Synthesis of the Originally Proposed Structure of Palmerolide C
作者:Gordon J. Florence、Joanna Wlochal
DOI:10.1002/chem.201203067
日期:2012.11.5
A stereoselective synthesis of the proposed structure of palmerolide C (1), a cytotoxic marinemacrolide isolated from the Antarctic tunicate Synoicum adareanum, utilizes a convergent carbonyl‐based couplingstrategy to construct the C1–C24 carbon skeleton (see scheme). Compound 1 was shown to be a diastereomer of palmerolide C, and the structural revision of the natural product is proposed.