Theoretical Studies on the Mechanisms of [2+2] Cycloaddition Reactions

被引:0
|
作者
Fang Decai [1 ]
机构
[1] Beijing Normal Univ, Coll Chem, Beijing 100875, Peoples R China
关键词
cycloaddition reaction; cumulenes; diradical mechanism; concerted mechanism; zwitterion; KETENE-IMINE CYCLOADDITION; DENSITY-FUNCTIONAL THEORY; STAUDINGER REACTION; BETA-LACTAMS; AB-INITIO; KETENIMINIUM SALTS; ASYMMETRIC-SYNTHESIS; ALPHA-AMINO; INTRAMOLECULAR CYCLOADDITIONS; ENANTIOMERICALLY PURE;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
[2 + 2] cycloaddition reaction is one type of the most important reactions in the field of organic chemistry, and the mechanisms' of [2 + 2] cycloaddition reactions are always hot topic both for experimental and theoretical researchers. In this paper, three types of [2 + 2] cycloaddition reactions, including that of simple olefins or alkynes, cumulenes, Th compounds, have been classified and reviewed. The obtained results indicate that the cycloaddition reactions involving simple olefins or alkynes are proceeding in diradical mechanism generally, and the others are proceeding in either concerted or zwitterion mechanism. All of which have been elucidated with frontier molecular orbital interactions.
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页码:879 / 885
页数:7
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