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  2. Boronic acid - Wikipedia

    en.wikipedia.org/wiki/Boronic_acid

    Protodeboronation is a chemical reaction involving the protonolysis of a boronic acid (or other organoborane compound) in which a carbon-boron bond is broken and replaced with a carbon-hydrogen bond. Protodeboronation is a well-known undesired side reaction , and frequently associated with metal-catalysed coupling reactions that utilise boronic ...

  3. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  4. CBS catalyst - Wikipedia

    en.wikipedia.org/wiki/CBS_catalyst

    The general outline for the organic synthesis of a CBS catalyst is shown below. The first leg of the reaction sequence starts from the azeotropic dehydration of a boronic acid (1) such as one based on toluene to a boroxine (2). This boroxine reacts with the proline derivative (3d) to form the basic oxazaborolidine CBS catalyst (4).

  5. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  6. Kharasch–Sosnovsky reaction - Wikipedia

    en.wikipedia.org/wiki/Kharasch–Sosnovsky_reaction

    The Kharasch–Sosnovsky reaction is a method that involves using a copper or cobalt salt as a catalyst to oxidize olefins at the allylic position, subsequently condensing a peroxy ester (e.g. tert-Butyl peroxybenzoate) or a peroxide resulting in the formation of allylic benzoates or alcohols via radical oxidation. [1]

  7. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    Structure of a rare monomeric boron hydride, R = i-Pr. [4] The most-studied class of organoboron compounds has the formula BR n H 3−n. These compounds are catalysts, reagents, and synthetic intermediates. The trialkyl and triaryl derivatives feature a trigonal-planar boron center that is typically only weakly Lewis acidic.

  8. Michaelis–Arbuzov reaction - Wikipedia

    en.wikipedia.org/wiki/Michaelis–Arbuzov_reaction

    [2] [3] This reaction is widely used for the synthesis of various phosphonates, phosphinates, and phosphine oxides. Several reviews have been published. [4] [5] The reaction also occurs for coordinated phosphite ligands, as illustrated by the demethylation of {(C 5 H 5)Co[(CH 3 O) 3 P] 3} 2+ to give {(C 5 H 5)Co[(CH 3 O) 2 PO] 3} −, which is ...

  9. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    [4] [5] The reaction has since been extended to the synthesis of β-keto esters from the condensation between aldehydes and diazo esters. [6] The general reaction scheme is as follows: General Scheme for Buchner Reaction. The reaction yields two possible carbonyl compounds (I and II) along with an epoxide (III). The ratio of the products is ...