Reaction engineering and photophysical studies of fully enriched: C -vinyl-1,2,3-triazoles

dc.contributor.author Surendra Reddy, G.
dc.contributor.author Ramachary, Dhevalapally B.
dc.date.accessioned 2022-03-27T09:37:10Z
dc.date.available 2022-03-27T09:37:10Z
dc.date.issued 2019-11-07
dc.description.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.
dc.identifier.citation Organic Chemistry Frontiers. v.6(21)
dc.identifier.issn 20524110
dc.identifier.uri 10.1039/c9qo00864k
dc.identifier.uri http://xlink.rsc.org/?DOI=C9QO00864K
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13121
dc.title Reaction engineering and photophysical studies of fully enriched: C -vinyl-1,2,3-triazoles
dc.type Journal. Article
dspace.entity.type
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