Поиск подструктуры

COc1cccc(N)c1

COc1cccc(N2CCCC2c2cc(C(=O)N(C)C)cc3c(=O)cc(N4CCOCC4)oc23)c1
Reaction #497
Выход 27.5%
COC(=O)c1cc(C2CCCN2c2cccc(OC)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #570
Выход 55.5%
O=C(Nc1ccc2c(c1)OCO2)c1ccc([N+](=O)[O-])cc1
Reaction #2542
title compound
Выход 87.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4cnccn4)nc3cc2Oc2ccccc2F)cn1
Reaction #41574
5-(2-Fluoro-phenoxy)-2-pyrazin-2-yl-6-(6-methanesulfonyl-pyridin-3-oxy)-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4cc[nH]n4)nc3cc2Oc2ccccc2F)cn1
Reaction #41575
compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(-c2nc3cc(Oc4ccccc4F)c(Oc4ccc(S(C)(=O)=O)nc4)cc3[nH]2)n1
Reaction #41576
compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc(N)c(N)cc2Oc2ccccc2Cl)cn1
Reaction #41577
4-(2-chlorophenoxy)-5-(6-methanesulfonyl-pyridin-3-yloxy)-benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4ccccn4)nc3cc2Oc2ccccc2Cl)cn1
Reaction #41578
compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2cc3[nH]c(-c4cnccn4)nc3cc2Oc2ccccc2Cl)cn1
Reaction #41579
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)CC=C(c2ccc(OC)cc2[N+](=O)[O-])CC1
Reaction #60419
1-(4,4-Diethylcyclohex-1-enyl)-4-methoxy-2-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)CC=C(c2ccc(OC)cc2N)CC1
Reaction #60420
title compound
Выход 120.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=Cc1c(C(C)=O)cc(OCc2ccccc2)cc1[N+](=O)[O-]
Reaction #61657
methyl 3-(2-acetyl-4-benzyloxy-6-nitro-phenyl)-acrylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(OCc2ccccc2)cc2c1CCC(=O)N2
Reaction #61658
5-acetyl-7-benzyloxy-3,4-dihydro-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1O)N=C(c1ccccc1F)CC2=O
Reaction #66912
43
Выход 61.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N2CCC[C@@H]2c2cc(C(=O)O)cc3c(=O)cc(N4CCOCC4)oc23)c1
Reaction #69477
8-[(2R)-(1-(3-methoxyphenyl)pyrrolidin-2-yl)]-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid
Выход 74.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCC(N(C)C)CC2)ccc1[N+](=O)[O-]
Reaction #70545
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2nn[nH]n2)cc(OCc2ccccc2)c1OCc1ccccc1
Reaction #70941
5-(3,4-bis-benzyloxy-5-nitro-phenyl)-2H-tetrazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])c(C(=O)OCc2ccccc2)cc1OCc1ccccc1
Reaction #89918
benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])c(C(=O)O)cc1OCc1ccccc1
Reaction #89919
5-(benzyloxy)-4-methoxy-2-nitrobenzoic acid
Выход 94.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2nn[nH]n2)cc(OCc2ccccc2)c1OCc1ccccc1
Reaction #90286
5-(3,4-bis-benzyloxy-5-nitrophenyl)-2H-tetrazole
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее