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Toward the synthesis of cobyric acid. Enantioselective syntheses of completely differentiated ring D synthons
Authors:Wang Hui  Tassa Carlos  Jacobi Peter A
Affiliation:Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, USA.
Abstract:Alkyne acids 11 were prepared in an enantioselective fashion from allylic ester derivatives 18 or 20 by Ireland-Claisen rearrangement, followed by Si-assisted elimination of HBr. The title compounds are attractive ring D synthons for an ongoing synthesis of cobyric acid.
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