Issue 22, 1995

Highly selective asymmetric intramolecular selenocyclisation

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2321-2322

Highly selective asymmetric intramolecular selenocyclisation

Y. Nishibayashi, S. K. Srivastava, H. Takada, S. Fukuzawa and S. Uemura, J. Chem. Soc., Chem. Commun., 1995, 2321 DOI: 10.1039/C39950002321

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