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引用
期刊论文
Asymmetric Synthesis of Antimalarial Alkaloids (+)-Febrifugine and(+)-Isofebrifugine
Synlett 2003, No. 11, 1663-1667,-0001,():
Diastereoselective a-amidoalkylation of N,O-acetal, derivated from controlled regio and diastereoselective reduction of (S)-N-(4-methoxybenzyl)-3-silyloxyglutarimide provided two diastereomeric 6-allyl-5-silyloxy-2-piperidinones in 76:24 selectivity. The transformation of the major diastereomer into a known advanced intermediate allowed the synthesis of (+)-febrifugine and (+)-isofebrifugine.
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