Stereoselection in iodolactonisations of 3-silyloxy-5-alkenoic acids

Simon B. Bedford, Garry Fenton, David W. Knight, Duncan Shaw

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

Iodolactonisations of (Z)- or (E)-3-silyloxy-5-alkenoic acids [1 and 7] both lead to transdisubstituted valerolactones [6 and 8], which differ only in the stereochemistry of the iodine substituent.
Original languageEnglish
Pages (from-to)6505-6506
Number of pages2
JournalTetrahedron Letters
Volume33
Issue number43
DOIs
Publication statusPublished - 1992

Keywords

  • methyl groups

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