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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
In Bloodagonistsantagonists & inhibitorschemical synthesis

Papers overview

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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… 
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… 
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. YeM. 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… 
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… 
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… 
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… 
Highly Cited
2008
Highly Cited
2008
Cross-coupling reactions of aryl pivalates with boronic acids.
The first cross-coupling of acylated phenol derivatives has been achieved. In the presence of an air-stable Ni(II) complex… 
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… 
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