部分構造検索

257762

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
COc1cc(C(O)(C(F)(F)F)C(F)(F)F)ccc1C=CC(=O)O
Reaction #4847
3-{2 -methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acid
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(O)(C(F)(F)F)C(F)(F)F)ccc1CCC(=O)O
Reaction #4848
2-methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzenepropanoic acid
収率 80.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C=Cc1ccc(C2CCCCC2)c(Cl)c1
Reaction #54840
3-chloro-4-cyclohexylcinnamic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=Cc1ccc(C2CCCCC2)c(Cl)c1
Reaction #54841
ethyl 3-chloro-4cyclohexylcinnamate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCN(CC1(c2ccc(CC(OCC)C(=O)OC)cc2)CC1)C(=O)OC(C)(C)C
Reaction #76085
3-(4-{1-[(tert-butoxycarbonyl-heptyl-amino)-methyl]-cyclopropyl}-phenyl)-2-ethoxy-propionic acid methyl ester
収率 87.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/C(=O)O)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157710
title compound
収率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/Br)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157711
title compound
収率 25.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/C(=O)N2CCCC2)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157883
(2E)-3-(4-tert-butylphenyl)-3-(5-chloro-6-methoxypyridin-2-yl)-1-(pyrrolidin-1-yl)prop-2-en-1-one
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1=Cc2ccc(C3CC3)cc2OC1C(F)(F)F
Reaction #175062
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(c2ccc(C(C)(C)C)cc2O[SiH](C)C)c2ccccc2C1=O
Reaction #189265
DOI: 10.1039/C8SC04228D
CCOC(=O)CCc1ccc(C2COc3c(C)c(C)c(NC(=O)CC(C)(C)C)c(C)c32)cc1
Reaction #192974
DOI: 10.1039/C8SC04228D
CCOc1c(C(C)=C(F)CO)cc2c(c1Br)C(C)(C)CC=C2C(C)C
Reaction #193094
DOI: 10.1039/C8SC04228D
CC(C)(CNC(=O)c1ccc(Cl)cc1)c1cc2c(cc1Cl)C=C(C(=O)O)C(C(F)(F)F)O2
Reaction #211956
DOI: 10.1039/C8SC04228D
CCOc1cc2c(cc1C(C)=C(F)CO)C(C(C)(C)C)=CCC2(C)C
Reaction #223257
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(C)c1ccc(C2(O)CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #226048
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=Cc2cc(Cl)c(C(C)(C)CO)cc2OC1C(F)(F)F
Reaction #233940
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(C)c1ccc2c(c1)C(C)(C)CCC2(C)C
Reaction #235109
DOI: 10.1039/C8SC04228D
Cn1cnc(-c2ccc(NC(=C3C(=O)Oc4ccccc43)c3ccc(C(C)(C)N)cc3)cc2)c1
Reaction #243569
DOI: 10.1039/C8SC04228D
C=Cc1cc(CNC(=O)C=Cc2ccc(C(C)(C)C)cc2)c(OC)cc1NS(C)(=O)=O
Reaction #244540
DOI: 10.1039/C8SC04228D
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