Photoinduced multicomponent regioselective synthesis of 1,4,5-trisubstituted-1,2,3-triazoles: transition metal-, azide- and oxidant-free protocol

TitlePhotoinduced multicomponent regioselective synthesis of 1,4,5-trisubstituted-1,2,3-triazoles: transition metal-, azide- and oxidant-free protocol
Publication TypeJournal Article
Year of Publication2021
AuthorsAllaka, BSai, Basavoju, S, Krishna, GRama
JournalAdvanced Synthesis & Catalysis
Volume363
Issue14
Pagination3560-3565
Date PublishedJUL
Type of ArticleArticle
ISSN1615-4150
Keywords1, 2, 3-triazoles, 4, 5-trisubstituted-1, azide- and oxidant free protocol, Cycloaddition, milder reaction conditions, molecular diversity, Multicomponent reaction, Regioselectivity, transition metal-
AbstractA transition metal- and azide-free approach is explored to synthesize 1,4,5-trisubstituted-1,2,3-triazoles under sunlight. The reaction proceeds via C-N and N-N bond formations. These regioselective 1,2,3-triazoles are obtained from isatin Schiff bases, benzaldehydes and tosylhydrazine in the presence of base. This protocol offers the structurally diverse 1,2,3-triazole derivatives with 75-90% yields.
DOI10.1002/adsc.202100321
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)5.837
Divison category: 
Organic Chemistry

Add new comment