4-(methoxycarbonyl)phenylboronic acid

COC(=O)c1ccc(Oc2ccc(NC(C)=O)cc2)cc1
Reaction #51652
methyl 4-(4-acetamidophenoxy)benzoate
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCN(CCC)C(=O)C1=Cc2ccc(-c3ccc(C(=O)OC)cc3)cc2N=C(N)C1
Reaction #66304
methyl 4-((1E,4E)-2-amino-4-(dipropylcarbamoyl)-3H-benzo[b]azepin-8-yl)benzoate
Выход 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccc(-c2cc(C(=O)N3CCC4(CC3)CC(=O)c3cc(-c5cnn(C)c5)ccc3O4)nc3c(C4CC4)cccc23)cc1
Reaction #66742
Methyl 4-(8-cyclopropyl-2-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4′-piperidin]-1′-yl]carbonyl}quinolin-4-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccc(-n2nc(C)c3ccc(C(=O)N4CCC5(CC4)CC(=O)c4cc(-c6cnn(C)c6)ccc4O5)cc32)cc1
Reaction #66743
Methyl 4-(3-methyl-6-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4′-piperidin]-1′-yl]carbonyl}-1H-indazol-1-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cccc(-c2cc(C(=O)N3CCC4(CC3)CC(=O)c3cc(-c5cnn(C)c5)ccc3O4)cc3c2ccn3C2CC2)c1
Reaction #66745
Methyl 3-(1-cyclopropyl-6-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4′-piperidin]-1′-yl]carbonyl}-1H-indol-4-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccccc1-c1cc(C(=O)N2CCC3(CC2)CC(=O)c2cc(-c4cnn(C)c4)ccc2O3)cc2c1ccn2C1CC1
Reaction #66746
Methyl 2-(1-cyclopropyl-6-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4′-piperidin]-1′-yl]carbonyl}-1H-indol-4-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cccc(-n2nc(C)c3cc(C(=O)N4CCC5(CC4)CC(=O)c4cc(-c6cnn(C)c6)ccc4O5)ccc32)c1
Reaction #66748
Methyl 3-(3-methyl-5-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4′-piperidin]-1′yl]carbonyl}-1H-indazol-1-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOc1cc(C(=O)OC(C)(C)C)cc(OCC)c1-c1ccc(C(=O)OC)cc1
Reaction #66760
4-tert-Butyl 4′-methyl 2,6-diethoxybiphenyl-4,4′-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccc(-c2ccc3c(c2)CC[C@H](CNC[C@H](O)COc2ccccc2)O3)cc1.CS(=O)(=O)O
Reaction #75973
product
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)c1ccc(-c2nc3ccc(OC)cc3cc2C)cc1
Reaction #84056
methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate
Выход 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccc(-c2ccc3cc(O)ccc3n2)cc1
Reaction #84060
4-(6-hydroxyquinolin-2-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(-c2ccc3cc(O)ccc3n2)cc1
Reaction #84086
methyl 4-(6-hydroxyquinolin-2-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)cc1
Reaction #84096
product
Выход 40.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)cc1
Reaction #84097
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(-c2cc(N)c3cc(OC)ccc3n2)cc1
Reaction #84103
product
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(-c2cnc(Nc3ccc4c(c3)OCCO4)nc2Nc2ccc3c(c2)OCCO3)cc1
Reaction #158830
N2,N4-bis(3,4-ethylenedioxyphenyl)-5-(4-methoxycarbonylphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(-c2cnc(Nc3ccc4c(c3)OCCO4)nc2Nc2ccc3c(c2)OCCO3)cc1
Reaction #163941
N2,N4-bis(3,4-ethylenedioxyphenyl)-5-(4-methoxycarbonylphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(-c2ccc(CN(C(=O)CN(C)S(=O)(=O)c3ccc(C)cc3)c3ccc(C(=O)OCc4ccccc4)c(OCc4ccccc4)c3)cc2)cc1
Reaction #169052
31
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(-c2ccc(CN(C(=O)CN(C)S(=O)(=O)c3ccc(C)cc3)c3ccc(C(=O)OCc4ccccc4)c(OCc4ccccc4)c3)cc2-c2ccccc2)cc1
Reaction #169058
39
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172731
title compound
Выход 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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