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Tetrahedron: Asymmetry

The first synthesis of a 12-membered macrolide natural product via a RCM protocol: determination of absolute stereochemistry

PR Krishna, R Srinivas

文献索引:Krishna, Palakodety Radha; Srinivas, Ravula Tetrahedron Asymmetry, 2008 , vol. 19, # 9 p. 1153 - 1160

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被引用次数: 9

摘要

The first synthesis of (10S, 12R)-10-hydroxy-12-methyl-1-oxacyclododecane-2, 5-dione and its C12 epimer is reported, thereby assigning the absolute stereochemistry of the natural product. The strategy utilizes a syn selective reduction, Yamaguchi esterification, and ring- closing metathesis as the key steps.