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CS(=O)(=O)O.Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ccn1
Reaction #42065
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(NC(=O)C1CC(=O)N(c2cccc(NC(=O)NCc3ccccc3)c2)C1)c1cccnc1)NS(=O)(=O)c1ccccc1
Reaction #51170
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(Cl)cc([N+](=O)[O-])c1O
Reaction #58136
N-(5-chloro-2-hydroxy-3-nitrophenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)cc([N+](=O)[O-])c1O
Reaction #58137
6-amino-4-chloro-2-nitrophenol
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Oc2ccccc2)cc1
Reaction #64551
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc2c(c1)N(c1cccc[n+]1[O-])CC(C)(C)O2
Reaction #65389
2-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazin-4-yl)pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Nc1cc([N+](=O)[O-])ccc1C#CC(C)C
Reaction #68396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc2ccc([N+](=O)[O-])cc2[nH]1
Reaction #68397
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N(C)c1c([N+](=O)[O-])ccc2c1CCCN2
Reaction #76517
[Methyl(1,2,3,4-tetrahydro-6-nitro-5-quinolinyl)-amino]oxo-acetic acid ethyl ester
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(=O)[nH]c2ccc3c(c21)CCCN3
Reaction #76518
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1c([N+](=O)[O-])cc(Br)c2c1CCCN2
Reaction #76519
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cc(N2CCN(C(C)=O)CC2)ccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1
Reaction #86473
title compound
Ausbeute 15.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cc(N2CCNCC2)ccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1
Reaction #86483
title compound
Ausbeute 94.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cc(N2CCN(CCN)CC2)ccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1
Reaction #86488
title compound
Ausbeute 136.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(Nc3cc(N(C)C(=O)Nc4c(Cl)c(OC)cc(OC)c4Cl)ncn3)c(NC(=O)/C=C\Cl)c2)CC1
Reaction #86493
title compound
Ausbeute 59.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(-n2cccc2)cc([N+](=O)[O-])c1
Reaction #92386
N-(3-Nitro-5-pyrrol-1-yl-phenyl)-acetamide
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(N)cc(-n2cccc2)c1
Reaction #92387
N-(3-Amino-5-pyrrol-1-yl-phenyl)-acetamide
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(Nc2ccc(I)cc2[N+](=O)[O-])cc(-n2cccc2)c1
Reaction #92392
N-(3-(4-iodo-2-nitrophenylamino)-5-(1H-pyrrol-1-yl)phenyl)acetamide
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(Nc2ccc(Br)cc2[N+](=O)[O-])cc(-c2ccccc2)c1
Reaction #92410
N-(5-(4-bromo-2-nitrophenylamino)biphenyl-3-yl)acetamide
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(-c2ccc(F)c(F)c2)cc([N+](=O)[O-])c1
Reaction #92413
N-(3′,4′-difluoro-5-nitrobiphenyl-3-yl)acetamide
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
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