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5-Hexadecanolide的不对称合成
引用本文:孙彬,张朝欣,张贵民,李赢,李裕林,彭立增.5-Hexadecanolide的不对称合成[J].中国化学,2005,23(9):1228-1230.
作者姓名:孙彬  张朝欣  张贵民  李赢  李裕林  彭立增
作者单位:[1]National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, Gansu 730000, China [2]Lu'nan Pharmaceutical Co., Ltd., Linyi, Shandong 276003, China
基金项目:Project supported by the National Natural Science Foundation of China (No.20272020).
摘    要:Optically pure S-5-hexadecanolide (1) has been easily prepared from readily available aldehyde 2 and cyclopentanone (3) using L-proline-catalyzed asymmetric aldol reactions as the key step.

关 键 词:乙醛  环戊酮  催化作用  化合物
收稿时间:2004-12-08
修稿时间:2004-12-082005-05-11

Asymmetric Synthesis of 5-Hexadecanolide
SUN Bin,ZHANG Chao-Xin,ZHANG Gui-Min,LI Ying,LI Yu-Lin,PENG Li-Zeng.Asymmetric Synthesis of 5-Hexadecanolide[J].Chinese Journal of Chemistry,2005,23(9):1228-1230.
Authors:SUN Bin  ZHANG Chao-Xin  ZHANG Gui-Min  LI Ying  LI Yu-Lin  PENG Li-Zeng
Abstract:Optically pure S‐5‐hexadecanolide ( 1 ) has been easily prepared from readily available aldehyde 2 and cyclopentanone ( 3 ) using L‐proline‐catalyzed asymmetric aldol reactions as the key step.
Keywords:5-hexadecanolide  Baeyer-Villiger oxidation  aldol reaction  L-proline
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