Doubly diastereoselective iodolactonizations: Olefin and face selectivity in nona-2,7-diene-5-carboxylic acid cyclizations

John C. McKew, Marilyn M. Olmstead, Mark J. Kurth

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

Nonracemic nonadienoic acids (v) were subjected to iodolactonization conditions and, by doubly diastereoselective cyclization, delivered enantiomerically pure iodo lactones replete with up to five contiguous stereogenic centers.

Original languageEnglish (US)
Pages (from-to)3389-3393
Number of pages5
JournalJournal of Organic Chemistry
Volume59
Issue number12
StatePublished - 1994

ASJC Scopus subject areas

  • Organic Chemistry

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