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Total synthesis of pleurolactone
Authors:Toyoharu Kobayashi  Masako Ishida  Kazuhiro Imaida  Hideki Abe  Hisanaka Ito
Affiliation:School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan
Abstract:The stereoselective total synthesis of pleurolactone has been accomplished in 7 steps. The key synthetic features were the construction of four contiguous stereocenters using an endo-selective Diels-Alder reaction and high diastereoselective dihydroxylation.
Keywords:Terpenoids  Pleurolactone  Diels-Alder reaction  Diastereoselective dihydroxylation  Hexahydrobenzofuran
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