部分構造検索

COC(=O)CCBr

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)C1CSCCN1
Reaction #1569
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(Br)CCc1ccccc1
Reaction #2347
ethyl 4-benzyl-3-bromobutyrate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=CC(=O)O)c1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1
Reaction #4840
3-methyl-3-{4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2c(Cl)cccc2n1
Reaction #5524
desired product
収率 67.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(Br)C1C(=O)OC
Reaction #6070
title compound
収率 19.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1c(I)cc(I)cc1I)C(F)(F)C(F)(Br)C(F)(F)Br
Reaction #6407
material
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1c(I)cc(I)c(Br)c1I)C(F)(F)C(F)(Br)C(F)(F)Br
Reaction #6408
(2,4,6-triiodo-3-bromo-phenyl)-2,2,3,4,4-pentafluoro-3,4-dibromobutyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCn1cnc2ccccc21
Reaction #7222
ethyl-3-(benzimidazol-1-yl)propanoate
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(COC)C(=O)OCC
Reaction #10452
title compound
収率 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)CC(C)N1CCN(c2ccc(O)cc2)CC1
Reaction #41207
title compound
収率 59.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCN1CCC(OC(=O)Nc2ccccc2-c2ccccc2)CC1
Reaction #42135
title intermediate
収率 70.0%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
収率 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)C1CC2CCCC(C1)C2=O
Reaction #44497
title compound
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
収率 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
収率 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
Reaction #47824
titled compound
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OC
Reaction #47825
titled compound
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
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