#1235922

CCOC(=O)C(=C1CCCCCN1C)c1ccc(Cl)cc1
Reaction #55701
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(=O)C(=C1CCCN1C(C)C)c1ccc(Cl)cc1
Reaction #190661
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=C(C(=O)OCC)c1ccc(Cl)cc1
Reaction #246050
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(CC1CCCC1)c1ccc(Cl)cc1
Reaction #261985
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=c1c(-c2ccc(Cl)cc2)c[nH]n1-c1ncccn1
Reaction #342676
1-pyrimid-2-yl-4-(4-chloro-phenyl)pyrazolin-5-one
Выход 26.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
CCOC(=O)C(=C1CCCN1C)c1ccc(Cl)cc1
Reaction #404079
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C(CC1CCCC1)c1ccc(Cl)cc1
Reaction #485601
2-(4-chloro-phenyl)-3-cyclopentyl-propionic acid ethyl ester
Выход 90.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCOC(=O)C(CC1CCCC1)c1ccc(Cl)cc1
Reaction #517294
2-(4-chloro-phenyl)-3-cyclopentyl-propionic acid ethyl ester
Выход 90.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCOC(=O)C(C=O)c1ccc(Cl)cc1
Reaction #727991
2-(4-chlorophenyl)-3-oxo-propanoic acid ethyl ester
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CCOC(=O)C(CC(C)C)c1ccc(Cl)cc1
Reaction #895153
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)/C(=C/N(C(=O)OC(C)(C)C)C(C)C)c1ccc(Cl)cc1
Reaction #1009350
(E)-ethyl 3-((tert-butoxycarbonyl)(isopropyl)amino)-2-(4-chlorophenyl)acrylate
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CCOC(=O)C(CC1CCCC1)c1ccc(Cl)cc1
Reaction #1053745
2-(4-chloro-phenyl)-3-cyclopentyl-propionic acid ethyl ester
Выход 90.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
O=c1c(-c2ccc(Cl)cc2)c[nH]n1-c1ncccn1
Reaction #1065119
1-pyrimid-2-yl-4-(4 -chlorophenyl)-pyrazolin-5-one
Выход 26.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
Cc1ccc(-c2c[nH]c3ccnc(NCCc4ccccc4)c3c2=O)cc1
Reaction #1131505
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cc1ccc(-c2c[nH]c3ccnc(NCCc4ccccc4)c3c2=O)cc1
Reaction #1131506
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cc1ccc(-c2c[nH]c3ccnc(NCCc4ccccc4)c3c2=O)cc1
Reaction #1131509
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CCOC(=O)C(C=O)c1ccc(Cl)cc1
Reaction #1153709
ethyl 2-(4′-chlorophenyl)-2-formylacetate
Выход 78.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_06
CCOC(=O)C(CCC(=O)OC(C)(C)C)c1ccc(Cl)cc1
Reaction #1279522
2-(4-chlorophenyl)-pentanedioic acid 5-tert-butyl ester 1-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
CCOC(=O)C(=C1CCCN1C)c1ccc(Cl)cc1
Reaction #1365212
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_07
CCOC(=O)C(=C1CCCN1C(C)C)c1ccc(Cl)cc1
Reaction #1365214
product
Выход 8.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_07
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