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Boronic Acids

Known as: Acids, Boronic, Boronic Acids [Chemical/Ingredient] 
Inorganic or organic compounds that contain the basic structure RB(OH)2.
National Institutes of Health

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1,4-phenylenebis(boronic acid)1-aminocyclopropaneboronic acid2,3-difluorophenylboronic acid2-bromopyridine-5-boronic acid
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Aerobic copper-catalyzed organic reactions.
The chemistry of copper is extremely rich because it can easily access Cu0, CuI, CuII, and CuIII oxidation states allowing it to… 
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Review
2013
Review
2013
Exploiting the reversible covalent bonding of boronic acids: recognition, sensing, and assembly.
Boronic acids can interact with Lewis bases to generate boronate anions, and they can also bind with diol units to form cyclic… 
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Highly Cited
2012
Highly Cited
2012
Merging visible-light photocatalysis and transition-metal catalysis in the copper-catalyzed trifluoromethylation of boronic acids with CF3I.
  • Y. Ye, M. Sanford
  • Journal of the American Chemical Society
  • 2012
  • Corpus ID: 207080829
This communication describes the development of a mild method for the cross-coupling of arylboronic acids with CF(3)I via the… 
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Highly Cited
2011
Highly Cited
2011
Practical C-H functionalization of quinones with boronic acids.
A direct functionalization of a variety of quinones with several boronic acids has been developed. This scalable reaction… 
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Highly Cited
2010
Highly Cited
2010
Copper-mediated oxidative trifluoromethylation of boronic acids.
A copper-mediated oxidative cross-coupling of aryl- and alkenylboronic acids with (trifluoromethyl)trimethylsilane (Me(3)SiCF(3… 
Highly Cited
2010
Highly Cited
2010
A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids.
Boronic acids which quickly deboronate under basic conditions, such as polyfluorophenylboronic acid and five-membered 2… 
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Highly Cited
2009
Highly Cited
2009
A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.
Many boronic acids, including 2-heterocyclic, vinyl, and cyclopropyl derivatives, are inherently unstable, which can limit their… 
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Highly Cited
2007
Highly Cited
2007
Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction.
Organotrifluoroborates represent an alternative to boronic acids, boronate esters, and organoboranes for use in Suzuki-Miyaura… 
Highly Cited
2007
Highly Cited
2007
Highly efficient monophosphine-based catalyst for the palladium-catalyzed suzuki-miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters.
A highly active and efficient catalyst system derived from a palladium precatalyst and monophosphine ligands 1 or 2 for the… 
Highly Cited
1998
Highly Cited
1998
Potent and selective inhibitors of the proteasome: dipeptidyl boronic acids.
Potent and selective dipeptidyl boronic acid proteasome inhibitors are described. As compared to peptidyl aldehyde compounds… 
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