A Novel Tandem Asymmetric Michael Addition-Elimination Reaction  

A Novel Tandem Asymmetric Michael Addition-Elimination Reaction

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作  者:陈庆华 耿哲 

机构地区:[1]Department of Chemistry, Beijing Normal University, Beijing 100875, PRC

出  处:《Chinese Science Bulletin》1993年第9期791-792,共2页

基  金:Project supported by the National Natural Science Foundation of China.

摘  要:The synthesis and properties of γ-substituted butenolides have recently attracted much attention in the field of organic chemistry owing to their unique carbon skeleton of 2(5H)-furanone which is widely present in many natural products and shows interesting antiobiotic activities as well as their important acting as a synthetic intermediate. We have published as a preliminary communication, an optically pure and high yielding syn-

关 键 词:substituted SKELETON preliminary optically YIELDING dichloro CONJUGATE ACTING THIOL catalysis 

分 类 号:N[自然科学总论]

 

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