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Formation of β,β-dihaloenones from halogenated tertiary alkynols

  • New York University

Research output: Contribution to journalArticlepeer-review

33 Citations (Scopus)

Abstract

Halogenated alkynols react with N-halosuccinimides and catalytic amounts of Koser's reagent to afford mixed β,β-dihaloenones, useful templates for aryl and alkyl substituted enones.

Original languageEnglish
Pages (from-to)2285-2288
Number of pages4
JournalTetrahedron Letters
Volume33
Issue number17
DOIs
Publication statusPublished - 17 Apr 1992
Externally publishedYes

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