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Title: Enantioselective Total Synthesis of (+)-Peniciketals A and B: Two Architecturally Complex Spiroketals. Author: Deng Y, Yang CH, Smith Iii AB. Journal: J Am Chem Soc; 2021 Feb 03; 143(4):1740-1744. PubMed ID: 33496178. Abstract: The enantioselective total syntheses of (+)-peniciketals A and B, two members of a family of architecturally complex spiroketals, have been achieved. Key synthetic transformations comprise Type I Anion Relay Chemistry (ARC) to construct the benzannulated [6,6]-spiroketal skeleton, a Negishi cross-coupling/olefin cross-metathesis reaction sequence to generate the trans-enone structure, and a late-stage large fragment union exploiting our recently developed photoisomerization/cyclization tactic.[Abstract] [Full Text] [Related] [New Search]