Enantioselective synthesis of decarestrictine J
01 natural sciences
0104 chemical sciences
DOI:
10.1016/j.tetlet.2009.10.035
Publication Date:
2009-10-14T18:47:29Z
AUTHORS (3)
ABSTRACT
An efficient total synthesis of decarestrictine J has been achieved using ring-closing metathesis and Yamaguchi esterification as key steps. The stereogenic centres were generated by means of iterative hydrolytic kinetic resolution (HKR) of racemic epoxides.
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