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Stereoselective synthesis of (+)-hyptolide
Authors:Juan MurgaJorge Garc?&  #x  a-Fortanet,Miguel Carda
Affiliation:a Depart. de Q. Inorgánica y Orgánica, Univ. Jaume I, Castellón, E-12080 Castellón, Spain
b Depart. de Q. Orgánica, Univ. de Valencia, E-46100 Burjassot, Valencia, Spain
Abstract:The first total synthesis of the naturally occurring lactone (+)-hyptolide is described. Ethyl l-lactate was the chiral starting material. Key steps of this 15-step synthesis were a Brown's asymmetric allylation, a Carreira's asymmetric ethynylation and a ring closing metathesis.
Keywords:(+)-hyptolide   ring-closing metathesis   asymmetric allylboration   asymmetric ethynylation   chiral pool
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