4-methylphenylboronic acid

Cc1ccc(-c2ccccc2[N+](=O)[O-])cc1
Reaction #2005
product
Rendimiento 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1cc(OCc2ccc(B(O)O)cc2)c2ccccc2n1.Cl
Reaction #5768
4-[(2-ethylquinolin-4-yloxy)methyl]phenylboronic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OB(O)c1ccc(CBr)cc1
Reaction #5769
4-bromomethylphenylboronic acid
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccc(-c2cc(-c3ccc(O)c(F)c3)nc3ccc(O)cc23)cc1
Reaction #7342
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-methylphenyl)quinolin-6-ol
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(N2CCc3ncnc(Nc4ccc(C(F)(F)F)cc4)c3C2)cc1
Reaction #47918
desired compound
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-n2c(C(=O)N3CCC(F)(F)CC3)cc3cc(OC4CCN(C(C)C)CC4)ccc32)cc1
Reaction #48137
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-n2c(C(=O)N3CCOCC3)cc3cc(OC4CCN(C(C)C)CC4)ccc32)cc1
Reaction #48147
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSc1ccc(C2=C(c3ccc(C)cc3)CCC2)cc1
Reaction #65802
1-[2-(4-methylphenyl)cyclopenten-1-yl]-4-(methylthio)benzene
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1ccc(-c2ccccc2-c2nnnn2-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #65893
5-(4'-methylbiphenyl-2-yl)-1-(4-nitrophenyl)-1H-tetrazole
Rendimiento 95.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
OB(O)c1ccc(CBr)cc1
Reaction #65896
4-bromomethylphenylboronic acid
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCc1cc(OCc2ccc(B(O)O)cc2)c2ccccc2n1.Cl
Reaction #65898
4-[(2-ethylquinolin-4-yloxy)methyl]phenylboronic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1ccc(-c2ccc(N3CCCN(c4ccc(-c5ccc(C)cc5)cn4)CC3)nc2)cc1
Reaction #77568
title compound
Rendimiento 42.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)c1ccc(B(O)O)cc1
Reaction #77699
4-Carboxyphenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(-c2c(C(C)N=[N+]=[N-])nc3scc(C)n3c2=O)cc1
Reaction #86562
desired product
Rendimiento 61.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CSc1nn(-c2ccc(C)cc2)c2cc(C3=CCNCC3)ccc12
Reaction #155935
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-c2cc(C)c(C=O)s2)cc1
Reaction #156609
3-Methyl-5-p-tolylthiophene-2-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-c2ccccc2S(=O)(=O)/N=C/N(C)C)cc1
Reaction #158838
title compound
Rendimiento 82.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-c2nc(N3CCS(=O)(=O)CC3)nc3c2CCNCC3)cc1
Reaction #159988
title compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-n2cc([N+](=O)[O-])cn2)cc1
Reaction #162759
title compound
Rendimiento 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(-c2ccc(C#C[Si](C)(C)C(C)(C)C)nc2)cc1
Reaction #163321
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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