Approaches towards the total synthesis of carolacton: synthesis of C1–C16 fragment
Tetrahedron Letters(2015)
摘要
A stereoselective synthesis of the C1–C16 segment of biofilm inhibitor carolacton has been achieved. The synthetic strategy involves Sharpless asymmetric epoxidation, Roush crotylation, Steglich esterification, RCM reaction and selective reduction of a disubstituted olefin in the presence of a trisubstituted olefin using in situ generated diimide.
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关键词
Carolacton,Steglich esterification,Ring closing metathesis,Roush crotylation,Diimide reduction
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