The Catalytic Enantioselective Total Synthesis of (+)-Liphagal

Joshua J. Day, Ryan M. McFadden, Scott C. Virgil, Helene Kolding, Jennifer L. Alleva, Brian M. Stoltz

Research output: Contribution to journalArticlepeer-review

59 Scopus citations

Abstract

Ring a ding: The meroterpenoid natural product (+)-liphagal has been synthesized enantioselectively in 19 steps from commercially available materials. The trans-homodecalin system was achieved by ring expansion followed by stereoselective hydrogenation. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Original languageEnglish (US)
Pages (from-to)6814-6818
Number of pages5
JournalAngewandte Chemie International Edition
Volume50
Issue number30
DOIs
StatePublished - Jun 10 2011
Externally publishedYes

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