Transition metal, azide, and oxidant-free homo- and heterocoupling of ambiphilic tosylhydrazones to the regioselective triazoles and pyrazoles

TitleTransition metal, azide, and oxidant-free homo- and heterocoupling of ambiphilic tosylhydrazones to the regioselective triazoles and pyrazoles
Publication TypeJournal Article
Year of Publication2017
AuthorsPanda, S, Maity, P, Manna, D
JournalOrganic Letters
Volume19
Issue7
Pagination1534-1537
Date PublishedAPR
Type of ArticleArticle
AbstractWith N-tosylhydrazone as an ambiphilic reagent, an unprecedented cyclization reaction of two identical or different tosylhydrazones has been developed to access various 4,5-disubstituted-2H-triazoles under transition metal, azide, and oxidant-free conditions. A mechanistic.rationalization study led to the identification of several electronically diverse unsaturated systems for regioselective synthesis of 1- and 2-substituted 1,2,3-triazoles and pyrazoles.
DOI10.1021/acs.orglett.7b00313
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)6.732
Divison category: 
Organic Chemistry

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