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Published on: August 1, 2018
A synthesis of the chlorosulfolipid mytilipin A via a longest linear sequence of seven steps
Won-Jin Chung1, Joseph S Carlson, D Karl Bedke
1Department of Chemistry, University of California, Irvine, 1102 Natural Sciences II, Irvine, CA 92697-2025 (USA) http://www.chem.uci.edu/∼cdv.
Abstract:
Magnificent seven: The chlorosulfolipid mytilipin A was synthesized in racemic form in seven steps and in enantioenriched form in eight steps. Key transformations include a highly diastereoselective bromoallylation of a sensitive α,β-dichloroaldehyde, a kinetic resolution of a vinyl epoxide, a convergent and highly Z-selective alkene cross-metathesis, and a chemoselective and diastereoselective dichlorination of a complex diene.
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