## 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
Synthesis and steric structure of cis- and trans-alicycle-fused dihydrothiazepines
✍ Scribed by P. Sohár; K. Újszászy; J. Szabó; L. Simon; G. S. Talpas; L. Fodor; G. Bernáth
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 459 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
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 configurations and conformations of the new compounds were confirmed by ^1^H and ^13^C NMR spectroscopy, making use of DR, DNOE, DEPT and 2D HSC measurements.
📜 SIMILAR VOLUMES
## Abstract The synthesis of __cis__‐ and __trans__‐2‐(diethylaminomethyl)‐cyclohexanols and their structural assignments by NMR using the shift reagent Eu(dpm)~3~ are described. The correlation of the induced shifts with the equation Δν = __K__(3 cos^2^θ – 1)__r__^−3^, assuming an EuO distance of