Reaction engineering and photophysical studies of fully enriched: C -vinyl-1,2,3-triazoles
Reaction engineering and photophysical studies of fully enriched: C -vinyl-1,2,3-triazoles
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Date
2019-11-07
Authors
Surendra Reddy, G.
Ramachary, Dhevalapally B.
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Abstract
For the first time, an enolate-mediated organocatalytic fluorogenic formal [3 + 2]-cycloaddition of (E)-1,4-diarylbut-3-en-1-ones and aryl azides is reported. The mild metal-free catalytic conditions of this reaction allowed us to synthesize a library of pure fluorescent coumarin-triazole dyes. It is an efficient formal [3 + 2]-cycloaddition for the synthesis of fully decorated C-vinyl-1,2,3-triazoles with excellent outcomes with reference to the rate, yield, selectivity, operation simplicity, substrate scope, and photophysical applications.
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Organic Chemistry Frontiers. v.6(21)