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

Research output: Contribution to journalArticlepeer-review

Abstract

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.
Original languageEnglish
Pages (from-to)8115-8118
Number of pages4
JournalTetrahedron Letters
Volume36
Issue number44
Publication statusPublished - 1 Jan 1995

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