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Ring expansion of an α-bromoalkynol camphor by means of iodine and Koser's reagent

  • New York University

Research output: Contribution to journalArticlepeer-review

30 Citations (Scopus)

Abstract

The bromoethynyl adduct of camphor was treated with equimolar amounts of iodine and Koser's reagent (HTIB) to afford in good yield and in good stereospecificity a (Z)-bromoiodoenone, a synthon for enantiospecific syntheses.

Original languageEnglish
Pages (from-to)4277-4280
Number of pages4
JournalTetrahedron Letters
Volume34
Issue number27
DOIs
Publication statusPublished - 2 Jul 1993
Externally publishedYes

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