Crystallography Open Database

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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 54

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7122632 CIFC22 H27 N3 O5P 1 21/c 119.306; 10.033; 11.1506
90; 93.091; 90		2156.7Roy, Subhra Kanti; Tiwari, Anuj; Saleem, Mohammed; Jana, Chandan K.
Metal free direct C(sp<sup>2</sup>)-H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators.
Chemical communications (Cambridge, England), 2018, 54, 14081-14084
7122633 CIFC22 H17 N OP 21 21 2110.4148; 10.5315; 15.0526
90; 90; 90		1651Roy, Subhra Kanti; Tiwari, Anuj; Saleem, Mohammed; Jana, Chandan K.
Metal free direct C(sp<sup>2</sup>)-H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators.
Chemical communications (Cambridge, England), 2018, 54, 14081-14084
7122634 CIFC2.48 H2.07 N0.14 O0.41P b c a13.692; 9.81; 21.438
90; 90; 90		2879.5Roy, Subhra Kanti; Tiwari, Anuj; Saleem, Mohammed; Jana, Chandan K.
Metal free direct C(sp<sup>2</sup>)-H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators.
Chemical communications (Cambridge, England), 2018, 54, 14081-14084
7122635 CIFC19 H16 Br N O3P 1 21/c 111.6484; 13.0417; 11
90; 91.035; 90		1670.79Roy, Subhra Kanti; Tiwari, Anuj; Saleem, Mohammed; Jana, Chandan K.
Metal free direct C(sp<sup>2</sup>)-H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators.
Chemical communications (Cambridge, England), 2018, 54, 14081-14084
7122636 CIFC2.45 H2.19 N0.13 O0.39P 1 21/c 111.796; 11.9194; 11.1919
90; 90.881; 90		1573.4Roy, Subhra Kanti; Tiwari, Anuj; Saleem, Mohammed; Jana, Chandan K.
Metal free direct C(sp<sup>2</sup>)-H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators.
Chemical communications (Cambridge, England), 2018, 54, 14081-14084
7122637 CIFC16 H12 N2 O3P 1 21/c 15.4752; 17.649; 13.8907
90; 94.311; 90		1338.5Roy, Subhra Kanti; Tiwari, Anuj; Saleem, Mohammed; Jana, Chandan K.
Metal free direct C(sp<sup>2</sup>)-H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators.
Chemical communications (Cambridge, England), 2018, 54, 14081-14084
7122638 CIFC16 H9 N O2P 1 21/n 13.9089; 23.323; 12.35
90; 94.388; 90		1122.6Roy, Subhra Kanti; Tiwari, Anuj; Saleem, Mohammed; Jana, Chandan K.
Metal free direct C(sp<sup>2</sup>)-H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators.
Chemical communications (Cambridge, England), 2018, 54, 14081-14084
7122642 CIFC19 H42 Co N2 Si2P -110.1876; 11.4336; 11.504
114.154; 91.303; 94.57		1216.53Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122643 CIFC23 H46 Co N2P 1 21/c 119.9887; 14.6087; 18.638
90; 116.655; 90		4864.1Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122644 CIFC21 H42 Co N2P 1 21/n 115.1042; 9.823; 15.6224
90; 99.477; 90		2286.24Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122645 CIFC22 H54 Co P2 Si2C 1 2/c 115.49; 10.6608; 17.9769
90; 104.618; 90		2872.5Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122646 CIFC39 H40 Co N2C 1 2/c 117.7086; 16.5959; 12.4453
90; 120.799; 90		3141.7Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122647 CIFC40 H52 Mg2P -18.3199; 9.8137; 11.2729
69.434; 87.336; 78.887		845.38Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122648 CIFC20 H36 Co P2P b c a13.5926; 17.2078; 17.6656
90; 90; 90		4132Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122649 CIFC21 H46 Co N2 Si2P 1 21/n 115.4002; 9.5019; 17.5196
90; 90.785; 90		2563.42Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122650 CIFC20 H38 Co N2 O2 SiP 1 21/c 111.7966; 9.3515; 21.2898
90; 95.121; 90		2339.23Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122651 CIFC26 H40 Co N2 O2P -110.6538; 11.3442; 11.9505
100.249; 109.396; 101.338		1288.75Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122652 CIFC31 H46 Co N2P 1 21/c 111.8818; 20.2773; 11.9197
90; 91.93; 90		2870.19Enachi, Andreea; Baabe, Dirk; Zaretzke, Marc-Kevin; Schweyen, Peter; Freytag, Matthias; Raeder, Jan; Walter, Marc D.
[(NHC)CoR<sub>2</sub>]: pre-catalysts for homogeneous olefin and alkyne hydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 13798-13801
7122653 CIFC16 H22 N O6 P WP 1 21/c 19.6668; 16.0328; 12.9821
90; 96.27; 90		2000.01Fassbender, Jan; Schnakenburg, Gregor; Gates, Derek P.; Espinosa Ferao, Arturo; Streubel, Rainer
Unconventional ionic ring-deconstruction pathways of a three-membered heterocycle.
Chemical communications (Cambridge, England), 2018, 54, 14013-14016
7124471 CIFC36 H38 Br2 N4 O4P -19.5585; 11.0081; 16.9501
84.171; 85.069; 70.438		1669.3Wang, Hongyu; Man, Yunquan; Wang, Kaiye; Wan, Xiuyan; Tong, Lili; Li, Na; Tang, Bo
Hydrogen bond directed aerobic oxidation of amines via photoredox catalysis.
Chemical communications (Cambridge, England), 2018, 54, 10989-10992
7124472 CIFC14 H34 B2 N4P n a 2120.751; 14.369; 5.958
90; 90; 90		1776.5Ramos, Alberto; Antiñolo, Antonio; Carrillo-Hermosilla, Fernando; Fernández-Galán, Rafael; Rodríguez-Diéguez, Antonio; García-Vivó, Daniel
Carbodiimides as catalysts for the reduction of CO<sub>2</sub> with boranes.
Chemical communications (Cambridge, England), 2018, 54, 4700-4703
7124473 CIFC16 H29 B N2 O2P -111.49; 12.061; 12.206
89.223; 86.315; 81.499		1669.5Ramos, Alberto; Antiñolo, Antonio; Carrillo-Hermosilla, Fernando; Fernández-Galán, Rafael; Rodríguez-Diéguez, Antonio; García-Vivó, Daniel
Carbodiimides as catalysts for the reduction of CO<sub>2</sub> with boranes.
Chemical communications (Cambridge, England), 2018, 54, 4700-4703
7124474 CIFC23 H44 B2 N2P -19.8852; 15.1771; 16.6307
69.154; 84.904; 79.674		2293.1Ramos, Alberto; Antiñolo, Antonio; Carrillo-Hermosilla, Fernando; Fernández-Galán, Rafael; Rodríguez-Diéguez, Antonio; García-Vivó, Daniel
Carbodiimides as catalysts for the reduction of CO<sub>2</sub> with boranes.
Chemical communications (Cambridge, England), 2018, 54, 4700-4703
7124475 CIFC16 H31 B N2 OP 1 21/c 111.825; 18.6367; 19.5807
90; 126.909; 90		3450.4Ramos, Alberto; Antiñolo, Antonio; Carrillo-Hermosilla, Fernando; Fernández-Galán, Rafael; Rodríguez-Diéguez, Antonio; García-Vivó, Daniel
Carbodiimides as catalysts for the reduction of CO<sub>2</sub> with boranes.
Chemical communications (Cambridge, England), 2018, 54, 4700-4703
7124476 CIFC42.75 H56.5 B2 Cl1.5 Mo2 N12 O4 PP -110.6555; 12.0934; 21.6561
84.805; 77.532; 67.728		2521.42Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7124477 CIFC41 H55 B2 Cl2 N12 O4 P W2P 1 21/n 111.4608; 19.9952; 21.5347
90; 91.254; 90		4933.7Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7124478 CIFC42 H49 As B2 Mo2 N12 O4P -111.5185; 13.0665; 17.5152
92.37; 100.329; 108.935		2439.02Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7124479 CIFC42 H49 As B2 N12 O4 W2P -111.5217; 13.0117; 17.5872
92.152; 100.361; 109.048		2438.44Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7124480 CIFC40 H53 As B2 N12 O4 W2P -110.756; 29.5247; 32.3562
68.469; 86.621; 85.103		9519.1Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7124483 CIFC64 H96 Mg2 N4P -111.6151; 12.8269; 13.1163
76.087; 74.884; 67.493		1721Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7124484 CIFC53 H43 B F20 N2P 1 21/n 110.73722; 32.4655; 14.61307
90; 100.97; 90		5000.87Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7124486 CIFC50 H60 Cl N5P 1 21 110.1635; 20.791; 10.5547
90; 102.641; 90		2176.2Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7124487 CIFC48 H54 N4 O3P 1 21/c 116.8622; 9.5715; 26.4871
90; 90.972; 90		4274.3Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7124488 CIFC22 H21 N O3 S2P 21 21 217.9445; 10.19612; 25.8377
90; 90; 90		2092.93Li, Jin-Shan; Liu, Yong-Jie; Li, Shen; Ma, Jun-An
Chiral phosphoric acid-catalyzed direct asymmetric mannich reaction of cyclic C-acylimines with simple ketones: facile access to C2-quaternary indolin-3-ones.
Chemical communications (Cambridge, England), 2018, 54, 9151-9154
7124489 CIFC4 H4 Br2 Cu N4 O2 PtC m m m7.3275; 10.5863; 7.1618
90; 90; 90		555.549Sergeenko, Ania S.; Ovens, Jeffrey S.; Leznoff, Daniel B.
Designing anisotropic cyanometallate coordination polymers with unidirectional thermal expansion (TE): 2D zero and 1D colossal positive TE.
Chemical communications (Cambridge, England), 2018, 54, 1599-1602
7124490 CIFC4 Cl2 Cu N4 O2 PtC m m m7.2595; 10.1348; 7.249
90; 90; 90		533.33Sergeenko, Ania S.; Ovens, Jeffrey S.; Leznoff, Daniel B.
Designing anisotropic cyanometallate coordination polymers with unidirectional thermal expansion (TE): 2D zero and 1D colossal positive TE.
Chemical communications (Cambridge, England), 2018, 54, 1599-1602
7124491 CIFC46 H58 Cl2 F12 N4 P2 Rh2P -18.2841; 11.8607; 25.557
95.308; 94.332; 93.372		2487.7Lionetti, Davide; Day, Victor W.; Lassalle-Kaiser, Benedikt; Blakemore, James D.
Multiple binding modes of an unconjugated bis(pyridine) ligand stabilize low-valent [Cp*Rh] complexes.
Chemical communications (Cambridge, England), 2018, 54, 1694-1697
7124492 CIFC23.33 H29 F6 N2 P RhP -110.68; 11.8136; 11.8896
117.254; 108.438; 97.3701		1196.94Lionetti, Davide; Day, Victor W.; Lassalle-Kaiser, Benedikt; Blakemore, James D.
Multiple binding modes of an unconjugated bis(pyridine) ligand stabilize low-valent [Cp*Rh] complexes.
Chemical communications (Cambridge, England), 2018, 54, 1694-1697
7124493 CIFC23 H29 N2 RhP 1 21/c 110.8564; 11.6907; 16.6402
90; 103.578; 90		2052.93Lionetti, Davide; Day, Victor W.; Lassalle-Kaiser, Benedikt; Blakemore, James D.
Multiple binding modes of an unconjugated bis(pyridine) ligand stabilize low-valent [Cp*Rh] complexes.
Chemical communications (Cambridge, England), 2018, 54, 1694-1697
7124494 CIFC22 H15 F N2 O2P -19.1885; 9.6792; 11.035
64.897; 78.682; 89.685		868.09Roy, Subhasish; Pradhan, Sourav; Punniyamurthy, Tharmalingam
Copper-mediated regioselective C-H etherification of naphthylamides with arylboronic acids using water as an oxygen source.
Chemical communications (Cambridge, England), 2018, 54, 3899-3902
7124495 CIFC9 H6 F N O3 SP -15.682; 7.9839; 11.5941
70.6; 77.45; 86.006		484.24Leng, Jing; Qin, Hua-Li
1-Bromoethene-1-sulfonyl fluoride (1-Br-ESF), a new SuFEx clickable reagent, and its application for regioselective construction of 5-sulfonylfluoro isoxazoles.
Chemical communications (Cambridge, England), 2018, 54, 4477-4480
7124496 CIFC27 H35 O12 S3 Ti3P -110.2226; 13.5319; 13.5794
105.493; 99.264; 107.574		1664.9Liu, Gang; Yang, Xing; Bonnefont, Antoine; Lv, Yaokang; Chen, Jun; Dan, Wenyan; Chen, Zuofeng; Ruhlmann, Laurent; Wright, Dominic S.; Zhang, Cheng
Conjugated hybrid films based on a new polyoxotitanate monomer.
Chemical communications (Cambridge, England), 2018, 54, 14132-14135
7124497 CIFC41 H40 Cl2 N10 O4C 1 2/c 127.5324; 9.3673; 19.5352
90; 128.892; 90		3921.4Sawant, Devesh M.; Sharma, Shivani; Pathare, Ramdas S.; Joshi, Gaurav; Kalra, Sourav; Sukanya, Sukanya; Maurya, Antim K.; Metre, Ramesh K.; Agnihotri, Vijai K.; Khan, Shahnawaz; Kumar, Raj; Pardasani, R. T.
Relay tricyclic Pd(ii)/Ag(i) catalysis: design of a four-component reaction driven by nitrene-transfer on isocyanide yields inhibitors of EGFR.
Chemical communications (Cambridge, England), 2018, 54, 11530-11533
7125318 CIFC96 H108 N12P 61 2 223.3698; 23.3698; 89.848
90; 90; 120		42496Zhang, Pei; Wang, Xinchang; Xuan, Wei; Peng, Pixian; Li, Zhihao; Lu, Ruqiang; Wu, Shuang; Tian, Zhongqun; Cao, Xiaoyu
Chiral separation and characterization of triazatruxene-based face-rotating polyhedra: the role of non-covalent facial interactions.
Chemical communications (Cambridge, England), 2018, 54, 4685-4688
7125319 CIFC96 H108 N12P 65 2 223.3854; 23.3854; 89.444
90; 90; 120		42362Zhang, Pei; Wang, Xinchang; Xuan, Wei; Peng, Pixian; Li, Zhihao; Lu, Ruqiang; Wu, Shuang; Tian, Zhongqun; Cao, Xiaoyu
Chiral separation and characterization of triazatruxene-based face-rotating polyhedra: the role of non-covalent facial interactions.
Chemical communications (Cambridge, England), 2018, 54, 4685-4688
7125320 CIFC9 H6 Cl0.25 N2 O5 Tb0.5F m -3 c54.8796; 54.8796; 54.8796
90; 90; 90		165285Du, Wei; Zhu, Zhifeng; Bai, Yue-Ling; Yang, Zhen; Zhu, Shourong; Xu, Jiaqiang; Xie, Zhaoxiong; Fang, Jianhui
An anionic sod-type terbium-MOF with extra-large cavities for effective anthocyanin extraction and methyl viologen detection.
Chemical communications (Cambridge, England), 2018, 54, 5972-5975
7125321 CIFC36 H41 B N O PP 1 21/n 110.0854; 17.8383; 16.192
90; 96.009; 90		2897Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125322 CIFC66 H80 B2 N2 P2 PtP b c n16.708; 22.4099; 16.7415
90; 90; 90		6268.4Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125323 CIFC40 H57 B Br3 Co N2 PP 1 21/n 113.563; 16.1347; 18.638
90; 95.679; 90		4058.6Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125324 CIFC32 H33 B N P SeP c a 2117.601; 17.365; 17.358
90; 90; 90		5305.3Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125325 CIFC32 H37 B N PP 1 21/c 118.893; 15.0154; 20.461
90; 114.845; 90		5267.3Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125326 CIFC40 H57 B Br3 Fe N2 PP 1 21/n 113.5457; 16.1351; 18.6839
90; 95.303; 90		4066.1Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125327 CIFC70 H93 B2 Br Co N8 P2C m c e25.9634; 17.706; 29.773
90; 90; 90		13686.9Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125328 CIFC144 H168 B4 Br4 Co3 N6 O6 P4P 1 21/c 122.776; 11.6346; 27.261
90; 113.332; 90		6633.2Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125329 CIFC16 H12 N2 O2P -17.0483; 12.691; 14.4533
103.668; 90.921; 102.65		1222.6Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125330 CIFC19 H21 F N2 O2P -16.3592; 9.7262; 15.058
92.739; 99.147; 106.484		877.5Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125331 CIFC20 H20 N2 O3P 1 21/n 19.8482; 12.1953; 15.5327
90; 106.98; 90		1784.18Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125332 CIFC20 H23 F N2 O2P 1 21/c 111.9347; 13.0246; 12.4263
90; 112.805; 90		1780.61Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125333 CIFC32 H30 N4 O3P -110.711; 11.136; 13.512
100.641; 104.19; 113.52		1358.4Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125334 CIFC16 H16 N2 OP -111.1136; 11.2993; 12.7113
105.175; 101.292; 114.625		1313.2Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125335 CIFC17 H14 N2 O2 SP 1 21/c 17.1819; 12.909; 16.108
90; 99.316; 90		1473.7Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125336 CIFC21 H22 N2 O3I 1 2/a 113.1564; 14.1743; 20.5373
90; 93.892; 90		3821Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125337 CIFC19 H18 N2 O3P 1 21/n 19.0284; 12.6694; 14.298
90; 96.266; 90		1625.7Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125338 CIFC20 H14 N2P 1 21/c 17.0181; 7.9004; 25.5706
90; 92.661; 90		1416.25Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125339 CIFC16 H14 N2 OP 21 21 215.729; 14.295; 15.456
90; 90; 90		1265.8Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125340 CIFC121 H200 N6 O4 Si4 Y2P 1 2/c 123.3487; 12.1983; 21.8684
90; 92.992; 90		6219.9Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125341 CIFC99 H176 N6 O4 Si4 Yb2P -110.9326; 12.067; 21.041
105.472; 96.265; 94.586		2641.9Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125342 CIFC107 H182 N6 O4 Si4 Yb2P 1 2/c 121.5295; 12.1512; 23.1374
90; 93.7523; 90		6040Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125343 CIFC44 H60 N2 O2I 1 2/c 113.5259; 9.785; 29.268
90; 95.506; 90		3855.8Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125344 CIFC44 H72 N2 O2P -19.6188; 9.9837; 12.2473
101.903; 98.362; 113.312		1022.59Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125345 CIFC50 H76 N3 O2 Si2 YP 1 21/c 115.3478; 16.3591; 20.5634
90; 94.045; 90		5150.1Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125346 CIFC46 H84 N3 O2 Si2 YP -110.8751; 12.0478; 20.872
105.371; 96.234; 94.373		2605.5Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125347 CIFC50 H76 N3 O2 Si2 YbP 1 21/c 115.212; 16.174; 20.7742
90; 95.218; 90		5090.1Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125348 CIFC14 H19 Cd Cl N9 PP 21 21 2110.7129; 12.186; 16.3333
90; 90; 90		2132.27Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125349 CIFC14 H18 Cd F N9 PC 1 2/c 118.909; 10.618; 10.507
90; 111.75; 90		1959.4Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125350 CIFC14 H19 Cd Cl N9 PP b c n16.65; 16.667; 15.809
90; 90; 90		4387Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125351 CIFC14 H18 Cd F N9 PC m c e16.172; 15.6943; 16.8867
90; 90; 90		4286Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125352 CIFC24 H20 S4P 1 21/n 17.1311; 8.3942; 17.2693
90; 95.931; 90		1028.2Phan, Ngoc-Minh; Zakharov, Lev N.; Johnson, Darren W.
Copper(ii) serves as an efficient additive for metal-directed self-assembly of over 20 thiacyclophanes.
Chemical communications (Cambridge, England), 2018, 54, 13419-13422
7125353 CIFC24 H20 S4A e a 210.8663; 8.5571; 22.5617
90; 90; 90		2097.88Phan, Ngoc-Minh; Zakharov, Lev N.; Johnson, Darren W.
Copper(ii) serves as an efficient additive for metal-directed self-assembly of over 20 thiacyclophanes.
Chemical communications (Cambridge, England), 2018, 54, 13419-13422
7125456 CIFC24 H18 Cl N O2P 1 21/n 110.9587; 7.7456; 22.4121
90; 100.151; 90		1872.6Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866
7125457 CIFC21 H15 N O2 SP n a 2110.0386; 16.6863; 10.3764
90; 90; 90		1738.1Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866
7125458 CIFC20 H13 N O2P 1 21/c 112.115; 16.3598; 7.7826
90; 108.183; 90		1465.5Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866

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