بحث البنية الفرعية

1166167

N#Cc1cc(F)cc(-c2cc(N)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #7101
title compound
المردود 52.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c([N+](=O)[O-])c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45831
compound
المردود 90.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c(N)c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45832
compound
المردود 97.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2ccccc2)cc1[N+](=O)[O-]
Reaction #76841
title compound
المردود 71.8%DOI: 10.6084/m9.figshare.5104873.v1
N#[N+]c1ccc(-c2ccccc2)cc1[N+](=O)[O-].O=S(=O)([O-])O
Reaction #76842
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC(C)(C)c1cc(N=Nc2ccc(-c3ccccc3)cc2[N+](=O)[O-])c(O)c(-c2ccccc2)c1
Reaction #76843
title compound
المردود 25.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC(C)(C)c1cc(N=Nc2ccc(-c3ccccc3)cc2[N+](=O)[O-])c(O)c(C(C)(C)c2ccccc2)c1
Reaction #76845
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(-c2ccc(NC(=O)c3ccco3)c([N+](=O)[O-])c2)cc1[N+](=O)[O-])c1ccco1
Reaction #78026
3,3′-dinitro-4,4′-di-2-furoylamino-biphenyl
المردود 81.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2ccc(NC(=O)c3ccco3)c(N)c2)ccc1NC(=O)c1ccco1
Reaction #78027
3,3′-diamino-4,4′-di-2-furoylaminobiphenyl
المردود 23.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1CN(C(=O)Nc2cc(-c3ccc(F)cc3)ccc2[N+](=O)[O-])C1
Reaction #90983
tert-butyl((1-((4′-fluoro-4-nitro-[1,1′-biphenyl]-3-yl)carbamoyl)azetidin-3-yl)methyl)carbamate
المردود 69.7%DOI: 10.6084/m9.figshare.5104873.v1
NCC1CN(C(=O)Nc2cc(-c3ccc(F)cc3)ccc2[N+](=O)[O-])C1
Reaction #90984
3-(aminomethyl)-N-(4′-fluoro-4-nitro-[1,1′-biphenyl]-3-yl)azetidine-1-carboxamide
المردود 103.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1cccc(C2=Nc3ccc(-c4ccccc4F)cc3NC(=O)C2)c1
Reaction #173507
DOI: 10.1039/C8SC04228D
CN(C)c1cc2c(cc1-c1cccc(F)c1F)NC(=O)CC(c1cccc(-n3ccnn3)c1)=N2
Reaction #175147
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2ccccc2)cc1NC(=O)c1ccc(CCl)cc1
Reaction #179569
DOI: 10.1039/C8SC04228D
Nc1cc(S(=O)c2ccc(-c3ccc(Br)cc3)cc2)ccc1Cl
Reaction #180362
DOI: 10.1039/C8SC04228D
O=C1CC(c2cccc(-n3cnnn3)c2)=Nc2ccc(-c3ccccc3F)cc2N1
Reaction #182104
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2ccc(F)cc2F)cc1[N+](=O)[O-]
Reaction #182869
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2cccc(F)c2F)cc1[N+](=O)[O-]
Reaction #184674
DOI: 10.1039/C8SC04228D
O=C(C=CC1CCOCC1)Nc1ccc(-c2ccccc2C(F)(F)F)cc1[N+](=O)[O-]
Reaction #184700
DOI: 10.1039/C8SC04228D
Nc1cc(S(=O)c2ccccc2)ccc1Cl
Reaction #190267
DOI: 10.1039/C8SC04228D
الصفحة 1التالي