بحث البنية الفرعية

Nc1ccc(O)cc1[N+](=O)[O-]

O=[N+]([O-])c1cc(O)c(O)cc1[N+](=O)[O-]
Reaction #3193
product
المردود 9869.8%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(OCC(O)CO)c(OCC(O)CO)cc1[N+](=O)[O-]
Reaction #3194
light yellow fluffy solid
المردود 67.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCCC1c1cc2c(cc1Oc1ccc(N)c(N)c1)nc(-c1ccccn1)n2COCC[Si](C)(C)C
Reaction #41549
1-(2-(6-(3,4-diamino-phenoxy)-2-pyridin-2-yl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc([N+](=O)[O-])c(N)cc2Oc2ccccc2C#N)cn1
Reaction #41570
5-(2-cyano-phenoxy)-4-(6-methanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc(N)c(N)cc2Oc2ccccc2C#N)cn1
Reaction #41571
4-(2-cyano-phenoxy)-5-(6-methanesulfonyl-pyridin-3-yloxy)-benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(F)c(OCc2ccccc2)cc1[N+](=O)[O-])c1cnccn1
Reaction #41603
compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(Oc2ccccc2F)c(OCc2ccccc2)cc1[N+](=O)[O-])c1cnccn1
Reaction #41604
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc(Oc2cc3nc(C4CCCN4)[nH]c3cc2N2CCC[C@@H]2C(C)=O)cc1
Reaction #41648
(2R)-1-(1-(6-(4-ethanesulfonyl-phenoxy)-2-pyrrolidin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-2-yl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4cnccn4)nc3cc2Oc2cc(F)ccc2F)cn1
Reaction #41652
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4cnccn4)nc3cc2Oc2c(F)cccc2C#N)cn1
Reaction #41655
5-(2-Fluoro-6-cyano-phenoxy)-2-pyrazin-2-yl-6-(6-ethanesulfonyl-pyridin-3-yloxy)-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Oc2ccc([N+](=O)[O-])c([N+](=O)[O-])c2)CC1
Reaction #48589
4-(3,4-dinitro-phenoxy)-1-methyl-piperidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)Oc1ccc(Oc2cc(Oc3cc(F)c(C(F)(F)F)c(Cl)c3)ccc2[N+](=O)[O-])cc1
Reaction #49787
title product
المردود 23.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Oc2cc(Oc3cc(F)c(C(F)(F)F)c(Cl)c3)ccc2[N+](=O)[O-])cc1
Reaction #49788
title product
المردود 25.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Nc1cc(Oc2ccc(NC)c([N+](=O)[O-])c2)ccn1
Reaction #59107
[4-(4-methylamino-3-nitro-phenoxy)-pyridin-2-yl]carbamic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1ccc(O)cc1[N+](=O)[O-].O=[N+]([O-])O
Reaction #75482
title compound
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C)c(-c2ccnc(Nc3ccc(O)c([N+](=O)[O-])c3)n2)s1
Reaction #75483
title compound
المردود 17.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82170
methyl carbamate ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc([N+](=O)[O-])c2c(c1)[C@]1(C)CCN(C)[C@@H]1N2C
Reaction #82172
(3aS-cis)-5-ethoxy-1,2,3,3a,8,8a- hexahydro-7-nitro-1,3a,8-trimethylpyrrolo[2,3-b]indole
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1ccc(N)c([N+](=O)[O-])c1
Reaction #86437
title compound
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc(NC2=NCN(C)C(N)=C2)c([N+](=O)[O-])c1
Reaction #86456
title compound
المردود 102.3%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي