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Facile Diastereoselective Ester Enolate Claisen Rearrangements of Allyl Fluoroacetates

  • SUNY Albany

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

The diastereoselective ester enolate Claisen rearrangement of allyl fluoroacetate esters results from stereoselective deprotonation of the ester to form the E enolate.

Original languageEnglish
Pages (from-to)3663-3665
Number of pages3
JournalJournal of Organic Chemistry
Volume50
Issue number19
DOIs
StatePublished - Sep 1985

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