C/Se bond cleavage of functionalized selenides by lithium arenides: Application to the geminal di-allylation of the carbonyl group of aldehydes and ketones

A. Krief, A. Nazih

Résultats de recherche: Contribution à un journal/une revueArticleRevue par des pairs

Résumé

Selenoacetals as well as mixed (O,Se) acetals react with lithium arenides and produce, besides lithium selenolates, α-selenoalkyllithiums or α-alkoxyalkyllithiums respectively. We took advantage of these reactions as well as of the ones involving the synthesis of alkyllithiums from selenides to propose an original method for geminal di-allylation of the carbonyl group of aldehydes and ketones.
langue originaleAnglais
Pages (de - à)8115-8118
Nombre de pages4
journalTetrahedron Letters
Volume36
Numéro de publication44
Etat de la publicationPublié - 1 janv. 1995

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