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
| 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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