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Diboryl compounds do not yield aldehydes with alkaline hydrogen peroxide. Instead there is r d hydrolysis, presumably via a boron-stabilized carbanion (see Volume 1, Ch ter 2.6) which is protonated and then oxidized to the alcohol (equation 16). ... [Pg.596]

Diboryl compounds yield alkenes on reaction with chromic acid (equation 45), a reaction also noted in a peracid oxidation and oxidation with pyridinium chlorochromate. ... [Pg.601]

See other pages where 1,1 -Diboryl compounds oxidation is mentioned: [Pg.602] [Pg.602]