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Facile Selective Diels-Alder Reactions of Chiral 5, 5-Dimethyl-4,6-Mathano-2-Methoxycarbonyl-2-Cyclohexenone. Application to the Total Synthesis of Qinghaosu
作者姓名:LIU Hsing-Jang  CHEW Sew-Yeu  YEH Wen-Lung
作者单位:LIU Hsing-Jang;CHEW Sew-Yeu;YEH Wen-Lung Department of Chemistry,The University of Alberta,Edmonton,Alberta,Canada T6G 2G2
摘    要:Starting from (--)-β-pinene,an efficient synthesis of qinghaosu (8) in natural form hasbeen accomplished. The synthesis involves keto ester 7 as a key intermediate which is conveniently pre-pared using the Diels-Alder chemistry developed in our laboratory.

关 键 词:(-)-β-Pinene  Diels-Alder  reaction  synthesis  of  qinghaosu

Facile Selective Diels-Alder Reactions of Chiral 5, 5-Dimethyl-4, 6-Mathano-2-Methoxycarbonyl-2-Cyclohexenone. Application to the Total Synthesis of Qinghaosu
LIU Hsing-Jang,CHEW Sew-Yeu,YEH Wen-Lung.Facile Selective Diels-Alder Reactions of Chiral 5, 5-Dimethyl-4,6-Mathano-2-Methoxycarbonyl-2-Cyclohexenone. Application to the Total Synthesis of Qinghaosu[J].Chinese Journal of Organic Chemistry,1993(3).
Authors:LIU Hsing-Jang  CHEW Sew-Yeu  YEH Wen-Lung
Institution:LIU Hsing-Jang,CHEW Sew-Yeu,YEH Wen-Lung Department of Chemistry,The University of Alberta,Edmonton,Alberta,Canada T6G 2G2
Abstract:
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