子结构搜索

90467

CCOC(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CCCC4)cc3)cc2N=C(N)C1
Reaction #66262
(1E,4E)-ethyl 2-amino-8-(4-(pyrrolidine-1-carbonyl)phenyl)-3H-benzo[b]azepine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C=CCC#N)cc1
Reaction #76405
4-p-tolyl-but-3-enenitrile
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C=CC(C#N)=NO)cc1
Reaction #76406
2-Hydroxyimino-4-p-tolyl-but-3-enenitrile
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C=CC(C#N)=NOS(C)(=O)=O)cc1
Reaction #76407
2-methanesulfonyloxyimino-4-p-tolyl-but-3-enenitrile
收率 64.3%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC=Cc1ccc(Cc2ccc(C=CCC#N)cc2)cc1
Reaction #76414
4-{4-[4-(3-cyano-propenyl)-benzyl]-phenyl}-but-3-enenitrile
收率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(C=Cc1ccc(Cc2ccc(C=CC(C#N)=NO)cc2)cc1)=NO
Reaction #76415
4-{4-[4-(3-cyano-3-hydroxyimino-propenyl)-benzyl]-phenyl}-2-hydroxyimino-but-3-enenitrile
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/CC#N)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157716
title compound
收率 53.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/Cc2nc(=O)o[nH]2)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157887
3-[(2E)-3-(4-tert-butylphenyl)-3-(5-chloro-6-methoxypyridin-2-yl)prop-2-en-1-yl]-1,2,4-oxadiazol-5(2H)-one
收率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1c(Cc2ccccc2)c(O)c(C2=C(C(C)(C)C(N)=O)CCC(C)C2)c(O)c1Cc1ccccc1
Reaction #460009
2-[2-(1-Aminocarbonyl-1-methylethyl)-5-methyl-1-cyclohexenyl]-5-(1,1-dimethylheptyl)dibenzylresorcinol
DOI: 10.6084/m9.figshare.5104873.v1
CCC/C(C#N)=C1/c2ccc(CO)cc2COc2ccccc21
Reaction #539380
(E)-2-(8-hydroxymethyl-6,11-dihydrodibenzo[b,e]oxepin-11-ylidene)pentanenitrile
收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CCCC4)cc3)cc2N=C(N)C1
Reaction #680607
(1E,4E)-ethyl 2-amino-8-(4-(pyrrolidine-1-carbonyl)phenyl)-3H-benzo[b]azepine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=Cc2ccc(C(F)(F)C(F)(F)F)cc2N=C(N)C1
Reaction #1045417
DOI: 10.1039/C8SC04228D
CS[C@H]1O[C@@H](c2ccc(C)c(Cc3ccc(/C=C/CC#N)cc3)c2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #1586483
adduct 28
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=Cc2ccc(C(F)(F)C(F)(F)F)cc2N=C(N)C1
Reaction #1776909
(1E,4E)-ethyl 2-amino-8-(perfluoroethyl)-3H-benzo[b]azepine-4-carboxylate
收率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=Cc2ccc(C(F)(F)C(F)(F)F)cc2N=C(N)C1
Reaction #1960679
(1E,4E)-ethyl 2-amino-8-(perfluoroethyl)-3H-benzo[b]azepine-4-carboxylate
收率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1cc(OCc2ccccc2)c(C2=C(C(C)(C)C(N)=O)CCC(C)C2)c(OCc2ccccc2)c1
Reaction #2239337
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=Cc2ccc(-c3ccc(C(=O)N4CCCC4)cc3)cc2N=C(N)C1
Reaction #2413637
DOI: 10.1039/C8SC04228D