Issue 0, 1986

Intramolecular amidoseleniation of N-alkenyl imidates to N-heterocycles

Abstract

The reactions of N-alkenyl imidates with benzeneselenenyl chloride and bromide in chloroform at ambient temperature afford pyrrolidine and piperidine derivatives having a phenylseleno moiety in good to excellent yields under neutral conditions. The key step of this new reaction consists of an intramolecular carbon–nitrogen bond formation and a simultaneous carbon–oxygen bond fission.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1986, 1837-1843

Intramolecular amidoseleniation of N-alkenyl imidates to N-heterocycles

K. Terao, A. Toshimitsu and S. Uemura, J. Chem. Soc., Perkin Trans. 1, 1986, 1837 DOI: 10.1039/P19860001837

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