Enantioselective Syntheses of Wickerols A and B
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DOI: 10.1021/jacs.3c00448
Abstract: The evolution of a successful strategy for the synthesis of the strained, cage-like antiviral diterpenoids wickerols A and B is described. Initial attempts to access the carbocyclic core were surprisingly challenging and in retrospect, presaged… read more here.
Keywords: stereochemistry; enantioselective syntheses; syntheses wickerols;