بحث البنية الفرعية

1167533

CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52570
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52571
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
المردود 44.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(Cl)C(=O)Nc3ccc(Cl)cc32)c1OC
Reaction #59625
expected product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(Cl)C(=O)Nc2cc(C)c(Cl)cc21
Reaction #59633
expected product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc([N+](=O)[O-])ccc1N1CCOCC1
Reaction #60927
title compound
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2Cl)CC1
Reaction #60936
[4-(2-Chloro-phenyl)-piperazin-1-yl]-(2-morpholin-4-yl-5-nitro-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(Cl)c1
Reaction #60941
3-Chloro-4-[4-(2-morpholin-4-yl-5-nitro-benzoyl)-piperazin-1-yl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(F)c1
Reaction #60973
Title compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(C(F)(F)F)cc2Cl)CC1
Reaction #60982
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(OC(F)(F)F)cc2)CC1
Reaction #60984
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C(F)(F)F)ccc1N1CCN(C(=O)c2cc([N+](=O)[O-])ccc2N2CCOCC2)CC1
Reaction #60985
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #60987
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(Cl)cc2)CC1
Reaction #60995
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2F)CC1
Reaction #61007
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2Cl)CC1
Reaction #61009
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #61018
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)C(C(=O)c2ccc(S(C)(=O)=O)cc2[N+](=O)[O-])C(=O)C1
Reaction #64839
2-(4-methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dione
المردود 48.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NS(=O)(=O)c2ccc(Cl)cc2)c(C(=O)Cl)cc1OC
Reaction #72475
2-(4-chloro-phenylsulfonylamino)-4,5-dimethoxy-benzoyl chloride
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
ClC1=Nc2cccnc2Nc2ccccc21
Reaction #72505
6-chloro-11H-benzo[e]pyrido[3,2-b][1,4]diazepine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #72507
solid
المردود 74.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي