Enolate-mediated regioselective synthesis of 1,2,3-triazoles via azide-aldehydes or ketones [3+2]-cycloaddition reactions in aqueous phase

TitleEnolate-mediated regioselective synthesis of 1,2,3-triazoles via azide-aldehydes or ketones [3+2]-cycloaddition reactions in aqueous phase
Publication TypeJournal Article
Year of Publication2020
AuthorsTripathi, A, ,, Llop, J, Chavan, SP, Joshi, SM
JournalTetrahedron Letters
Volume61
Issue13
Pagination151662
Date PublishedMAR
Type of ArticleArticle
ISSN0040-4039
KeywordsAzides plus aldehydes or ketones, Click chemistry, triazoles, Water
Abstract

A synthetic route for the direct conversion of arylazides into the corresponding trizoles via phase transfer catalyst-assisted [3+2] cycloaddition reaction under basic conditions in aqueous medium is reported. This synthetic methodology, which offers high yields and excellent regioselectivity for varieties of triazoles at 100 degrees C for 24 h-48 h and this `greener' synthesis constitutes an alternative to the previously reported well established click reactions. Published by Elsevier Ltd.

DOI10.1016/j.tetlet.2020.151662
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

2.275

Divison category: 
Chemical Engineering & Process Development
Organic Chemistry

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