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Diastereoselective Michael Addition of (4'S)-Ethyl-3-(2',2'-Dimethyl-1',3'- dioxolan-4'-yl) acrylate with Furyl Lithium
作者姓名:Dong Mei HAN  Xun Tian JIANG  Jian Hong CHEN  Bin WANG  Dong Lu BAI* Shanghai Institute of Meteria Medica  Shanghai Institutes for Biological Sciences  Chinese Academy of Sciences  Shanghai
作者单位:Dong Mei HAN,Xun Tian JIANG,Jian Hong CHEN,Bin WANG,Dong Lu BAI* Shanghai Institute of Meteria Medica,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Shanghai 200031
摘    要:Recently we reported that the diastereoselective intramolecular 4+3] cycloaddition of 4 led to the formation of cycloadduct 5 as the only isolated isomer in 50% yield. The chiral C-3 of compound 4 could be used to direct the stereochemical course of 4+3] cycloaddition enabling the control of the relative stereochemistry between three contiguous asymmetric centers in adduct 51. The stereogenic center at C-3 of 4 was constructed by the asymmetric Michael addition of (, (-unsaturated ester 2 w…


Diastereoselective Michael Addition of (4'S)-Ethyl-3-(2',2'-Dimethyl-1',3'- dioxolan-4'-yl) acrylate with Furyl Lithium
Dong Mei HAN,Xun Tian JIANG,Jian Hong CHEN,Bin WANG,Dong Lu BAI* Shanghai Institute of Meteria Medica,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Shanghai .Diastereoselective Michael Addition of (4''''S)-Ethyl-3-(2'''',2''''-Dimethyl-1'''',3''''- dioxolan-4''''-yl) acrylate with Furyl Lithium[J].Chinese Chemical Letters,2001(5).
Authors:Dong Mei HAN  Xun Tian JIANG  Jian Hong CHEN  Bin WANG  Dong Lu BAI
Institution:Dong Mei HAN,Xun Tian JIANG,Jian Hong CHEN,Bin WANG,Dong Lu BAI* Shanghai Institute of Meteria Medica,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Shanghai 200031
Abstract:
Keywords:Michael addition  configuration determination  syn addition  
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