## Abstract Ten new 1,2,4‐triazolo[3,4‐__b__]‐1,3,4‐thiadiazole derivatives were synthesized and their NMR spectra were analyzed by 1D and 2D NMR techniques (gCOSY, gHMBC, gHMQC). Copyright © 2001 John Wiley & Sons, Ltd.
13C NMR study of some derivatives of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and isosydnones
✍ Scribed by Gérard Aranda; Michèle Dessolin; Michel Golfier; Marie-George Guillerez
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 493 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The assignment of all ring carbons of 37 derivatives of 1,3,4‐oxa‐ or thiadiazoles and of seven isosydnones is described. In some cases, ^13^C‐labelled compounds were used. The analysis of substituent effects and the calculation of charge densities of some of the derivatives suggest that the two nitrogen atoms form a protective screen against electron perturbation and play the role of an ‘electronic buffer’. A notable variation of chemical shifts could be observed only when oxygen is replaced by sulphur.
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Jordan 1,3,5-Tris(5-substituted-1,3,4-oxadiazol-2-yl)benzenes were prepared by the dehydration of the corresponding hydrazides. The structures of these compounds were elucidated by IR, 1H and 13C NMR spectroscopy.
## Abstract Dehydration of __N__,__N__′‐diacylalkanedioic acid dihydrazides with phosphoryl chloride gave 5,5′‐disubstituted‐2,2′‐(1,__n__‐alkanediyl)bis‐1,3,4‐oxadiazoles. The structures of these compounds were elucidated by ^1^H, ^13^C NMR, UV and IR spectroscopy.
## Abstract The ^13^C NMR spectra of four pairs of 1,3,4‐thiadiazole/thiadiazoline isomers have been recorded using broad band and off‐resonance proton decoupling techniques and in the coupled mode. Differences in the chemical shifts of the heterocyclic ring and the carbonyl carbons allow identific
## Abstract Several 1‐(1‐aryl‐1,4‐dihydro‐3‐carboxy‐6‐methylpyridazin‐4‐one)‐4‐aryl thio‐semicarbazides and their corresponding oxadiazole, thiadiazole and triazole derivatives were prepared and characterized by their spectral data. The preliminary biological tests showed that some new compounds ex