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Semiemperical calculations in the prediction of regioselectivity of cyclopentenone [2+2] photocycloaddition

Kraim Khaireddine, Khatmi Djameleddine


The [2+2] photocycloaddition of enone such as cyclopentenone to substituted chiral ethylene as alkene has been studied using semiemperical methods (AM1, PM3 and MNDO) were applied. The results showed that, the reaction occurs in the triplet state of enone and the ground state of alkene, also, we have deduced that the regioselectivity can be explained assuming that the [2+2] photocycloaddition reaction is frontier orbital controlled.


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  • 中国社会科学院
  • 谷歌学术
  • 打开 J 门
  • 中国知网(CNKI)
  • 引用因子
  • 宇宙IF
  • 电子期刊图书馆
  • 研究期刊索引目录 (DRJI)
  • 秘密搜索引擎实验室
  • ICMJE

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