A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones

Michael T. Crimmins, Caroline J. Diaz, Kyle A. Emmitte

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.

Original languageEnglish
Pages (from-to)179-183
Number of pages5
JournalHeterocycles
Volume62
StatePublished - 1 Jan 2004

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