Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction

Thomas R. Hoye, Paul R. Hanson, Linda E. Hasenwinkel, Elizabeth A. Ramirez, Zhiping Zhuang

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Each diastereomer of model butenolides 3 was synthesized from appropriate antipodes of two propylene oxide molecules. Concomitant translactonization reactions have important stereochemical ramifications.

Original languageEnglish (US)
Pages (from-to)8525-8528
Number of pages4
JournalTetrahedron Letters
Volume35
Issue number46
DOIs
StatePublished - Nov 14 1994

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