Synthetic efforts towards the stereoselective synthesis of NF00659B(1)

NF00659B(1)立体选择性合成的合成研究

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Abstract

NF00659B(1) is a novel α-pyrone diterpenoid natural product with potent anti-colon cancer activity. A stereoselective approach to the 2,2-dimethyl oxepanol core of NF00659B(1) is described enlisting a sequence of olefinic ester ring-closing metathesis, epoxidation, and Grignard addition. This strategy paves the way to a total synthesis of NF00659B(1) for further biological studies.

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