Teilstruktursuche

442

CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1C(C)C
Reaction #773
Ausbeute 10.3%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #790
Ausbeute 23.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #791
Ausbeute 11.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #792
Ausbeute 3.5%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #832
Ausbeute 7.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #833
Ausbeute 0.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #834
Ausbeute 8.7%
CC(=O)N1CC(C)(C)c2ccc([N+](=O)[O-])cc21
Reaction #47922
1-(3,3-dimethyl-6-nitroindolin-1-yl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc(N)cc21
Reaction #47923
solid
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc(Nc3ncnc4c3CN(c3ncccc3Cl)CC4)cc21
Reaction #47924
solid
Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CNc2cc(Nc3ncnc4c3CN(c3ncccc3Cl)CC4)ccc21.Cl
Reaction #47925
HCl
Ausbeute 236.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCCC(C)(C)c2ccc([N+](=O)[O-])cc21
Reaction #161231
1-(5,5-dimethyl-8-nitro-2,3,4,5-tetrahydrobenzo[b]azepin-1-yl)ethanone
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCCC(C)(C)c2ccc(N)cc21
Reaction #161232
1-(8-amino-2,3,4,5-tetrahydro-5,5-dimethylbenzo[b]azepin-1-yl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc([N+](=O)[O-])cc21
Reaction #161238
1-(3,3-dimethyl-6-nitroindolin-1-yl)ethanone
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc(N)cc21
Reaction #161239
1-(6-amino-3,3-dimethyl-2,3-dihydro-indol-1-yl)-ethanone
Ausbeute 70.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(N)cc1NC(=O)c1c[nH]c2ccccc2c1=O
Reaction #161283
N-(5-amino-2-tert-butyl-phenyl)-4-oxo-1H-quinoline-3-carboxamide
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc2c3c(cc([N+](=O)[O-])c2c1)N(C(=O)c1cc2cc(OCCO)ccc2[nH]1)CC3CCl
Reaction #173714
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc2c(c1)NC(=O)CC2(C)C
Reaction #175239
DOI: 10.1039/C8SC04228D
CNC(=O)c1cccc(F)c1Nc1nc(Nc2ccc3c(c2)NC(=O)C(NC(=O)C(F)(F)F)CC3(C)C)ncc1Cl
Reaction #175289
DOI: 10.1039/C8SC04228D
C#CCNC(=O)c1cccc(F)c1Nc1nc(Nc2ccc3c(c2)NC(=O)C(NC(=O)N2CCCC2)CC3(C)C)ncc1Cl
Reaction #179521
DOI: 10.1039/C8SC04228D
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