Highly selective asymmetric intramolecular selenocyclisation

Y. Nishibayashi, S. Srivastava, H. Takada, S. Fukuzawa, S. Uemura
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引用次数: 30

Abstract

Asymmetric intramolecular selenocyclisation of alkenoic acids, alkenols and olefinic urethanes using chiral ferrocenylselenenyl cations proceeds smoothly to give the corresponding lactones, cyclic ethers and nitrogen-heterocyclic compounds, respectively, in moderate yields with very high diastereoselectivities.
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高选择性不对称分子内硒环化
利用手性二茂铁亚硒烯基阳离子对烯酸、烯醇和烯烃氨基甲酸进行不对称的分子内硒环化反应,分别得到相应的内酯、环醚和氮杂环化合物,产率中等,具有很高的非对映选择性。
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