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Boron-stabilized acylation

Acylation of (2) with benzonitrile gives an intermediate which yields acetophenone (52%) on hydrolysis with 3 M HCl. This seems to be the only recorded reaction of a boron-stabilized carbanion with a nitrile. ... [Pg.498]

C(l)-Phenyl-substituted alkenyloxyboranes (13) may be prepared by the acylation of boron-stabilized carbanions with methyl benzoate (Scheme 12). ... [Pg.244]

See other pages where Boron-stabilized acylation is mentioned: [Pg.94]   
See also in sourсe #XX -- [ Pg.497 ]

See also in sourсe #XX -- [ Pg.497 ]



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Acylation boron-stabilized carbanions

Benzoic acid acylation of boron-stabilized carbanions

Boranes, alkenyloxyreactions with ketones via acylation of boron-stabilized carbanions

Boron-stabilized

Boronates stability

Ketones, a-phenylthio via acylation of boron-stabilized carbanions

Ketones, phenyl via acylation of boron-stabilized carbanions

Ketones, y-hydroxy via acylation of boron-stabilized carbanions

Y-Keto acids via acylation of boron-stabilized carbanions

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