Concise and efficient synthesis of eliglustat
SYNTHETIC COMMUNICATIONS(2018)
摘要
Eliglustat, a ceramide glucosyltransferase inhibitor, was synthesized in six steps with 28.4% overall yield. The key features include the use of a diastereoselective aldol reaction to construct two contiguous stereocenters and a selective sulfonylation of a 1,3-diol catalyzed by dibutyltin oxide. [GRAPHICS] .
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关键词
Aldol reaction,eliglustat,selective sulfonylation,stereogenic centers
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