Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety

Victor O. Rogachev, Victor D. Filimonov, Roland Fröhlich, Olga Kataeva, Peter Metz

The Kizhner Research Center

Research output: Contribution to journal › Article

Abstract

A range of novel γ- and enantiopure δ-sultams was prepared by intramolecular [4+2] cycloaddition of vinylsulfonamides with purely thermal activation and under high pressure.

Original language	English
Pages (from-to)	589-595
Number of pages	7
Journal	Heterocycles
Volume	67
Issue number	2
DOIs	https://doi.org/10.3987/COM-05-S(T)80
Publication status	Published - 1 Feb 2006

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ASJC Scopus subject areas

Organic Chemistry

Cite this

Rogachev, V. O., Filimonov, V. D., Fröhlich, R., Kataeva, O., & Metz, P. (2006). Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety. Heterocycles, 67(2), 589-595. https://doi.org/10.3987/COM-05-S(T)80

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AU - Metz, Peter

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Access to Document

10.3987/COM-05-S(T)80