Synthesis of the enantiomers of umbelactone. Configurational assignment of the natural product

Rosa M. Ortuño, Joaquim Bigorra, Josep Font

Research output: Contribution to journalArticleResearchpeer-review

38 Citations (Scopus)

Abstract

Both (+)- and (-)-umbelactone have been synthetized from (R)-γ-hydroxymethyl-γ-butyrolactone and D-ribonolactone, respectively. The absolute configuration of the natural product has shown to beR-(+). © 1987.
Original languageEnglish
Pages (from-to)2199-2202
JournalTetrahedron
Volume43
Issue number9
DOIs
Publication statusPublished - 1 Jan 1987

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