dicyclohexylmethanamine

COC(=O)/C(C)=C/c1ccc(N(C)C)cc1
Reaction #42155
(E)-3-(4-dimethylaminophenyl)-2-methylacrylic acid methyl ester
المردود 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1ccc(/C=C/c2ccccc2)cc1
Reaction #42156
(trans)-4-acetylstilbene
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)/C(C)=C/c1c(C)cccc1C
Reaction #42157
(E)-3-(2,6-dimethylphenyl)-2-methylacrylic acid methyl ester
المردود 75.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)/C(C)=C/c1ccc(N(C)C)cc1
Reaction #42174
(E)-3-(4-dimethylaminophenyl)-2-methylacrylic acid methyl ester
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1ccc(/C=C/c2ccccc2)cc1
Reaction #42175
(trans)-4-acetylstilbene
المردود 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)/C(C)=C/c1c(C)cccc1C
Reaction #42176
(E)-3-(2,6-dimethylphenyl)-2-methylacrylic acid methyl ester
المردود 75.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C=Cc1c(C(C)=O)cc(OCc2ccccc2)cc1[N+](=O)[O-]
Reaction #61657
methyl 3-(2-acetyl-4-benzyloxy-6-nitro-phenyl)-acrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc2cc([C@H](C)C(=O)O)ccc2c1
Reaction #63658
naproxen
المردود 208.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C[Si](C)(C)CCOCn1cc2cc(C=O)ccc2n1
Reaction #156375
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cc1ccccc1/C=C/C(=O)OC(C)(C)C
Reaction #172137
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#CC=Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #184421
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(C=Cc2ccccc2)cc1
Reaction #189686
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(C=CCl)c(C(F)(F)F)nn1C
Reaction #250428
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C(C)=Cc1ccc(N(C)C)cc1
Reaction #251268
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
—
Reaction #362397
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
Cc1c(C=CCl)c(C(F)(F)F)nn1C
Reaction #380527
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)C(C)=Cc1ccc(N(C)C)cc1
Reaction #384628
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)C(C)=Cc1c(C)cccc1C
Reaction #385180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc2nn(COCC[Si](C)(C)C)cc2cc1Br
Reaction #425639
title compound
المردود 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCCCOC(=O)/C=C/c1ccc(OC)nc1NC(=O)C(C)(C)C
Reaction #507849
product
المردود 95.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
الصفحة 1التالي