## Abstract The isomer‐pairs of the 2‐arylamino‐2‐thiazolines and ‐thiazines, carrying a methyl substituent on the nitrogen atom of the ring and outside the ring were synthesised by unambiguous routes. An IR and NMR investigation of these compounds revealed the fact that the NMR signal of the 2,6‐s
Carbon-13 n.m.r. investigation of 2-arylaminothiazolines and analogous thiazines, thiazepines and their amides
✍ Scribed by P. Sohár; G. Fehér; L. Toldy
- Book ID
- 102526341
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 286 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
The "C n.m.r. spectra of 2-arylaminothiazoline, -tbiazine and -thiazepine derivatives, and also those of some N-substituted isomeric pairs were recorded and assigned. The structure of the individual isomers, which as a result of contradictory spectroscopic data had earlier been ambiguous, was established. In addition, the tautomeric structure of some N-unsubstituted compounds was determined.
The structures of the 2-arylaminothiazolines ( n = 2), -thiazines ( n = 3), and -thiazepines ( n = 4), which can be characterized by the tautomeric structures l a (R = H) and l b (R=H), as well as the possible isomers of , R'
📜 SIMILAR VOLUMES
## Abstract ^13^C n.m.r. spectra have been measured for 39 compounds with branched structures including carboxylic acids, their methyl and ethyl esters, nitriles and chlorinated esters. The results obtained indicate that the ^13^ C n.m.r. technique is applicable to structure assignment of acids and
## Abstract The ^13^C n.m.r. spectra of the __N__‐methylated mono‐ and diazanaphthalenes have been recorded and analysed. It has been shown that __N__‐methylation as well as __N__‐protonation in cinnoline occur predominantly at the β‐nitrogen atom. __N__‐methylation and __N__‐protonation show a sim
## Abstract ^13^C n.m.r. spectra are reported for 1,2‐indandione, coumarandione and thionaphthenequinone in CDCl~3~ solution and for isatin in dimethyl sulphoxide solution. The chemical shifts are assigned and discussed in connection with the influence of the heteroatom on the dicarbonyl group and
## Abstract The influence of substituents in a new series of 2__H__‐thiopyrans, 2__H__‐thiopyran‐2‐ones (thiones) and their thiazine analogues is examined by means of carbon (^13^C) and nitrogen (^15^N) NMR. A linear relationship is shown to exist between the chemical shifts (δ~13C~ or δ~15N~) of t