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1-(SR)-对甲苯亚磺酰基-3-戊烯-2-酮与环戊二烯的不对称催化环加成反应
引用本文:裴文.1-(SR)-对甲苯亚磺酰基-3-戊烯-2-酮与环戊二烯的不对称催化环加成反应[J].高等学校化学学报,1999,20(2):251-253.
作者姓名:裴文
作者单位:延边大学化学系, 延吉 133002
基金项目:国家教育委员会留学回国人员基金
摘    要:前文曾报道了α-苯磺酰基-α,β-不饱和酮作为双烯体和亲双烯体所进行的不对称催化HeteroDiels-Alder反应1]和Diels-Alder反应2].为深入研究其反应机理,提出反应过渡态模型和鉴定环加成物构型.

关 键 词:对甲苯亚磺酰基  不对称催化  环加成反应  
收稿时间:1998-04-15

Lewis Acid-catalyzed Asymmetric Cycloaddition Reaction of 1-(SR)-p-Tolylsulfinyl-3-penten-2-one with Cyclopentadiene
PEI Wen.Lewis Acid-catalyzed Asymmetric Cycloaddition Reaction of 1-(SR)-p-Tolylsulfinyl-3-penten-2-one with Cyclopentadiene[J].Chemical Research In Chinese Universities,1999,20(2):251-253.
Authors:PEI Wen
Institution:Department of Chemistry, Yanbian University, Yanji, 133002
Abstract:The asymmetric cycloaddition reaction between 1(SR)ptolysulfinyl3penten2one( 1) and cyclopentadiene was performed by the catalysis of Lewis acids 2 . The diastereoselectivity dependent on the size of aryl substituent involved in the chiral ligands was discussed. The cycloadduct 3 was achieved in a high yield and a high optical purity. The absolute configuration of the cycloadduct 3 was confirmed.
Keywords:Tolysulfinyl  Asymmetric catalysis  Cycloaddition  
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