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The reactions of 1,2,3-triazolo[1,5-a]pyridine with electrophiles

✍ Scribed by Jones, Gurnos; Sliskovic, D. Robert; Foster, Beverley; Rogers, John; Smith, Anthony K.; Wong, Mee Yin; Yarham, Anthony C.

Book ID
121215142
Publisher
Royal Society of Chemistry
Year
1981
Weight
474 KB
Category
Article
ISSN
1472-7781

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πŸ“œ SIMILAR VOLUMES

Triazolopyridines. Part 8.1 Nucleophilic
Triazolopyridines. Part 8.1 Nucleophilic substitution reactions of 5-bromo[1,2,3]triazolo[5,1-a]isoquinoline and 7-bromo[1,2,3]-triazolo[1,5-a]pyridine
✍ Belen Abarca; Fatemeh Mojarred; Gurnos Jones; Caroline Phillips; Nadine Ng; Jona πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 French βš– 721 KB

Nucleophilic substitution of 5-bromotriazoloisoquinoline (3) and of 7-bromo-3-methyltriazolopyridine (6) proceeds readily to give a range of 5-substituted triazoloisoquinolines (4a)-(4e), and of 7-substituted triazolopyridines (7a)-(7h) respectively. Triazoloisoquinolines have been converted into 1,