methyl acetate

COC(=O)c1ccccc1NC(=O)CCc1ccccc1
Reaction #257536
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(C)=O
Reaction #286473
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc2nn(C)cc2c1C1CC1CNC(C)=O
Reaction #296554
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C[C@@H](COc1cccc(CC(=O)O)c1)CN(Cc1cccc(C(F)(F)F)c1F)CC(c1ccccc1)c1ccccc1.Cl
Reaction #316280
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C[C@@H](COc1cccc(CC(=O)O)c1)CN(Cc1ccc(F)c(C(F)(F)F)c1)CC(c1ccccc1)c1ccccc1.Cl
Reaction #316281
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cccc(CN(CC(c2ccccc2)c2ccccc2)C[C@@H](C)COc2cccc(CC(=O)O)c2)n1.Cl
Reaction #316282
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1ccc(CN(CC(c2ccccc2)c2ccccc2)C[C@@H](C)COc2cccc(CC(=O)O)c2)cc1.Cl
Reaction #316283
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1ccc(CN(CC(c2ccccc2)c2ccccc2)C[C@@H](C)COc2cccc(CC(=O)O)c2)c(F)c1.Cl
Reaction #316284
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1ccc(CN(CC[C@@H](C)Oc2cccc(CC(=O)O)c2)CC(c2ccccc2)c2ccccc2)c(OC)c1.Cl
Reaction #316286
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1ccc(CN(CC[C@@H](C)Oc2cccc(CC(=O)O)c2)CC(c2ccccc2)c2ccccc2)cc1.Cl
Reaction #316287
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C[C@H](CCN(Cc1ccccc1OCF)CC(c1ccccc1)c1ccccc1)Oc1cccc(CC(=O)O)c1.Cl
Reaction #316288
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C[C@H](CCN(Cc1cccc(C(F)(F)F)c1)CC(c1ccccc1)c1ccccc1)Oc1cccc(CC(=O)O)c1.Cl
Reaction #316289
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C[C@H](CCN(Cc1cccc(C(F)(F)F)c1F)CC(c1ccccc1)c1ccccc1)Oc1cccc(CC(=O)O)c1.Cl
Reaction #316290
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C[C@H](CCN(Cc1ccc(F)c(C(F)(F)F)c1)CC(c1ccccc1)c1ccccc1)Oc1cccc(CC(=O)O)c1.Cl
Reaction #316291
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1ccc(CN(CC[C@@H](C)Oc2cccc(CC(=O)O)c2)CC(c2ccccc2)c2ccccc2)cc1F.Cl
Reaction #316292
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1nc(-c2cccc(N)c2)no1
Reaction #318027
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)c1ccc(SC)cc1N
Reaction #318921
methyl 2-amino-4-(methylthio)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCS(=O)(=O)c1cnc(Oc2c(C)c(CC(=O)OC)cc3ccc(F)cc23)c(Br)c1
Reaction #325831
[4-(3-bromo-5-ethanesulfonyl-pyridin-2-yloxy)-6-fluoro-3-methyl-naphthalen-2-yl]-acetic acid methyl ester
収率 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
—
Reaction #325917
tan oil
収率 84.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC1=CC(=O)C=C2CC[C@@H]3[C@H](CC[C@]4(C)C(=O)CC[C@@H]34)[C@@]12C
Reaction #347074
crude product
収率 183.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
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