## Abstract The conformational preferences in solution of eight new openβchain and cyclic aromatic sulphides containing pyridine or 1,3,4βthiadiazole units have been investigated, parallel to those of some structurally related phenyl sulphides, by means of ^1^H NMR spectroscopy. The results obtaine
β¦ LIBER β¦
Synthesis, spectral properties and conformational preferences of macrocyclic compounds containing 2,5-dithio-1,3,4-thiadiazole subunits
β Scribed by F. Bottino; S. Pappalardo
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 614 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4020
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