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Deprotonative Magnesation and Cadmation of [1,2,3]Triazolo[1,5- a ]pyridines

✍ Scribed by Bentabed-Ababsa, Ghenia; Blanco, Fernando; Derdour, Aïcha; Mongin, Florence; Trécourt, François; Quéguiner, Guy; Ballesteros, Rafael; Abarca, Belén


Book ID
126146513
Publisher
American Chemical Society
Year
2009
Tongue
English
Weight
197 KB
Volume
74
Category
Article
ISSN
0022-3263

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Triazolopyridines. Part 8.1 Nucleophilic
✍ Belen Abarca; Fatemeh Mojarred; Gurnos Jones; Caroline Phillips; Nadine Ng; Jona 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 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,