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1323520

Cc1ccc(OC(=CC(=O)c2ccc(Br)cc2)C(=O)c2ccc(Br)cc2)cc1
Reaction #887
1-(4-tolyloxyl)-1,2-bis(4-bromobenzoyl)ethylene
DOI: 10.6084/m9.figshare.5104873.v1
COC(CC(=O)c1ccc(Br)cc1)C(=O)c1ccc(Br)cc1
Reaction #889
1,2-Bis(4-bromobenzoyl)-1-methoxyethane
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1coc2c1C(=O)CCC2
Reaction #995
4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2c(Cl)cccc2n1
Reaction #5524
desired product
Выход 67.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(Br)C1C(=O)OC
Reaction #6070
title compound
Выход 19.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCn1cnc2ccccc21
Reaction #7222
ethyl-3-(benzimidazol-1-yl)propanoate
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(COC)C(=O)OCC
Reaction #10452
title compound
Выход 28.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1cnc(NS(=O)(=O)c2cccc(Cl)c2C)s1
Reaction #10464
Methyl (2{[(3-chloro-2-methylphenyl)sulfonyl]amino}-1,3-thiazol-5-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
Reaction #42135
title intermediate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N)n1
Reaction #42612
ethyl 2-amino-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(Nc2cnc(CNC(=O)OC(C)(C)C)c3c(OC)cc(OC)cc23)n1
Reaction #42928
2-[1-(tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinolin-4-ylamino]thiazole-4-carboxylic acid ethyl ester
Выход 42.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(Nc2cnc(CNC(=O)OC(C)(C)C)c3cc(OC)c(OC)cc23)n1
Reaction #42949
2-[1-(tert-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinolin-4-ylamino]thiazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCN1CCCN(Cc2ccc(OCc3ccccc3)cc2)CC1
Reaction #44791
methyl hexahydro-4-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine-1-propanoate
Выход 51.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(-c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)n1
Reaction #45768
compound
Выход 91.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Cl)cc1OC(C)C(=O)OC
Reaction #50475
desired material
Выход 102.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCN1CCN(c2cccc(C(F)(F)F)c2)CC1
Reaction #52195
3-[4-(3-trifluoromethylphenyl)-1-piperazinyl]propionic acid
Выход 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)OCC)n1ccc2cc(OCc3ccccc3)ccc21
Reaction #52276
title compound
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)OCC)n1ccc2cc(CCCc3ccc4cccnc4n3)ccc21
Reaction #52322
title product
Выход 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53345
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NC(=O)CCS1)OCO3
Reaction #53348
title compound
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1
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