(3-methoxy-4-methoxycarbonylphenyl)boronic acid

CCn1cc(C(O)(C(C)c2ccc(-c3ccc(C(=O)OC)c(OC)c3)cc2Cl)C(F)(F)F)ccc1=O
Reaction #238732
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(-c2cnc(N)c(-c3cn(C(C)C)nn3)c2)ccc1C(=O)O
Reaction #719656
title compound
المردود 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc4c(c3)N(C)C(=O)CO4)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #1019574
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc(=O)n(C)c3)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #1029958
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COc1cc(-c2cnc(N)c(-c3cn(C(C)C)nn3)c2)ccc1C(=O)O
Reaction #1140299
title compound
المردود 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc(=O)n(C)c3)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #1183171
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CCn1cc(C(O)(C(C)c2ccc(-c3ccc(C(=O)OC)c(OC)c3)cc2Cl)C(F)(F)F)ccc1=O
Reaction #1183187
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COC(=O)c1ccc(-c2ccc([C@@H](Oc3cc(N4CCC5(CC4)C[C@@H](C(=O)O)N(C(=O)OCc4ccccc4)C5)nc(N)n3)C(F)(F)F)c(-n3ccc(C)n3)c2)cc1OC
Reaction #1586327
(S)-8-(2-amino-6-((R)-2,2,2-trifluoro-1-(3′-methoxy-4′-(methoxycarbonyl)-3-(3-methyl-1H-pyrazol-1-yl)-[1,1′-biphenyl]-4-yl)ethoxy)pyrimidin-4-yl)-2-((benzyloxy)carbonyl)-2,8-diazaspiro[4.5]decane-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
CCc1nccc(-c2ccc(C(=O)OC)c(OC)c2)c1C#Cc1ccc(N)nc1
Reaction #1616402
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc4c(c3)N(C)C(=O)CO4)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #2183924
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc4oc(=O)n(C)c4c3)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #2184011
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc4oc(=O)n(C)c4c3)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #2406785
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc4c(c3)N(C)C(=O)CO4)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #2473905
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09
COC(=O)c1ccc(-c2ccc(C(C)C(O)(c3ccc4oc(=O)n(C)c4c3)C(F)(F)F)c(Cl)c2)cc1OC
Reaction #2474000
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09
COC(=O)c1ccc(-c2cnc3sc(-c4cnc(N)c(C(F)(F)F)c4)nn23)cc1OC
Reaction #2496780
desired product
المردود 0.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08