A simple and efficient stereoselective total synthesis of (−)-sedridine

Saroja Nuguri , Laxminarayana Eppakayala , Naresh Kumar Vuppula , Prasad Kottapalli Rajasekhara
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引用次数: 3

Abstract

An asymmetric synthesis of the piperidine alkaloid (−)-sedridine isolated from Sedum acre, has been accomplished starting from S-malic acid as the chiral precursor employing Maruoka Keck allylation, azide nucleophillic substitution and ring closing metathesis as the key steps.

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一种简单、高效的立体选择性全合成(−)-赛定胺
以s -苹果酸为手性前体,经Maruoka Keck烯丙化、叠氮化物亲核取代和合环复分解为关键步骤,完成了从景天属植物中分离得到的胡椒碱(−)-景天碱的不对称合成。
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