New convenient synthesis of 1,4-benzothiazepines

L. Fodor, János Szabó, G. Bernáth, P. Sohár

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

New 1,4-benzothiazepine diastereomers 6a,b were prepared by ring expansion of the 1,3-benzothiazine derivative 1 and from 2-benzoylmethylthio-4,5-dimethoxybenzylamine hydrochloride (5) with benzaldehyde.

Original languageEnglish
Pages (from-to)753-756
Number of pages4
JournalTetrahedron Letters
Volume36
Issue number5
DOIs
Publication statusPublished - Jan 30 1995

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Derivatives
benzaldehyde

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

New convenient synthesis of 1,4-benzothiazepines. / Fodor, L.; Szabó, János; Bernáth, G.; Sohár, P.

In: Tetrahedron Letters, Vol. 36, No. 5, 30.01.1995, p. 753-756.

Research output: Contribution to journalArticle

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