Synthesis and steric structure of alicycle‐fused 1,3‐thiazine‐β‐lactams

P. Sohár, János Szabó, Lajos Simon, Gizella S. Talpas, Erzsébet Szücs, G. Bernáth

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

2 + 2‐Cycloaddition reactions of cis‐ and trans‐cyclopenta‐, ‐cyclohexa‐ and ‐cyclohepta‐ and trans‐cycloocta [e]‐2‐phenyl‐4H‐1,3‐thiazines gave new types of hydrated tricyclic 1,3‐thiazino‐β‐lactam derivatives having the 2‐phenyl substituent and H‐9 in cis positions. The configurations and conformations of the new compounds were determined by 1H and 13C NMR spectroscopy, including double resonance, DNOE and 2D HSC measurements.

Original languageEnglish
Pages (from-to)687-692
Number of pages6
JournalMagnetic Resonance in Chemistry
Volume29
Issue number7
DOIs
Publication statusPublished - 1991

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Nuclear magnetic resonance spectroscopy
Conformations
Derivatives

Keywords

  • H and C NMR spectra
  • 2D‐HSC
  • Alicycle‐fused 1,3‐thiazino‐β‐lactams
  • Conformational analysis
  • Double resonance DNOF
  • Synthesis

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

Cite this

Synthesis and steric structure of alicycle‐fused 1,3‐thiazine‐β‐lactams. / Sohár, P.; Szabó, János; Simon, Lajos; Talpas, Gizella S.; Szücs, Erzsébet; Bernáth, G.

In: Magnetic Resonance in Chemistry, Vol. 29, No. 7, 1991, p. 687-692.

Research output: Contribution to journalArticle

Sohár, P. ; Szabó, János ; Simon, Lajos ; Talpas, Gizella S. ; Szücs, Erzsébet ; Bernáth, G. / Synthesis and steric structure of alicycle‐fused 1,3‐thiazine‐β‐lactams. In: Magnetic Resonance in Chemistry. 1991 ; Vol. 29, No. 7. pp. 687-692.
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AU - Szücs, Erzsébet

AU - Bernáth, G.

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