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15064

Cc1ccc2cc3n(c2n1)[C@H](C)CN(C(=O)OC(C)(C)C)C3
Reaction #12011
desired product
Выход 71.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)cc(CO)c1
Reaction #42381
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)cc(CO)c1
Reaction #42400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1c(F)cnc2cc(F)c(OC)nc12
Reaction #43412
3,7-Difluoro-8-(1-methylethenyl)-2-(methyloxy)-1,5-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc2c(nn1)OCCC2
Reaction #43428
product
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc2c(nn1)SCCO2
Reaction #43432
solid
Выход 71.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc2c(nn1)OCC2
Reaction #43457
3-Ethenyl-5,6-dihydrofuro[2,3-c]pyridazine
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc2c(c1)C(=O)NCC2
Reaction #43633
product
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(F)cc(C)cc1[N+](=O)[O-]
Reaction #45563
compound
Выход 73.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(F)c(-c2ccccc2)c(C)c1C#N
Reaction #45803
5-Amino-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cccc(C(=O)O)c1
Reaction #49223
title compound
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc2c1C(=O)NC2
Reaction #49467
7-aminoisoindolinone
Выход 96.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cc3cc(C=O)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49472
4-methyl-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49495
4-vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(-c2cc3cc(CN4CCN(CCO[Si](C)(C)C(C)(C)C)CC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49499
4-vinyl-7-{1-(tert-butoxycarbonyl)-5-[4-(2-tert-butyldimethylsilyloxyethyl)pyperazin-1-ylmethyl]indol-2-yl}isoindolinone
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c(c1Cl)CNC2=O
Reaction #49588
4-chloro-5-vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C(=O)OC(C)(C)C)CC2)c(C2CC(C)(C)CC(C)(C)C2)c1
Reaction #60464
title compound
Выход 71.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cc2c1c(C)c(C)n2C(C)C
Reaction #70728
methyl 6-chloro-1-isopropyl-2,3-dimethyl-1H-indole-4-carboxylate
Выход 81.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)ccc1S(=O)(=O)N1CCN(C(=O)OC(C)(C)C)[C@@H](C)C1
Reaction #71658
1,1-dimethylethyl (2S)-2-methyl-4-{[2-methyl-4-(trifluoromethyl)phenyl]sulfonyl}-1-piperazinecarboxylate
Выход 90.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(F)(F)F)cc1S(=O)(=O)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #71662
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
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