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Lithium hexamethyldisilazide, reaction with ketones

The products of the reaction of ketones with lithium hexamethyldisilazide have been studied by Collum and co-workers by an extensive use of the Li and NMR spectroscopy Vun couplings have been found to be particularly useful. [Pg.168]

This reaction can sometimes be useful in synthesis. In the Honda et al. formal synthesis of securinine,2h N-benzylamino-ketone (97) was treated with lithium hexamethyldisilazide and then sorbic anhydride. This gave dienyl ester 98 by O-alkylation of the initially formed enolate anion. When the nitrogen protecting group was... [Pg.736]


See other pages where Lithium hexamethyldisilazide, reaction with ketones is mentioned: [Pg.878]    [Pg.1348]    [Pg.84]    [Pg.404]    [Pg.627]    [Pg.1366]    [Pg.373]    [Pg.147]    [Pg.147]    [Pg.414]    [Pg.231]    [Pg.314]    [Pg.251]    [Pg.434]    [Pg.378]    [Pg.47]   
See also in sourсe #XX -- [ Pg.736 ]




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Hexamethyldisilazide

Hexamethyldisilazides

Ketone reaction with lithium

Ketones lithium hexamethyldisilazide

Ketones, reaction with hexamethyldisilazide

Lithium hexamethyldisilazides

Lithium ketones

Reaction with ketone

Reaction with lithium

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