Total Synthesis of Sanctolide A and Formal Synthesis of (2)-Sanctolide A.

J Org Chem

Department of Chemistry, University of Kansas, 1251 Wescoe Hall Drive, Lawrence, Kansas 66045-7582, United States.

Published: January 2023

Two synthetic strategies employing phosphate tether-mediated one-pot sequential protocols for the total synthesis of the polyketide nonribosomal peptide macrolide, sanctolide A, and the formal synthesis of the (2)-epimer of sanctolide A are reported. In this work, a phosphate tether-mediated one-pot sequential ring-closing metathesis/cross metathesis/substrate-controlled "H"/tether removal approach was developed to accomplish the total synthesis of the natural product sanctolide A.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10718183PMC
http://dx.doi.org/10.1021/acs.joc.2c01922DOI Listing

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