Recherche de Sous-structure

1071373

COC(=O)C1(c2ccc3ocnc3c2)CC1
Reaction #67415
1-benzooxazol-5-yl-cyclopropanecarboxylic acid methyl ester
Rendement 98.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(c2ccc3ocnc3c2)CC1
Reaction #67416
1-(benzo[d]oxazol-5-yl)cyclopropanecarboxylic acid
Rendement 11.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1cccc(OCCN(C)C)c1)C(C)=O
Reaction #73499
methyl 2-{3-[2-(dimethylamino)ethoxy]benzyl}-3-oxobutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)(c1ccc(F)c(F)c1)c1ccc(F)c(F)c1
Reaction #77451
Ethyl 3,3′,4,4′-tetrafluorobenzilate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)CCC2CC=CC=C2N1C(=O)C(F)(F)F
Reaction #80816
2-methyl-N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinoline
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CO)CCC2CC=CC=C2N1
Reaction #80817
2-hydroxymethyl-2-methyltetrahydroquinoline
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(CCc1ccc(Cl)cc1)(Cc1ccc(Cl)cc1)C(=O)OC(C)(C)C
Reaction #81147
tert-butyl 2-(4-chlorobenzyl)-2-{2-(4-chlorophenyl)ethyl}-3-oxobutanoate
Rendement 321.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC1c1ccc(O)c(F)c1
Reaction #91167
title compound
Rendement 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1ccc(C2CC2C(=O)O)cc1F
Reaction #91239
title compound
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC1c1ccc(OCc2cccc(SC3CCCC3)n2)c(F)c1
Reaction #91240
title compound
Rendement 92.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC1c1ccc(OCc2cccc(SC3CCC3)n2)c(F)c1
Reaction #91241
title compound
Rendement 92.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC1c1ccc(OCc2cccnc2SC2CCCC2)c(F)c1
Reaction #91242
title compound
Rendement 101.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC1c1ccc(OCc2cccnc2SC2CCC2)c(F)c1
Reaction #91243
title compound
Rendement 102.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(C(=O)SCC2C(=O)OCC2c2ccccc2)cc1
Reaction #93538
title compound
Rendement 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccccc1)c1ccccc1F
Reaction #93540
title compound
Rendement 67.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCC(c2ccccc2)C1CS
Reaction #93541
title compound
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1ccccc1-c1ccccc1)C(=O)OCC
Reaction #96089
diethyl (2-phenylbenzyl)malonate
Rendement 97.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cc1ccccc1-c1ccccc1)C(=O)O
Reaction #96090
(2-phenylbenzyl)malonic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(NC(=O)c2ccoc2)CCCCC1
Reaction #161001
title compound
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1(C(=O)O)CCCCC1)c1ccoc1
Reaction #161002
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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