Stereoselective Syntheses of Rolliniastatin 1, Rollimembrin, and Membranacin
Journal of the American Chemical Society2005Vol. 127(29), pp. 10396–10399
Citations Over TimeTop 10% of 2005 papers
Abstract
A radical cyclization of beta-alkoxyvinyl sulfoxides-Pummerer rearrangement-allylation protocol was successfully applied to the synthesis of the threo/cis/threo/cis/erythro bis-oxolane moiety in rolliniastatin 1 (1), rollimembrin (2), and membranacin (3).
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