Поиск подструктуры

228397

COc1cc(/C=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC
Reaction #2993
intended compound
Выход 50.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)P(=O)(OCC)C(CC#N)c1ccc(Cl)cc1
Reaction #5269
ethyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccccc1NCC=Cc1ccc(Cl)cc1
Reaction #5830
title compound
Выход 82.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncccc1NCC=Cc1ccc(Cl)cc1
Reaction #5831
title compound
Выход 42.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N)c(NCC=Cc2ccc(Cl)cc2)c1
Reaction #5833
title compound
Выход 63.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(C(=O)O)c(=O)n(CC=Cc3ccc(Cl)cc3)n2)ccc1F
Reaction #8083
title compound
Выход 86.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8084
needles
Выход 17.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2nn(CC=Cc3ccc(Cl)cc3)c(=O)c(N3CCN(C(=O)OC(C)(C)C)CC3)c2C)ccc1F
Reaction #8085
title compound
Выход 87.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(OC)c(F)c2)nn(CC=Cc2ccc(Cl)cc2)c1=O
Reaction #8129
title compound
Выход 51.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C(=O)c1ccc(Cl)cc1Cl)c1ccc(Cl)cc1
Reaction #8876
crude product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccc(Cl)cc2)c(-c2ccc(Cl)cc2Cl)[nH]c1=O
Reaction #8877
6-(2,4-Dichlorophenyl)-5-(4-chlorophenyl)-2-oxo-1,2-dihydropyridine-3-nitrile
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C(=O)c1ccc(Cl)cc1Cl)c1ccc(Cl)cc1
Reaction #42077
crude product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccc(Cl)cc2)c(-c2ccc(Cl)cc2Cl)[nH]c1=O
Reaction #42078
6-(2,4-Dichlorophenyl)-5-(4-chlorophenyl)-2-oxo-1,2-dihydropyridine-3-nitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(NC(C)=O)c2cc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)nc2n(C)c1=O
Reaction #42119
N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-methoxy-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1c(C=C2C(=O)Nc3cc(Cl)ccc32)[nH]c2c1CCCC2
Reaction #52784
3-[2-(6-chloro-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-4,5,6,7-tetrahydro-1H-indol-3-yl]-propionic acid
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(c1ccccc1)C1CCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CC1
Reaction #73483
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1-c1ccc(C(=CN(C)C(C)c2ccccc2)c2ccc(Cl)cc2)cn1
Reaction #73809
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNCC(c1ccccc1)c1ccc(-c2cn[nH]c2)nc1
Reaction #73810
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(Cl)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75667
Compound 35
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(Cl)cc2)c2cc(Cl)ccc2N1
Reaction #75685
Compound 53
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее