Reductive formation of 1,5-benzothiazepines

A. Lévai, Gábor Tóth, Tímea Gondos, J. Jekó́, D. I. Brahmbhatt

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

An unprecedented formation of a new type of 1,5-benzothiazepines with exocyclic double bond at position 4 has been achieved by the reaction of 3-aryl-1-(3-coumarinyl)propen-1-ones with 2-aminothiophenol.

Original languageEnglish
Pages (from-to)1319-1324
Number of pages6
JournalHeterocycles
Volume68
Issue number7
DOIs
Publication statusPublished - Jul 1 2006

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2-aminothiophenol
1,5-benzothiazepine

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Reductive formation of 1,5-benzothiazepines. / Lévai, A.; Tóth, Gábor; Gondos, Tímea; Jekó́, J.; Brahmbhatt, D. I.

In: Heterocycles, Vol. 68, No. 7, 01.07.2006, p. 1319-1324.

Research output: Contribution to journalArticle

Lévai, A, Tóth, G, Gondos, T, Jekó́, J & Brahmbhatt, DI 2006, 'Reductive formation of 1,5-benzothiazepines', Heterocycles, vol. 68, no. 7, pp. 1319-1324. https://doi.org/10.3987/COM-06-10702
Lévai, A. ; Tóth, Gábor ; Gondos, Tímea ; Jekó́, J. ; Brahmbhatt, D. I. / Reductive formation of 1,5-benzothiazepines. In: Heterocycles. 2006 ; Vol. 68, No. 7. pp. 1319-1324.
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