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

Research output: Contribution to journalArticle

14 Citations (Scopus)

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 languageEnglish
Pages (from-to)589-595
Number of pages7
JournalHeterocycles
Volume67
Issue number2
DOIs
Publication statusPublished - 1 Feb 2006

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Cycloaddition
Cycloaddition Reaction
Hot Temperature
Chemical activation
Pressure
naphthosultone

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety. / Rogachev, Victor O.; Filimonov, Victor D.; Fröhlich, Roland; Kataeva, Olga; Metz, Peter.

In: Heterocycles, Vol. 67, No. 2, 01.02.2006, p. 589-595.

Research output: Contribution to journalArticle

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