :211.35023; 11.35023; 34.2177
90; 90; 90
4408.19Hou, Qin; Chen, Li-Jun; He, Jing; Chen, Er-Xia; Wang, Bo; Zhou, Xuechou; Dai, Yumei; He, Liang; Lin, Qipu
Thiophenol-spaced 2D coordination polymers with extraordinary alkali resistance and efficient photothermal conversion.
Chemical communications (Cambridge, England), 2023, 59, 7072-7075
7131649 CIFC42 H50 Fe N4 S6P 1 21/n 116.9805; 16.3895; 17.0828
90; 116.751; 90
4245.3Hou, Qin; Chen, Li-Jun; He, Jing; Chen, Er-Xia; Wang, Bo; Zhou, Xuechou; Dai, Yumei; He, Liang; Lin, Qipu
Thiophenol-spaced 2D coordination polymers with extraordinary alkali resistance and efficient photothermal conversion.
Chemical communications (Cambridge, England), 2023, 59, 7072-7075
7131650 CIFC24 H19 Cl N2P 1 21/c 18.90415; 28.9401; 7.98398
90; 111.116; 90
1919.23Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
The emission efficiency of cationic solid state luminophores is directly proportional to the intermolecular charge transfer intensity.
Chemical communications (Cambridge, England), 2023, 59, 6905-6908
7131651 CIFC64 H70 Cl2 N4P 1 21/n 110.2702; 12.6758; 41.47
90; 90.17; 90
5398.7Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
The emission efficiency of cationic solid state luminophores is directly proportional to the intermolecular charge transfer intensity.
Chemical communications (Cambridge, England), 2023, 59, 6905-6908
7131652 CIFC54 H52 N4 O6 S2P -113.3101; 13.4723; 13.9252
101.733; 102.111; 100.527
2323.26Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
The emission efficiency of cationic solid state luminophores is directly proportional to the intermolecular charge transfer intensity.
Chemical communications (Cambridge, England), 2023, 59, 6905-6908
7131653 CIFC32 H35 Cl N2 O4P b c a12.143; 11.0905; 42.6477
90; 90; 90
5743.4Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
The emission efficiency of cationic solid state luminophores is directly proportional to the intermolecular charge transfer intensity.
Chemical communications (Cambridge, England), 2023, 59, 6905-6908
7131654 CIFC25 H22 N2 O3 SP 1 21/c 114.975; 19.7881; 14.8102
90; 108.774; 90
4155.16Leduskrasts, Kaspars; Kinens, Artis; Suna, Edgars
The emission efficiency of cationic solid state luminophores is directly proportional to the intermolecular charge transfer intensity.
Chemical communications (Cambridge, England), 2023, 59, 6905-6908
7131655 CIFC60 H108 Ge3 N6P 1 21/n 115.4003; 14.5568; 29.3234
90; 105.105; 90
6346.57Caise, Alexa; Hicks, Jamie; Heilmann, Andreas; Aldridge, Simon
Redox flexibility in a germanium hydride manifold: hydrogen shuttling <i>via</i> oxidative addition and reductive elimination.
Chemical communications (Cambridge, England), 2023, 59, 7251-7254
7131656 CIFC30 H42 Ge N2 OP -18.2011; 10.5814; 16.5784
102.491; 100.285; 93.091
1375.61Caise, Alexa; Hicks, Jamie; Heilmann, Andreas; Aldridge, Simon
Redox flexibility in a germanium hydride manifold: hydrogen shuttling <i>via</i> oxidative addition and reductive elimination.
Chemical communications (Cambridge, England), 2023, 59, 7251-7254
7131657 CIFC21 H36 Ge N2 O2P 1 21/n 114.3981; 11.3783; 14.8745
90; 118.729; 90
2136.86Caise, Alexa; Hicks, Jamie; Heilmann, Andreas; Aldridge, Simon
Redox flexibility in a germanium hydride manifold: hydrogen shuttling <i>via</i> oxidative addition and reductive elimination.
Chemical communications (Cambridge, England), 2023, 59, 7251-7254
7131658 CIFC47 H44 B F20 Ge N2P b c a18.1855; 22.2471; 22.8462
90; 90; 90
9243Caise, Alexa; Hicks, Jamie; Heilmann, Andreas; Aldridge, Simon
Redox flexibility in a germanium hydride manifold: hydrogen shuttling <i>via</i> oxidative addition and reductive elimination.
Chemical communications (Cambridge, England), 2023, 59, 7251-7254
7131659 CIFC16 H22 Br4 F2 N2 PbP 21 21 217.8431; 8.7977; 33.4343
90; 90; 90
2307.01Zhao, Xuan-Hui; Li, Na-Na; Peng, Jing; Xu, Jun; Luo, Peng; Dong, Xi-Yan; Hu, Xiaozong
Circularly polarized luminescence enlargement from crystals to oriented films of enantiopure 2D hybrid perovskites.
Chemical communications (Cambridge, England), 2023, 59, 6881-6884
7131660 CIFC16 H22 Br4 F2 N2 PbP 21 21 217.8403; 8.7958; 33.4329
90; 90; 90
2305.59Zhao, Xuan-Hui; Li, Na-Na; Peng, Jing; Xu, Jun; Luo, Peng; Dong, Xi-Yan; Hu, Xiaozong
Circularly polarized luminescence enlargement from crystals to oriented films of enantiopure 2D hybrid perovskites.
Chemical communications (Cambridge, England), 2023, 59, 6881-6884
7131661 CIFC64 H92 Br14 F8 N8 O2 Pb3P -18.1612; 17.5034; 18.6108
115.736; 102.225; 95.098
2290.62Zhao, Xuan-Hui; Li, Na-Na; Peng, Jing; Xu, Jun; Luo, Peng; Dong, Xi-Yan; Hu, Xiaozong
Circularly polarized luminescence enlargement from crystals to oriented films of enantiopure 2D hybrid perovskites.
Chemical communications (Cambridge, England), 2023, 59, 6881-6884
7131662 CIFC50 H64 N4 O14P -19.483; 10.987; 12.79
68.707; 82.307; 73.621
1190.5Li, Shi-Yao; Yao, Huan; Hu, Hao; Chen, Wen-Jie; Yang, Liu-Pan; Wang, Li-Li
Selective adsorption of trace morpholine impurities over <i>N</i>-ethyl morpholine by tetralactam solids.
Chemical communications (Cambridge, England), 2023, 59, 7204-7207
7131663 CIFC64 H84 N8 O12P -111.4061; 11.5234; 13.0536
84.464; 65.455; 74.125
1500.87Li, Shi-Yao; Yao, Huan; Hu, Hao; Chen, Wen-Jie; Yang, Liu-Pan; Wang, Li-Li
Selective adsorption of trace morpholine impurities over <i>N</i>-ethyl morpholine by tetralactam solids.
Chemical communications (Cambridge, England), 2023, 59, 7204-7207
7131664 CIFC23 H27 F2 N O2 S4P -16.0073; 11.365; 18.1482
99.599; 90.858; 94.491
1217.44Wang, Baoxu; Hu, Zijing; Huang, Lu; Ren, Xiaorui; Gao, Qianwen; Wang, Xi
Polysulfide synthesis <i>via</i> visible-light-induced heteroarene-migratory dithiosulfonylation reaction.
Chemical communications (Cambridge, England), 2023, 59, 7247-7250
7131665 CIFC14 N2 SP b c a11.807; 10.063; 21.134
90; 90; 90
2511Wang, Baoxu; Hu, Zijing; Huang, Lu; Ren, Xiaorui; Gao, Qianwen; Wang, Xi
Polysulfide synthesis <i>via</i> visible-light-induced heteroarene-migratory dithiosulfonylation reaction.
Chemical communications (Cambridge, England), 2023, 59, 7247-7250
7131666 CIFC42 H41 SiP -19.5487; 11.5708; 15.9662
70.66; 80.85; 74.74
1600.8Janssen, Marvin; Mebs, Stefan; Beckmann, Jens
Aryldimethylelement cations of the heavier group 14 elements. An essentially three-coordinate plumbylium ion.
Chemical communications (Cambridge, England), 2023, 59, 7267-7270
7131667 CIFC49 H47 Cl SnP -19.415; 13.8081; 15.8413
82.746; 81.826; 70.414
1913.7Janssen, Marvin; Mebs, Stefan; Beckmann, Jens
Aryldimethylelement cations of the heavier group 14 elements. An essentially three-coordinate plumbylium ion.
Chemical communications (Cambridge, England), 2023, 59, 7267-7270
7131668 CIFC66 H39 B F20 SnP -112.6763; 12.9768; 17.9122
86.226; 84.228; 84.387
2912.9Janssen, Marvin; Mebs, Stefan; Beckmann, Jens
Aryldimethylelement cations of the heavier group 14 elements. An essentially three-coordinate plumbylium ion.
Chemical communications (Cambridge, England), 2023, 59, 7267-7270
7131669 CIFC43 H42 PbP -110.137; 12.5545; 15.8115
101.75; 96.006; 109.536
1823.8Janssen, Marvin; Mebs, Stefan; Beckmann, Jens
Aryldimethylelement cations of the heavier group 14 elements. An essentially three-coordinate plumbylium ion.
Chemical communications (Cambridge, England), 2023, 59, 7267-7270
7131670 CIFC66 H39 B F20 SiP 1 21/n 110.5128; 17.7699; 29.707
90; 94.346; 90
5533.6Janssen, Marvin; Mebs, Stefan; Beckmann, Jens
Aryldimethylelement cations of the heavier group 14 elements. An essentially three-coordinate plumbylium ion.
Chemical communications (Cambridge, England), 2023, 59, 7267-7270
7131671 CIFC66 H39 B F20 PbP -110.2803; 14.774; 18.3384
86.552; 78.805; 85.707
2721.6Janssen, Marvin; Mebs, Stefan; Beckmann, Jens
Aryldimethylelement cations of the heavier group 14 elements. An essentially three-coordinate plumbylium ion.
Chemical communications (Cambridge, England), 2023, 59, 7267-7270
7131672 CIFC56 H34 Cl4 O8P 1 21/c 17.5511; 11.4435; 26.3091
90; 92.902; 90
2270.5Hashimoto, Taito; Oketani, Ryusei; Inoue, Asato; Okubo, Kohei; Oka, Kouki; Tohnai, Norimitsu; Kamiya, Kazuhide; Nakanishi, Shuji; Hisaki, Ichiro
Statically and dynamically flexible hydrogen-bonded frameworks based on 4,5,9,10-tetrakis(4-carboxyphenyl)pyrene.
Chemical communications (Cambridge, England), 2023, 59, 7224-7227
7131673 CIFC44 H26 O8P -17.5864; 9.404; 13.016
78.06; 86.453; 67.84
841.3Hashimoto, Taito; Oketani, Ryusei; Inoue, Asato; Okubo, Kohei; Oka, Kouki; Tohnai, Norimitsu; Kamiya, Kazuhide; Nakanishi, Shuji; Hisaki, Ichiro
Statically and dynamically flexible hydrogen-bonded frameworks based on 4,5,9,10-tetrakis(4-carboxyphenyl)pyrene.
Chemical communications (Cambridge, England), 2023, 59, 7224-7227
7131674 CIFC56 H32 Cl6 O8C 1 2/m 127.5399; 11.8206; 7.2355
90; 92.898; 90
2352.4Hashimoto, Taito; Oketani, Ryusei; Inoue, Asato; Okubo, Kohei; Oka, Kouki; Tohnai, Norimitsu; Kamiya, Kazuhide; Nakanishi, Shuji; Hisaki, Ichiro
Statically and dynamically flexible hydrogen-bonded frameworks based on 4,5,9,10-tetrakis(4-carboxyphenyl)pyrene.
Chemical communications (Cambridge, England), 2023, 59, 7224-7227
7131675 CIFC44 H26 O8C 1 2/m 123.482; 17.2143; 7.5294
90; 94.013; 90
3036.1Hashimoto, Taito; Oketani, Ryusei; Inoue, Asato; Okubo, Kohei; Oka, Kouki; Tohnai, Norimitsu; Kamiya, Kazuhide; Nakanishi, Shuji; Hisaki, Ichiro
Statically and dynamically flexible hydrogen-bonded frameworks based on 4,5,9,10-tetrakis(4-carboxyphenyl)pyrene.
Chemical communications (Cambridge, England), 2023, 59, 7224-7227
7131676 CIFC44 H26 O8P 1 21/c 16.7428; 15.8023; 27.6306
90; 93.044; 90
2939.9Hashimoto, Taito; Oketani, Ryusei; Inoue, Asato; Okubo, Kohei; Oka, Kouki; Tohnai, Norimitsu; Kamiya, Kazuhide; Nakanishi, Shuji; Hisaki, Ichiro
Statically and dynamically flexible hydrogen-bonded frameworks based on 4,5,9,10-tetrakis(4-carboxyphenyl)pyrene.
Chemical communications (Cambridge, England), 2023, 59, 7224-7227
7131677 CIFC68 H59 N3 O8P 1 21/c 17.4693; 14.233; 24.172
90; 94.08; 90
2563.2Hashimoto, Taito; Oketani, Ryusei; Inoue, Asato; Okubo, Kohei; Oka, Kouki; Tohnai, Norimitsu; Kamiya, Kazuhide; Nakanishi, Shuji; Hisaki, Ichiro
Statically and dynamically flexible hydrogen-bonded frameworks based on 4,5,9,10-tetrakis(4-carboxyphenyl)pyrene.
Chemical communications (Cambridge, England), 2023, 59, 7224-7227
7131678 CIFC77 H56 O8P 1 21/c 17.6554; 15.342; 24.524
90; 94.763; 90
2870.4Hashimoto, Taito; Oketani, Ryusei; Inoue, Asato; Okubo, Kohei; Oka, Kouki; Tohnai, Norimitsu; Kamiya, Kazuhide; Nakanishi, Shuji; Hisaki, Ichiro
Statically and dynamically flexible hydrogen-bonded frameworks based on 4,5,9,10-tetrakis(4-carboxyphenyl)pyrene.
Chemical communications (Cambridge, England), 2023, 59, 7224-7227
7131679 CIFC22 H14 Cl N3C 1 2/c 117.4509; 12.4727; 17.6236
90; 112.121; 90
3553.6Bera, Debasish; Sarkar, Rajib; Saha, Pinaki; Ghosh, Prasanta; Mukhopadhyay, Chhanda
Aqueous mediated iodine catalyzed C-N coupling followed by C-C coupling towards 5<i>H</i>-pyrazino[2,3-<i>b</i>]indoles.
Chemical communications (Cambridge, England), 2023, 59, 7771-7774
7131680 CIFC22 H13 F2 N3P 1 21/c 19.5735; 12.6239; 28.8448
90; 93.918; 90
3477.9Bera, Debasish; Sarkar, Rajib; Saha, Pinaki; Ghosh, Prasanta; Mukhopadhyay, Chhanda
Aqueous mediated iodine catalyzed C-N coupling followed by C-C coupling towards 5<i>H</i>-pyrazino[2,3-<i>b</i>]indoles.
Chemical communications (Cambridge, England), 2023, 59, 7771-7774
7131681 CIFC43 H38 Cl2 F12 N4P 21 21 219.681; 10.2423; 10.6706
90; 90; 90
2150.97Patra, Ashoke Kumar; Srimayee, Soumya; Halder, Dibakar; Roy, Anik; Mukherjee, Souvik; Kundu, Somenath; Hossain, Maidul; Saha, Rajat; Lee, Chang-Hee; Manna, Debasis; Saha, Indrajit
Transmembrane fluoride anion transport by <i>meso</i>-3,5-bis(trifluoromethyl)phenyl picket calix[4]pyrrole.
Chemical communications (Cambridge, England), 2023, 59, 7407-7410
7131682 CIFC58 H74 F12 N5 OP n a 2121.8214; 13.2329; 20.7744
90; 90; 90
5998.8Patra, Ashoke Kumar; Srimayee, Soumya; Halder, Dibakar; Roy, Anik; Mukherjee, Souvik; Kundu, Somenath; Hossain, Maidul; Saha, Rajat; Lee, Chang-Hee; Manna, Debasis; Saha, Indrajit
Transmembrane fluoride anion transport by <i>meso</i>-3,5-bis(trifluoromethyl)phenyl picket calix[4]pyrrole.
Chemical communications (Cambridge, England), 2023, 59, 7407-7410
7131683 CIFC47 H52 Br F12 N5 OP 1 21/c 111.1101; 20.791; 21.126
90; 101.012; 90
4790Patra, Ashoke Kumar; Srimayee, Soumya; Halder, Dibakar; Roy, Anik; Mukherjee, Souvik; Kundu, Somenath; Hossain, Maidul; Saha, Rajat; Lee, Chang-Hee; Manna, Debasis; Saha, Indrajit
Transmembrane fluoride anion transport by <i>meso</i>-3,5-bis(trifluoromethyl)phenyl picket calix[4]pyrrole.
Chemical communications (Cambridge, England), 2023, 59, 7407-7410
7131684 CIFC44 H44 F12 N4 O2C 1 2/c 125.1735; 9.9028; 18.7477
90; 104.647; 90
4521.7Patra, Ashoke Kumar; Srimayee, Soumya; Halder, Dibakar; Roy, Anik; Mukherjee, Souvik; Kundu, Somenath; Hossain, Maidul; Saha, Rajat; Lee, Chang-Hee; Manna, Debasis; Saha, Indrajit
Transmembrane fluoride anion transport by <i>meso</i>-3,5-bis(trifluoromethyl)phenyl picket calix[4]pyrrole.
Chemical communications (Cambridge, England), 2023, 59, 7407-7410
7131685 CIFC91 H100 F24 I2 N10 O2P 1 21/c 111.118; 20.761; 21.874
90; 102.455; 90
4930Patra, Ashoke Kumar; Srimayee, Soumya; Halder, Dibakar; Roy, Anik; Mukherjee, Souvik; Kundu, Somenath; Hossain, Maidul; Saha, Rajat; Lee, Chang-Hee; Manna, Debasis; Saha, Indrajit
Transmembrane fluoride anion transport by <i>meso</i>-3,5-bis(trifluoromethyl)phenyl picket calix[4]pyrrole.
Chemical communications (Cambridge, England), 2023, 59, 7407-7410
7131686 CIFC58 H74 Cl F12 N5 OP n a 2121.6302; 13.5934; 20.6884
90; 90; 90
6083Patra, Ashoke Kumar; Srimayee, Soumya; Halder, Dibakar; Roy, Anik; Mukherjee, Souvik; Kundu, Somenath; Hossain, Maidul; Saha, Rajat; Lee, Chang-Hee; Manna, Debasis; Saha, Indrajit
Transmembrane fluoride anion transport by <i>meso</i>-3,5-bis(trifluoromethyl)phenyl picket calix[4]pyrrole.
Chemical communications (Cambridge, England), 2023, 59, 7407-7410
7131687 CIFC19 H15 Cl7 D Mo O2 SeP -18.2075; 12.1341; 13.2766
103.403; 90.813; 98.443
1270.7Zhang, Ming; Nian, Beifang; Wu, Zhibang; Guo, Jianhua; Chen, Zhuo; Yuan, Caifeng; Huang, Xuankun; Shen, Yiwen; Zhang, Hongbin; Tang, E.
Molybdenum(V)-mediated switching of the C(sp<sup>2</sup>)-Se bond of phenylselenyl-functionalized arenes or heterocycles under mild conditions.
Chemical communications (Cambridge, England), 2023, 59, 7599-7602
7131688 CIFC15 H7 Br O2 SeP 1 21/c 112.133; 7.2784; 14.645
90; 107.078; 90
1236.3Zhang, Ming; Nian, Beifang; Wu, Zhibang; Guo, Jianhua; Chen, Zhuo; Yuan, Caifeng; Huang, Xuankun; Shen, Yiwen; Zhang, Hongbin; Tang, E.
Molybdenum(V)-mediated switching of the C(sp<sup>2</sup>)-Se bond of phenylselenyl-functionalized arenes or heterocycles under mild conditions.
Chemical communications (Cambridge, England), 2023, 59, 7599-7602
7131689 CIFC41 H34 O12 SP 1 21 111.23; 7.3747; 23.959
90; 99.251; 90
1958.43Wu, Yuling; Zhou, Wu-Jingyun; Yao, Laiping; Niu, Yadi; Zhao, Hongli; Peng, Cheng; Han, Bo; Huang, Wei; Zhan, Gu
Organocatalytic atroposelective synthesis of naphthoquinone thioglycosides from aryl-naphthoquinones and thiosugars.
Chemical communications (Cambridge, England), 2023, 59, 7279-7282
7131690 CIFC19 H20 Cl N OP -17.564; 10.371; 11.366
109.224; 91.783; 96.951
833.3Ye, Hao; Zhu, Xi-Wei; Pan, Yi-Yun; Sun, Jie; Sun, Fei; Wu, Xin-Xing
Highly regioselective and stereoselective cascade reductive cyclization of δ-ketoamide: practical access to oxa-bridged benzazepines.
Chemical communications (Cambridge, England), 2023, 59, 7587-7590
7131691 CIFC21 H24 B N3 O6 SI -426.3367; 26.3367; 6.5069
90; 90; 90
4513.3Miyazaki, Ryuya; Muto, Kei; Yamaguchi, Junichiro
Chloroacetyl boronate <i>N</i>-tosylhydrazone as a versatile synthetic building block.
Chemical communications (Cambridge, England), 2023, 59, 7419-7422
7131692 CIFC18 H25 B Cl N3 O8 SP 1 21/c 113.2505; 15.1794; 11.4864
90; 90.823; 90
2310.07Miyazaki, Ryuya; Muto, Kei; Yamaguchi, Junichiro
Chloroacetyl boronate <i>N</i>-tosylhydrazone as a versatile synthetic building block.
Chemical communications (Cambridge, England), 2023, 59, 7419-7422
7131693 CIFC16 H13 N O2P n a 217.5072; 23.008; 7.4733
90; 90; 90
1290.8Paul, Aditya; Sengupta, Arunava; Yadav, Somnath
Visible-light driven acetoxylation and dioxygenation of indoles <i>via</i> electron donor-acceptor complexes.
Chemical communications (Cambridge, England), 2023, 59, 7455-7458
7131694 CIFC17 H14 Br N O2P 1 21/c 19.6226; 17.3895; 9.3029
90; 106.767; 90
1490.5Paul, Aditya; Sengupta, Arunava; Yadav, Somnath
Visible-light driven acetoxylation and dioxygenation of indoles <i>via</i> electron donor-acceptor complexes.
Chemical communications (Cambridge, England), 2023, 59, 7455-7458
7131695 CIFC10 H28 Cl8 N4 Zn2P 1 21 111.6505; 12.1341; 16.4837
90; 90.02; 90
2330.27Han, Xiao; Cheng, Puxin; Han, Wenqing; Shi, Rongchao; Guan, Junjie; Li, Geng; Xu, Jialiang
Circularly polarized luminescence and nonlinear optical harmonic generation based on chiral zinc halides.
Chemical communications (Cambridge, England), 2023, 59, 7447-7450
7131696 CIFC20 H56 Cl16 N8 Zn4P 1 21 111.6567; 12.1248; 16.4859
90; 90.02; 90
2330.04Han, Xiao; Cheng, Puxin; Han, Wenqing; Shi, Rongchao; Guan, Junjie; Li, Geng; Xu, Jialiang
Circularly polarized luminescence and nonlinear optical harmonic generation based on chiral zinc halides.
Chemical communications (Cambridge, England), 2023, 59, 7447-7450
7131697 CIFC77 H70 B20 Cl2 N4 O4P -115.168; 15.529; 17.352
65.517; 76.901; 82.058
3618Yang, Xiaodong; Li, Haishuang; Shao, Dong; He, Gang
Carborane based chalcogen-fused phenazines for visible light induced ATRP.
Chemical communications (Cambridge, England), 2023, 59, 7643-7646
7131698 CIFC38 H34 B10 N2 S2P -110.207; 13.006; 13.541
94.16; 90.439; 97.056
1779Yang, Xiaodong; Li, Haishuang; Shao, Dong; He, Gang
Carborane based chalcogen-fused phenazines for visible light induced ATRP.
Chemical communications (Cambridge, England), 2023, 59, 7643-7646
7131699 CIFC38 B10 N2 Se2P 1 21/n 114.546; 10.201; 24.68
90; 95.087; 90
3648Yang, Xiaodong; Li, Haishuang; Shao, Dong; He, Gang
Carborane based chalcogen-fused phenazines for visible light induced ATRP.
Chemical communications (Cambridge, England), 2023, 59, 7643-7646
7131700 CIFC30 H52 B2 Fe O2 P2P 1 21/n 19.6026; 10.9986; 29.9514
90; 94.869; 90
3151.91Grose, Laura A.; Willcox, Darren
Olefin hydroboration catalyzed by an iron-borane complex.
Chemical communications (Cambridge, England), 2023, 59, 7427-7430
7131701 CIFC25 H24 O6.03 S2P 1 21/c 17.4811; 14.9608; 20.8358
90; 93.776; 90
2326.95Reddy, Mandapati Bhargava; McGarrigle, Eoghan M.
Iodine-mediated photoinduced tuneable disulfonylation and sulfinylsulfonylation of alkynes with sodium arylsulfinates.
Chemical communications (Cambridge, England), 2023, 59, 7767-7770
7131702 CIFC16 H48 Br32 Cl N Si32P c c n13.8596; 26.555; 29.2504
90; 90; 90
10765.4Bamberg, Marcel; Gasevic, Thomas; Bolte, Michael; Virovets, Alexander; Lerner, Hans-Wolfram; Grimme, Stefan; Bursch, Markus; Wagner, Matthias
Brominated [20]silafulleranes: pushing the limits of steric loading.
Chemical communications (Cambridge, England), 2023, 59, 7459-7462
7131703 CIFC16 H36 Br44 Cl N Si32C 1 2/c 115.2828; 26.6284; 29.007
90; 91.721; 90
11799.3Bamberg, Marcel; Gasevic, Thomas; Bolte, Michael; Virovets, Alexander; Lerner, Hans-Wolfram; Grimme, Stefan; Bursch, Markus; Wagner, Matthias
Brominated [20]silafulleranes: pushing the limits of steric loading.
Chemical communications (Cambridge, England), 2023, 59, 7459-7462
7131704 CIFC369 H702 N94 O130 Zr6F m -359.677; 59.677; 59.677
90; 90; 90
212530Ortín-Rubio, Borja; Perona-Bermejo, Cristina; Suárez Del Pino, José A; Carmona, Francisco J.; Gándara, Felipe; Navarro, Jorge A. R.; Juanhuix, Judith; Imaz, Inhar; Maspoch, Daniel
A mesoporous Zr-based metal-organic framework driven by the assembly of an octatopic linker.
Chemical communications (Cambridge, England), 2023, 59, 7803-7806
7131705 CIFC18 H18 O4 SP 1 21/c 18.3144; 9.8167; 20.8013
90; 99.087; 90
1676.49Takatsuki, Masaharu; Aoyama, Hiroshi; Murai, Kenichi; Arisawa, Mitsuhiro; Sako, Makoto
Heteroannulation of bicyclobutane derivatives <i>via</i> Au-catalyzed hydration to enol ethers and intramolecular cyclization giving spirocyclobutanes.
Chemical communications (Cambridge, England), 2023, 59, 7467-7470
7131706 CIFC18 H18 O4 SP 1 21/n 111.154; 8.1794; 17.502
90; 96.951; 90
1585Takatsuki, Masaharu; Aoyama, Hiroshi; Murai, Kenichi; Arisawa, Mitsuhiro; Sako, Makoto
Heteroannulation of bicyclobutane derivatives <i>via</i> Au-catalyzed hydration to enol ethers and intramolecular cyclization giving spirocyclobutanes.
Chemical communications (Cambridge, England), 2023, 59, 7467-7470
7131707 CIFC32 H28 N2 O5P 21 21 214.925; 21.683; 24.35
90; 90; 90
2600.3Adorinni, Simone; Goti, Giulio; Rizzo, Lorenzo; Grassi, Federica; Kralj, Slavko; Matroodi, Fatima; Natali, Mirco; De Zorzi, Rita; Marchesan, Silvia; Dell'Amico, Luca
Self-assembly of benzophenone-diphenylalanine conjugate into a nanostructured photocatalyst.
Chemical communications (Cambridge, England), 2023, 59, 7619-7622
7131708 CIFC22 H23 N OI 419.4725; 19.4725; 9.2892
90; 90; 90
3522.3Li, Jiajun; Zhai, Xinyi; Ji, Cheng-Long; Li, Weipeng; Xie, Jin
Dinuclear-gold-catalyzed cyclization of 1,7-enynes with alkyl bromides.
Chemical communications (Cambridge, England), 2023, 59, 7943-7946
7131709 CIFC17 H24 N4 O6P 1 21 15.0975; 36.4142; 10.0043
90; 95.264; 90
1849.18Ma, Liulei; Zheng, Qixuan; Unruh, Daniel K.; Hutchins, Kristin M.
Reversible interconversion of pharmaceutical salt polymorphs facilitated by mechanical methods.
Chemical communications (Cambridge, England), 2023, 59, 7779-7782
7131710 CIFC17 H24 N4 O6P 15.06945; 9.75039; 19.4424
85.4911; 88.8333; 77.8317
936.51Ma, Liulei; Zheng, Qixuan; Unruh, Daniel K.; Hutchins, Kristin M.
Reversible interconversion of pharmaceutical salt polymorphs facilitated by mechanical methods.
Chemical communications (Cambridge, England), 2023, 59, 7779-7782
7131711 CIFC68 H96 N16 O24P 1 21 15.0732; 36.4013; 10.0547
90; 95.365; 90
1848.68Ma, Liulei; Zheng, Qixuan; Unruh, Daniel K.; Hutchins, Kristin M.
Reversible interconversion of pharmaceutical salt polymorphs facilitated by mechanical methods.
Chemical communications (Cambridge, England), 2023, 59, 7779-7782
7131712 CIFC17 H24 N4 O6P 15.0665; 9.7541; 19.4423
85.388; 88.841; 77.804
936.09Ma, Liulei; Zheng, Qixuan; Unruh, Daniel K.; Hutchins, Kristin M.
Reversible interconversion of pharmaceutical salt polymorphs facilitated by mechanical methods.
Chemical communications (Cambridge, England), 2023, 59, 7779-7782
7131713 CIFC22 H26 B N O6P 1 c 115.3311; 10.06926; 13.62417
90; 101.312; 90
2062.34Halford-McGuff, John M; Cordes, David B.; Watson, Allan J. B.
Synthesis of complex aryl MIDA boronates by Rh-catalyzed [2+2+2] cycloaddition.
Chemical communications (Cambridge, England), 2023, 59, 7759-7762
7131714 CIFC17 H17 N O3 SP 1 21/c 115.125; 7.7985; 12.6248
90; 95.692; 90
1481.78Halford-McGuff, John M; Cordes, David B.; Watson, Allan J. B.
Synthesis of complex aryl MIDA boronates by Rh-catalyzed [2+2+2] cycloaddition.
Chemical communications (Cambridge, England), 2023, 59, 7759-7762
7131715 CIFC17 H22 B N O6P 1 21/c 113.106; 9.9589; 13.1775
90; 91.771; 90
1719.12Halford-McGuff, John M; Cordes, David B.; Watson, Allan J. B.
Synthesis of complex aryl MIDA boronates by Rh-catalyzed [2+2+2] cycloaddition.
Chemical communications (Cambridge, England), 2023, 59, 7759-7762
7131716 CIFC43 H28 Cl14 Sb2P 1 21/n 110.6573; 34.0386; 14.0166
90; 97.905; 90
5036.34Nishiuchi, Tomohiko; Uchida, Kazuyuki; Kubo, Takashi
Synthesis and structural evaluation of closed-shell folded and open-shell twisted hexabenzo[5.6.7]quinarene.
Chemical communications (Cambridge, England), 2023, 59, 7379-7382
7131717 CIFC42 H26C 1 2/c 126.2349; 10.4272; 24.3603
90; 123.766; 90
5539.8Nishiuchi, Tomohiko; Uchida, Kazuyuki; Kubo, Takashi
Synthesis and structural evaluation of closed-shell folded and open-shell twisted hexabenzo[5.6.7]quinarene.
Chemical communications (Cambridge, England), 2023, 59, 7379-7382
7131723 CIFC18 H16 N5 OP 21 21 217.9211; 8.4929; 24.4236
90; 90; 90
1643.05Lin, Cheng-Zhou; Jiang, Ling-Feng; Zhang, Guang-Yi; Zhou, Fang-Shuai; Wu, Shao-Hua; Cao, Jing; Deng, Qing-Hai
Enantioselective synthesis of 3a-azido-pyrroloindolines by copper-catalyzed asymmetric dearomative azidation of tryptamines.
Chemical communications (Cambridge, England), 2023, 59, 7831-7834
7131724 CIFC20 H18 N O4 PP 1 21/n 111.34363; 9.78579; 15.6829
90; 93.0143; 90
1738.49Yang, Zhongzhen; Tam, Jerry K. F.; Wootton, Jack M.; Lynam, Jason M.; Unsworth, William P.
Ring expansion reactions of PO-containing molecules.
Chemical communications (Cambridge, England), 2023, 59, 7927-7930
7131725 CIFC264 H280 N24 O48C 1 2/c 128.49; 7.868; 27.678
90; 90.235; 90
6204Akhdar, Ayman; Nauton, Lionel; Jouffret, Laurent; Faure, Sophie; Gautier, Arnaud
Cage-like structures based on constrained cyclic arylopeptoids.
Chemical communications (Cambridge, England), 2023, 59, 8087-8090
7131726 CIFC9 H30 Br5 N3 PbP 21 21 218.6172; 11.8062; 21.5472
90; 90; 90
2192.13Ru, Hua-Yang; Wang, Zhao-Yang; Liu, Hua-Li; Zang, Shuang-Quan
Regulating structural asymmetry <i>via</i> fluorination engineering in hybrid lead bromide perovskites.
Chemical communications (Cambridge, England), 2023, 59, 8111-8114
7131727 CIFC6 H14 Br4 F6 N2 PbP 2 21 217.9087; 8.9042; 24.2405
90; 90; 90
1707.03Ru, Hua-Yang; Wang, Zhao-Yang; Liu, Hua-Li; Zang, Shuang-Quan
Regulating structural asymmetry <i>via</i> fluorination engineering in hybrid lead bromide perovskites.
Chemical communications (Cambridge, England), 2023, 59, 8111-8114
7131728 CIFC6 H14 Br4 F6 N2 PbP 21 21 224.248; 8.90729; 7.91028
90; 90; 90
1708.49Ru, Hua-Yang; Wang, Zhao-Yang; Liu, Hua-Li; Zang, Shuang-Quan
Regulating structural asymmetry <i>via</i> fluorination engineering in hybrid lead bromide perovskites.
Chemical communications (Cambridge, England), 2023, 59, 8111-8114
7131729 CIFC22 H45 Li N4 SiP 1 21/n 19.8325; 15.373; 17.1794
90; 93.668; 90
2591.43Barker, Jordan; Davison, Nathan; Waddell, Paul G.; Lu, Erli
Monomeric lithium and sodium silylbenzyl complexes: syntheses, structures, and CO bond olefination.
Chemical communications (Cambridge, England), 2023, 59, 8083-8086
7131730 CIFC22 H45 N4 Na SiP 1 21/c 114.0881; 9.606; 20.0799
90; 102.389; 90
2654.14Barker, Jordan; Davison, Nathan; Waddell, Paul G.; Lu, Erli
Monomeric lithium and sodium silylbenzyl complexes: syntheses, structures, and CO bond olefination.
Chemical communications (Cambridge, England), 2023, 59, 8083-8086
7131731 CIFC37 H42 Cl2 Cu2 F12 N8 O2 P2P -111.014; 14.2677; 15.3705
84.99; 75.303; 67.883
2164.4Pal, Nilay Kumar; Patra, Moumita; Pandey, Prabhakar K.; Bera, Jitendra K.
Hydroarylation of alkynes <i>via</i> dual <i>ortho</i>-C-H functionalization of diaryl amines on a dicopper(I,I) platform.
Chemical communications (Cambridge, England), 2023, 59, 8079-8082
7131732 CIFC34 H28 N2P -110.7845; 11.1594; 11.3909
72.04; 88.325; 68.64
1209.1Pal, Nilay Kumar; Patra, Moumita; Pandey, Prabhakar K.; Bera, Jitendra K.
Hydroarylation of alkynes <i>via</i> dual <i>ortho</i>-C-H functionalization of diaryl amines on a dicopper(I,I) platform.
Chemical communications (Cambridge, England), 2023, 59, 8079-8082
7131733 CIFC21 H17 Br NP n m a8.0166; 13.4004; 15.2143
90; 90; 90
1634.41Pal, Nilay Kumar; Patra, Moumita; Pandey, Prabhakar K.; Bera, Jitendra K.
Hydroarylation of alkynes <i>via</i> dual <i>ortho</i>-C-H functionalization of diaryl amines on a dicopper(I,I) platform.
Chemical communications (Cambridge, England), 2023, 59, 8079-8082
7131734 CIFC73 H104 Mg4 N4 O4C 1 2/c 118.6792; 26.1398; 15.8494
90; 112.9; 90
7128.9Seifert, Fabian; Görls, Helmar; Kupfer, Stephan; Kretschmer, Robert
A tetranuclear magnesium hydride cluster with a four-coordinate hydride in near square-planar geometry.
Chemical communications (Cambridge, England), 2023, 59, 7627-7630
7131735 CIFC66 H96 Mg4 N4 O4P -18.6237; 16.238; 23.7002
104.51; 97.671; 91.644
3177.49Seifert, Fabian; Görls, Helmar; Kupfer, Stephan; Kretschmer, Robert
A tetranuclear magnesium hydride cluster with a four-coordinate hydride in near square-planar geometry.
Chemical communications (Cambridge, England), 2023, 59, 7627-7630
7131736 CIFC30 H28 O3P 18.022; 8.2914; 10.1712
76.898; 85.404; 62.195
582.577Cieśliński, Adam; Frankowski, Sebastian; Albrecht, Łukasz
Pentaenolate activation in the organocatalytic allylic alkylation of indene-2-carbaldehydes.
Chemical communications (Cambridge, England), 2023, 59, 7655-7658
7131737 CIFC117 H121 N5 O18 Si8P -113.215; 13.961; 32.976
80.96; 81.34; 65.17
5428.6Grzelczak, Rafał A; Władyczyn, Anna; Białońska, Agata; John, Łukasz; Szyszko, Bartosz
POSSaxanes: active-template synthesis of organic-inorganic rotaxanes incorporating cubic silsesquioxane stoppers.
Chemical communications (Cambridge, England), 2023, 59, 7579-7582
7131738 CIFC95 H133 N5 O17 Si8P -114.151; 15.072; 46.449
89.53; 84.35; 87.5
9849Grzelczak, Rafał A; Władyczyn, Anna; Białońska, Agata; John, Łukasz; Szyszko, Bartosz
POSSaxanes: active-template synthesis of organic-inorganic rotaxanes incorporating cubic silsesquioxane stoppers.
Chemical communications (Cambridge, England), 2023, 59, 7579-7582
7131745 CIFC15 H22 N2 O7P 21 21 218.24888; 8.64551; 24.3498
90; 90; 90
1736.52Chen, Yun-Xuan; Han, Tian-Jiao; Xiao, Xiao; Wang, Min-Can; Mei, Guang-Jian
Catalytic asymmetric interrupted Attanasi reaction: access to fused 2,3-dihydropyrroles with vicinal quaternary carbons.
Chemical communications (Cambridge, England), 2023, 59, 8103-8106
7131746 CIFC32 H48 N4 O14P -19.4928; 9.8026; 11.3802
102.528; 110.036; 102.007
924.02Chen, Yun-Xuan; Han, Tian-Jiao; Xiao, Xiao; Wang, Min-Can; Mei, Guang-Jian
Catalytic asymmetric interrupted Attanasi reaction: access to fused 2,3-dihydropyrroles with vicinal quaternary carbons.
Chemical communications (Cambridge, England), 2023, 59, 8103-8106
7131757 CIFC17 H21 N3 SP 1 21/c 118.5673; 5.8814; 15.1443
90; 99.72; 90
1630.04Hensinger, Magenta J.; Closs, Anna C.; Trapp, Oliver; Ofial, Armin R.
The effect of <i>S</i>-alkylation on organocatalytic enamine activation through imidazolidine-4-thiones.
Chemical communications (Cambridge, England), 2023, 59, 8091-8094
7131782 CIFC21 H21 F3 Ir N3 O5 SP -17.824; 10.972; 14.212
95.459; 94.385; 98.09
1197.4Zhang, Long; Lu, Zhiyao; Rander, Andrew R.; Williams, Travis J.
An ambient pressure, direct hydrogenation of ketones.
Chemical communications (Cambridge, England), 2023, 59, 8107-8110
7131783 CIFC19 H19 Cl Ir N3 OP 1 21/c 18.718; 15.1641; 14.4976
90; 106.108; 90
1841.35Zhang, Long; Lu, Zhiyao; Rander, Andrew R.; Williams, Travis J.
An ambient pressure, direct hydrogenation of ketones.
Chemical communications (Cambridge, England), 2023, 59, 8107-8110
7131792 CIFC24 H17 Cl N2 O SeP 1 21/c 120.765; 14.171; 15.154
90; 109.346; 90
4207.4Zhou, Yunhao; Zheng, Tao; Xu, Yue; Li, Bo; Wang, Yuchi; Mei, Ruhuai; Gu, Linghui; Ma, Wenbo
Palladium-catalyzed distal selective C-H chalcogenation of biphenyl amines.
Chemical communications (Cambridge, England), 2023, 59, 8262-8265
7131793 CIFC24 H18 N2 O SeP 1 21/n 115.2884; 12.8941; 21.3671
90; 106.412; 90
4040.5Zhou, Yunhao; Zheng, Tao; Xu, Yue; Li, Bo; Wang, Yuchi; Mei, Ruhuai; Gu, Linghui; Ma, Wenbo
Palladium-catalyzed distal selective C-H chalcogenation of biphenyl amines.
Chemical communications (Cambridge, England), 2023, 59, 8262-8265
7131794 CIFC22 H15 N SeP b c a8.3047; 18.4642; 21.707
90; 90; 90
3328.54Zhou, Yunhao; Zheng, Tao; Xu, Yue; Li, Bo; Wang, Yuchi; Mei, Ruhuai; Gu, Linghui; Ma, Wenbo
Palladium-catalyzed distal selective C-H chalcogenation of biphenyl amines.
Chemical communications (Cambridge, England), 2023, 59, 8262-8265
7131795 CIFC21 H24 Br N3 O2P c a 2116.8943; 9.1586; 13.1298
90; 90; 90
2031.55Karjee, Pallab; Mandal, Santu; Debnath, Bijoy; Namdev, Nirali; Punniyamurthy, Tharmalingam
Expedient (3+3)-annulation of <i>in situ</i> generated azaoxyallyl cations with diaziridines.
Chemical communications (Cambridge, England), 2023, 59, 8270-8273
7131796 CIFC30 H31 N3 O5P 21 21 211.3754; 21.9762; 11.2116
90; 90; 90
2802.77Ruan, Peiran; Zhang, Cefei; Wu, Jin; Xiao, Fengnan; Zhang, Yongyan; Tan, Qingfa; Su, Zhishan; Feng, Xiaoming; Liu, Xiaohua
Asymmetric [3+2]-cyclization of α-imino amide surrogates to construct 3,4-diaminopyrrolidine-2,5-diones.
Chemical communications (Cambridge, England), 2023, 59, 8250-8253
7131797 CIFC210 H155 La N12 O11 Pd2P -330.9679; 30.9679; 34.1539
90; 90; 120
28365.8Sudan, Sylvain; Fadaei-Tirani, Farzaneh; Severin, Kay
A five-stranded heterometallic helicate.
Chemical communications (Cambridge, England), 2023, 59, 8258-8261
7131798 CIFC14 H36 I4 N2 SnP b c a9.2171; 8.5923; 34.046
90; 90; 90
2696.3Singh, Akash; Crace, Ethan; Xie, Yi; Mitzi, David B.
A two-dimensional lead-free hybrid perovskite semiconductor with reduced melting temperature.
Chemical communications (Cambridge, England), 2023, 59, 8302-8305
7131799 CIFC14 H36 I4 N2 SnP b c a9.04641; 8.47695; 34.0759
90; 90; 90
2613.14Singh, Akash; Crace, Ethan; Xie, Yi; Mitzi, David B.
A two-dimensional lead-free hybrid perovskite semiconductor with reduced melting temperature.
Chemical communications (Cambridge, England), 2023, 59, 8302-8305
7131800 CIFC20 H15 N O4 SP 1 21/c 115.1494; 15.0265; 7.6701
90; 101.096; 90
1713.4Kagami, Kentaro; Liang, Xueying; Ishibashi, Nanako; Ohrui, Sayaka; Tayu, Masanori; Saito, Nozomi
Synthesis of <i>N</i>-(acyloxy)-<i>N</i>-alkynylamides <i>via</i> generation of "C<sub>2</sub>" from hypervalent alkynyliodane and a weak base.
Chemical communications (Cambridge, England), 2023, 59, 8274-8277
7131814 CIFC62 H86 Cl4 F6 Ga2 N4 O6 S2 Sb2C 1 2/c 127.5361; 15.2489; 21.8879
90; 126.335; 90
7403.7Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131815 CIFC134 H118 B2 F48 Ga2 N4 Sb2P 1 21/c 113.6688; 18.938; 26.072
90; 91.6077; 90
6746.3Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131816 CIFC73 H102 Bi F3 Ga2 N8 O3 SP 1 21/n 112.803; 27.401; 26.932
90; 97.813; 90
9360.4Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131817 CIFC30 H42 F3 Ga N2 O3 SP 1 21/m 18.9025; 19.9339; 9.8991
90; 116.469; 90
1572.56Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131818 CIFC78 H110 Cl8 F6 Ga2 N8 O6 S2 Sb2P -112.454; 13.829; 14.985
103.273; 93.858; 110.942
2314.1Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131819 CIFC60 H82 Bi F6 Ga2 N4 O6 S2C 1 2/c 121.384; 12.297; 25.544
90; 102.543; 90
6557Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131820 CIFC78 H110 Bi2 Cl8 F6 Ga2 N8 O6 S2P -112.4333; 13.8507; 14.937
102.794; 93.662; 110.684
2318.1Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131821 CIFC118 H90 B2 F44 Ga2 N4 Sb2P -114.5284; 14.8141; 15.7805
66.932; 67.28; 74.7
2856.9Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131822 CIFC134 H118 B2 Bi2 F48 Ga2 N4P 1 21/c 113.615; 19.075; 26.067
90; 91.714; 90
6766.7Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131823 CIFC118 H90 B2 Bi2 F44 Ga2 N4P -114.5343; 14.8399; 15.7735
67.1304; 67.4082; 75.032
2870.32Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131824 CIFC72 H92 Bi2 F8 Ga2 N4 O6 S2C 1 2/c 127.988; 15.4048; 22.156
90; 127.475; 90
7581.1Weinert, Hanns M.; Schulte, Yannick; Gehlhaar, Alexander; Wölper, Christoph; Haberhauer, Gebhard; Schulz, Stephan
Metal-coordinated distibene and dibismuthene dications - isoelectronic analogues of butadiene dications.
Chemical communications (Cambridge, England), 2023, 59, 7755-7758
7131825 CIFC15 H31 Br O3 SiP 1 21 113.5084; 8.3024; 26.1715
90; 102.594; 90
2864.57Hikawa, Ryoga; Shimogaki, Mio; Kano, Taichi
Construction of three contiguous stereocenters through amine-catalyzed asymmetric aldol reactions.
Chemical communications (Cambridge, England), 2023, 59, 8424-8427
7131826 CIFC11 H19 N O3P 1 21/c 111.3947; 8.8485; 12.0913
90; 107.819; 90
1160.63Mazloomi, Zahra; Kallmeier, Fabian; Kirchhecker, Sarah; Stadler, Bernhard M.; Pandey, Swechchha; Schünemann, Claas; Spannenberg, Anke; Hering-Junghans, Christian; Tin, Sergey; de Vries, Johannes G.; Baráth, Eszter
Unusual selectivity in the ring-opening of γ-valerolactone oxide by amines.
Chemical communications (Cambridge, England), 2023, 59, 8444-8447
7131828 CIFC14 H9 N3 SP 1 21/n 17.5144; 8.8611; 17.9123
90; 101.248; 90
1169.8Zhao, Yu-Qiang; Zhu, Liping; Lu, Jian-Mei; Yu, Le; Zhang, Lanyun; Zhou, Ying
New charge transfer-based organic room temperature phosphorescent trace doping systems.
Chemical communications (Cambridge, England), 2023, 59, 8396-8399
7131829 CIFC14 H9 F3 N2 SP 1 21/c 112.0962; 9.1516; 11.7094
90; 97.352; 90
1285.6Zhao, Yu-Qiang; Zhu, Liping; Lu, Jian-Mei; Yu, Le; Zhang, Lanyun; Zhou, Ying
New charge transfer-based organic room temperature phosphorescent trace doping systems.
Chemical communications (Cambridge, England), 2023, 59, 8396-8399
7131830 CIFC15 H8 F6 N2 SP -18.5804; 9.4893; 10.4129
102.43; 109.29; 107.08
717.67Zhao, Yu-Qiang; Zhu, Liping; Lu, Jian-Mei; Yu, Le; Zhang, Lanyun; Zhou, Ying
New charge transfer-based organic room temperature phosphorescent trace doping systems.
Chemical communications (Cambridge, England), 2023, 59, 8396-8399
7131831 CIFC14 H10 Br2 N4 S2P n a 2117.2218; 4.0384; 22.4366
90; 90; 90
1560.43Zhao, Yu-Qiang; Zhu, Liping; Lu, Jian-Mei; Yu, Le; Zhang, Lanyun; Zhou, Ying
New charge transfer-based organic room temperature phosphorescent trace doping systems.
Chemical communications (Cambridge, England), 2023, 59, 8396-8399
7131832 CIFC25 H17 N3 SP 1 21/n 110.7111; 8.8354; 21.003
90; 101.75; 90
1946.01Zhao, Yu-Qiang; Zhu, Liping; Lu, Jian-Mei; Yu, Le; Zhang, Lanyun; Zhou, Ying
New charge transfer-based organic room temperature phosphorescent trace doping systems.
Chemical communications (Cambridge, England), 2023, 59, 8396-8399
7131833 CIFC25 H19 N3 SP 1 21/c 117.3606; 10.3859; 11.4467
90; 97.743; 90
2045.1Zhao, Yu-Qiang; Zhu, Liping; Lu, Jian-Mei; Yu, Le; Zhang, Lanyun; Zhou, Ying
New charge transfer-based organic room temperature phosphorescent trace doping systems.
Chemical communications (Cambridge, England), 2023, 59, 8396-8399
7131834 CIFC22 H20 B Fe NP 1 21/c 113.616; 11.0195; 11.277
90; 91.301; 90
1691.6Schneider, Johannes S.; Krummenacher, Ivo; Braunschweig, Holger; Helten, Holger
Linear and macrocyclic oligo(<i>p</i>-phenylene iminoboranes) with ferrocenyl side groups - observation of selective, non-templated macrocyclization.
Chemical communications (Cambridge, England), 2023, 59, 8408-8411
7131835 CIFC38 H34 B2 Fe2 N2P -110.3432; 12.985; 13.579
102.62; 111.269; 107.505
1506.7Schneider, Johannes S.; Krummenacher, Ivo; Braunschweig, Holger; Helten, Holger
Linear and macrocyclic oligo(<i>p</i>-phenylene iminoboranes) with ferrocenyl side groups - observation of selective, non-templated macrocyclization.
Chemical communications (Cambridge, England), 2023, 59, 8408-8411
7131836 CIFC68 H64 B4 Cl8 Fe4 N4C 1 2/c 122.807; 20.081; 15.326
90; 114.023; 90
6411Schneider, Johannes S.; Krummenacher, Ivo; Braunschweig, Holger; Helten, Holger
Linear and macrocyclic oligo(<i>p</i>-phenylene iminoboranes) with ferrocenyl side groups - observation of selective, non-templated macrocyclization.
Chemical communications (Cambridge, England), 2023, 59, 8408-8411
7131837 CIFC16 H14 B Br FeP 1 21/c 18.92; 11.581; 13.82
90; 100.5; 90
1403.7Schneider, Johannes S.; Krummenacher, Ivo; Braunschweig, Holger; Helten, Holger
Linear and macrocyclic oligo(<i>p</i>-phenylene iminoboranes) with ferrocenyl side groups - observation of selective, non-templated macrocyclization.
Chemical communications (Cambridge, England), 2023, 59, 8408-8411
7131842 CIFC117 H165 Al2 N8P -111.973; 12.393; 20.373
99.341; 93.667; 113.676
2703.8Balayan, Kajal; Sharma, Himanshu; Vanka, Kumar; Ravindranathan, Sapna; Gonnade, Rajesh G.; Sen, Sakya S.
On the competition between six-membered and five-membered NHC towards alane centered ring expansion.
Chemical communications (Cambridge, England), 2023, 59, 8540-8543
7131843 CIFC28 H40 Al Br3 N2P 1 21/c 121.7906; 17.5474; 17.0364
90; 111.758; 90
6050.1Balayan, Kajal; Sharma, Himanshu; Vanka, Kumar; Ravindranathan, Sapna; Gonnade, Rajesh G.; Sen, Sakya S.
On the competition between six-membered and five-membered NHC towards alane centered ring expansion.
Chemical communications (Cambridge, England), 2023, 59, 8540-8543
7131844 CIFC29 H42 Al F3 N2 O3 SP 21 21 2110.812; 16.198; 17.618
90; 90; 90
3085Balayan, Kajal; Sharma, Himanshu; Vanka, Kumar; Ravindranathan, Sapna; Gonnade, Rajesh G.; Sen, Sakya S.
On the competition between six-membered and five-membered NHC towards alane centered ring expansion.
Chemical communications (Cambridge, England), 2023, 59, 8540-8543
7131845 CIFC32 H33 N3 O6 SP -19.8721; 10.9778; 15.0003
111.083; 96.959; 94.009
1494.3Zheng, Jianfeng; Bi, Jingzhi; Ma, Lan; Chen, Lvli; Tang, Luhao; Xiong, Dong; Tian, Yin
Metal-free anomalous [5+1] cycloaddition reactions of donor-acceptor aziridines for the synthesis of 2<i>H</i>-1,4-oxazines.
Chemical communications (Cambridge, England), 2023, 59, 8572-8575
7131846 CIFC32 H33 N3 O6 SP 1 21/n 18.253; 28.894; 13.2728
90; 107.124; 90
3024.8Zheng, Jianfeng; Bi, Jingzhi; Ma, Lan; Chen, Lvli; Tang, Luhao; Xiong, Dong; Tian, Yin
Metal-free anomalous [5+1] cycloaddition reactions of donor-acceptor aziridines for the synthesis of 2<i>H</i>-1,4-oxazines.
Chemical communications (Cambridge, England), 2023, 59, 8572-8575
7131852 CIFC66 H90 Cr2 N4 P2P -112.8677; 13.10453; 18.2132
99.9375; 90.7104; 92.7071
3021.09Elsayed Moussa, M.; Rummel, E.-M.; Balázs, G; Riesinger, C.; Noor, A.; Kempe, R.; Scheer, M.
Unusual coordination mode for 1,3-diphosphete ligands towards a Cr-Cr quintuple bond complex.
Chemical communications (Cambridge, England), 2023, 59, 8588-8591
7131853 CIFC61 H73 Cr2 N4 PP 1 2/c 110.2784; 22.2038; 12.5344
90; 105.268; 90
2759.6Elsayed Moussa, M.; Rummel, E.-M.; Balázs, G; Riesinger, C.; Noor, A.; Kempe, R.; Scheer, M.
Unusual coordination mode for 1,3-diphosphete ligands towards a Cr-Cr quintuple bond complex.
Chemical communications (Cambridge, England), 2023, 59, 8588-8591
7131854 CIFC17 H16 N2 O2P 1 21/c 110.2278; 8.9747; 15.8181
90; 106.584; 90
1391.6Reddy, Chada Raji; Ganesh, Veeramalla; Punna, Nagender
Aminative annulation of cyano-enynyl esters leading to functionalized cyclopentenones.
Chemical communications (Cambridge, England), 2023, 59, 8600-8603
7131855 CIFC38 H32 Br2 N2 S2P -19.382; 10.472; 17.945
88.563; 78.673; 72.965
1651.9Muthusamy, Sengodagounder; Naveen, Ramasamy; Kumar, Muniyappankovilthottam Devaraj Senthil
Base-mediated cascade synthesis of indole diolefins: a route to spiro[cyclopentene-indole]thiones and thiepino[2,3-<i>b</i>]indoles.
Chemical communications (Cambridge, England), 2023, 59, 8560-8563
7131884 CIFC36 H29 F12 N OP b c a20.2437; 9.7698; 33.781
90; 90; 90
6681.1Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131885 CIFC72 H93 Cl4 N2 O2 Os PP -111.6271; 15.7458; 20.984
101.733; 101.092; 107.493
3452.8Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131886 CIFC52 H74 Cl2 N2 O2 RuP 1 21/c 117.1927; 22.2351; 13.901
90; 100.305; 90
5228.4Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131887 CIFC72 H58 Cl2 F24 N2 O2 RuP -113.2962; 13.5768; 21.676
76.1839; 82.2455; 68.8954
3539.7Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131888 CIFC52 H74 Cl2 N2 O2 RuP 1 21/c 118.8219; 12.0482; 22.0868
90; 92.6706; 90
5003.2Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131889 CIFC72 H93 Cl4 N2 O2 P RuP -111.6411; 15.7348; 20.953
101.789; 101.156; 107.309
3451.5Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131890 CIFC52 H74 Cl2 N2 O2 OsP 1 21/c 117.3519; 22.294; 13.7682
90; 100.358; 90
5239.3Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131891 CIFC52 H74 Cl2 N2 O2 OsP 1 21/c 118.7953; 12.0376; 22.148
90; 92.0871; 90
5007.7Ayson, Patricia Rose H.; Brown, Seth N.
Slip to π Ru: structural distortions due to metal-iminoxolene π bonding.
Chemical communications (Cambridge, England), 2023, 59, 9618-9621
7131900 CIFC5 H7 N3P b c n21.861; 6.7837; 7.501
90; 90; 90
1112.4Rastogi, Gaurav K.; Deb, Mohit L.; Baruah, Pranjal K.
Copper-catalysed dehydrogenative self-coupling/cyclization of 5-aminopyrazoles: synthesis and photophysical study of pyridazines.
Chemical communications (Cambridge, England), 2023, 59, 9642-9645
7131909 CIFC22 H17 N O2P 1 21/n 18.549; 9.093; 20.815
90; 96.522; 90
1607.6Roy, Shantonu; Karmakar, Sudip; Mondal, Imtiaj; Naskar, Koushik; Sarkar, Writhabrata; Deb, Indubhusan
Electrochemical C(sp<sup>3</sup>)-C(sp<sup>3</sup>) cross-dehydrogenative coupling: enabling access to 9-substituted fluorescent acridanes.
Chemical communications (Cambridge, England), 2023, 59, 9074-9077
7131910 CIFC24 H21 N O3P 1 21/n 113.5269; 9.3422; 15.1324
90; 105.484; 90
1842.9Roy, Shantonu; Karmakar, Sudip; Mondal, Imtiaj; Naskar, Koushik; Sarkar, Writhabrata; Deb, Indubhusan
Electrochemical C(sp<sup>3</sup>)-C(sp<sup>3</sup>) cross-dehydrogenative coupling: enabling access to 9-substituted fluorescent acridanes.
Chemical communications (Cambridge, England), 2023, 59, 9074-9077
7132293 CIFC27 H22 N2 O2 SP 1 21 19.3277; 26.9016; 9.3909
90; 107.691; 90
2245.02Dyguda, Mateusz; Przydacz, Artur; Albrecht, Łukasz
Dearomative, aminocatalytic formal normal-electron-demand aza-Diels-Alder cycloaddition in the synthesis of tetrahydrofuropyridines.
Chemical communications (Cambridge, England), 2023, 59, 12903-12906
7132294 CIFC40 H45 N O2 WP 1 21/n 113.2327; 18.0672; 14.089
90; 97.292; 90
3341.12Yadav, Rinku; Ghiviriga, Ion; Abboud, Khalil K.; Veige, Adam S.
A case of alkylidyne-imine metathesis.
Chemical communications (Cambridge, England), 2023, 59, 12899-12902
7132295 CIFC45 H49 N O2 WP -19.425; 12.4; 16.608
95.897; 92.628; 103.096
1875.7Yadav, Rinku; Ghiviriga, Ion; Abboud, Khalil K.; Veige, Adam S.
A case of alkylidyne-imine metathesis.
Chemical communications (Cambridge, England), 2023, 59, 12899-12902
7132296 CIFC44 H47 N O2 WP -19.3557; 11.8178; 16.8483
101.459; 91.875; 99.739
1795.12Yadav, Rinku; Ghiviriga, Ion; Abboud, Khalil K.; Veige, Adam S.
A case of alkylidyne-imine metathesis.
Chemical communications (Cambridge, England), 2023, 59, 12899-12902
7132297 CIFC39 H45 N O2 WC 1 2/c 123.9026; 11.1201; 26.2556
90; 97.854; 90
6913.3Yadav, Rinku; Ghiviriga, Ion; Abboud, Khalil K.; Veige, Adam S.
A case of alkylidyne-imine metathesis.
Chemical communications (Cambridge, England), 2023, 59, 12899-12902
7132298 CIFC H11 B3 F4 N4 O4C 1 2/c 115.28; 8.7593; 14.8039
90; 98.748; 90
1958.3Chen, Ziqi; Li, Fuming; Yang, Zhihua; Pan, Shilie; Mutailipu, Miriding
Hydroxyfluorooxoborate (NH<sub>4</sub>)[C(NH<sub>2</sub>)<sub>3</sub>][B<sub>3</sub>O<sub>3</sub>F<sub>4</sub>(OH)] for exploring the effects of cation substitution on structure and optical properties.
Chemical communications (Cambridge, England), 2023, 59, 12435-12438
7132299 CIFC21 H24 Cl F6 I O2P 1 21 18.94012; 12.9377; 9.96505
90; 93.8561; 90
1149.99Milzarek, Tobias M.; Ramirez, Nieves P.; Liu, Xing-Yu; Waser, Jerome
One-pot synthesis of functionalized bis(trifluoromethylated)benziodoxoles from iodine(I) precursors.
Chemical communications (Cambridge, England), 2023, 59, 12637-12640
7132422 CIFC26 H24 N2 O2P 1 21/n 112.1441; 10.4866; 21.897
90; 97.791; 90
2762.8Biswas, Subhamoy; Shit, Sudip; Behera, Bipin Kumar; Sahu, Archana Kumari; Saikia, Anil K.
Leveraging cascade alkynyl Prins cyclization towards the stereoselective synthesis of spiro-furan quinazolinone scaffolds.
Chemical communications (Cambridge, England), 2023, 59, 14301-14304

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