## Abstract β‐Lactam‐condensed saturated thiaazabicycles underwent ring transformation to give a new type of alicycle‐fused 3‐phenyl‐2‐methoxycarbonyl‐4,5‐dihydro‐1,4‐thiazepine. Oxidation of the __cis__ and __trans__ cyclohexane derivatives with perbenzoic acid furnished sulphones. The configurati
Synthesis and steric structure of alicycle-fused 1,3-thiazine-β-lactams
✍ Scribed by Pál Sohár; János Szabó; Lajos Simon; Gizella S. Talpas; Erzsébet Szücs; Gábor Bernáth
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 535 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
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 ^1^H and ^13^C NMR spectroscopy, including double resonance, DNOE and 2D HSC measurements.
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