Teilstruktursuche

9613

Cc1nn(-c2ccnc(Nc3ccc4c(c3)c(Cl)c(C)n4C)n2)cc1CN1CC(O)C1
Reaction #599
Ausbeute 0.0%
Cc1nn(-c2ccnc(Nc3ccc4c(c3)c(Cl)c(C)n4C)n2)cc1C=O
Reaction #628
Ausbeute 64.6%
Cn1ccc2cc(Nc3ccncc3)ccc21
Reaction #5987
solid
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(c1ccncc1)c1ccc2c(ccn2C)c1
Reaction #5988
solid
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2C)C(=O)NC3=O
Reaction #11262
( 922 )
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)O)c2cc([N+](=O)[O-])ccc2n1Cc1ccccc1
Reaction #44907
1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acid
Ausbeute 101.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)NCc2ccc(F)c(F)c2)c2cc(N)ccc2n1Cc1ccccc1
Reaction #44908
5-amino-1-benzyl-2-methyl-1H-indole-3-carboxylic acid, 3,4-difluorobenzylamide
Ausbeute 104.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc2c(c1)c(C(=O)NCc1ccc(F)c(F)c1)c(C)n2Cc1ccccc1
Reaction #44909
5-acetamido-1-benzyl-2-methyl-1H-indole-3-carboxylic acid, 3,4-difluorobenzylamide
Ausbeute 68.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc3c(ccn3C(=O)OC(C)(C)C)c2)CC1
Reaction #49268
1-(tert-butoxycarbonyl)-5-(4-methylpiperazino)indole
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2cc(Nc3ccncc3)ccc21
Reaction #49836
solid
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(c1ccncc1)c1ccc2c(ccn2C)c1
Reaction #49837
solid
Ausbeute 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)OCC)n1ccc2cc(N)ccc21
Reaction #52267
title compound
Ausbeute 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)OCC)n1ccc2cc(NC(=O)Cc3ccc4c(n3)NCCC4)ccc21
Reaction #52268
title compound
Ausbeute 68.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCc1ccc([N+](=O)[O-])cc1)C1Cc2c(ccc3c2ccn3C(=O)C2Cc3c(ccc4[nH]ccc34)N2)N1
Reaction #76240
2-(4-Nitrophenyl)ethyl 3-(pyrrolo[4,5-e]indolin-7-ylcarbonyl)pyrrolo[4,5-e]indoline-7-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c2c(c3cc([N+](=O)[O-])ccc31)CCCC2
Reaction #78883
N-isopropyl-6-nitro-1,2,3,4-tetrahydrocarbazole
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c2c(c3cc(N)ccc31)CCCC2
Reaction #78884
N-isopropyl-6-amino-1,2,3,4-tetrahydrocarbazole
Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c2c(c3cc([N+](=O)[O-])ccc31)CCCC2
Reaction #78894
N-isopropyl-6-nitro-1,2,3,4-tetrahydrocarbazole
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c2c(c3cc(N)ccc31)CCCC2
Reaction #78895
N-isopropyl-6-amino-1,2,3,4-tetrahydrocarbazole
Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2cc(N3CCN(Cc4c[nH]c5ncccc45)CC3)ccc21
Reaction #82491
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-n2cc(C#N)c3ccc(NS(C)(=O)=O)cc32)cc1
Reaction #160548
title compound
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter