HIGHLY SELECTIVE ASYMMETRIC INTRAMOLECULAR SELENOCYCLISATION

被引：68

作者：

NISHIBAYASHI, Y

SRIVASTAVA, SK

TAKADA, H

FUKUZAWA, S

UEMURA, S

机构：

[1] KYOTO UNIV,GRAD SCH ENGN,DIV ENERGY & HYDROCARBON CHEM,SAKYO KU,KYOTO 60601,JAPAN

[2] CHUO UNIV,FAC SCI & ENGN,BUNKYO KU,TOKYO 112,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1995年 / 22期

关键词：

D O I：

10.1039/c39950002321

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

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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收藏

页码：2321 / 2322

页数：2

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