An alternative total synthesis of Aigialomycin D
Synthetic Communications(2024)
摘要
Aigialomycin D, a 14-membered benzannulated macrolactone, was synthesized in a simple, efficient and stereoselective approach using inexpensive and commonly accessible starting materials. The main steps in this convergent synthesis are Corey-Fuchs reaction, Yamaguchi esterification and ring closing metathesis (RCM).
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关键词
Resorcylic acid lactones,aigialomycins,Corey-Fuchs reaction,Wittig olefination,Yamaguchi macrolactonization
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