Reversible photodimerization of 2-methyl-s-triazolo[1,5-a]pyridines
β Scribed by T. Nagano; M. Hirobe; M. Itoh; T. Okamoto
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 223 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
The major decomposition pathway involved in the fragmentation of derivatives of the title ring systems was the loss of RCN from the five-membered ring, except when this ring had a 3-amino, 3-hydroxyl or 3-mercapto substituent. In these cases, the exocyclic substituent and at least one nitrogen atom
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## Abstract magnified image Twentyβthree 2β(substituted)phenylβ1,2,4βtriazolo[1,5β__a__]pyridines have been synthesized by cycloadditison reaction between __N__βamino methylpyridinium mesitylenesulfonates and substituted benzonitriles under the presence of potassium hydroxide at room temperature.