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PROTODEBORONATION

Protodeboronation

Chemical reaction

Protodeboronation, or protodeborylation is a chemical reaction involving the protonolysis of a boronic acid (or other organoborane compound) in which

Protodeboronation

Tris(benzyltriazolylmethyl)amine

Chemical compound

reaction to proceed. TBTA is an effective CuAAC ligand for preventing protodeboronation when the alkyne or azide contains a boronic acid or boronic ester

Tris(benzyltriazolylmethyl)amine

Boronic acid

Organic compound of the form R–B(OH)2

meta-bromination of m-xylene which by standard AES would give the ortho product: Protodeboronation is a chemical reaction involving the protonolysis of a boronic acid

Boronic acid

Boronic_acid

Suzuki reaction

Cross-coupling reaction between boronic acid & an organohalide

organoboranes that are frequently used because they are less prone to protodeboronation compared to aryl boronic acids. They are easy to synthesize and can

Suzuki reaction

Suzuki_reaction

Bamford–Stevens reaction

Synthesis of alkenes by base-catalysed decomposition of tosylhydrazones

the benzylboronic acid via a zwitterionic intermediate, followed by protodeboronation of the benzylboronic acid under basic conditions, which results in

Bamford–Stevens reaction