Organocatalytic Vinyl Azide-Carbonyl [3+2] Cycloaddition: High-Yielding Synthesis of Fully Decorated N-Vinyl-1,2,3-Triazoles

dc.contributor.author	Ramachary, Dhevalapally B.
dc.contributor.author	Reddy, G. Surendra
dc.contributor.author	Peraka, Swamy
dc.contributor.author	Gujral, Jagjeet
dc.date.accessioned	2022-03-27T09:38:30Z
dc.date.available	2022-03-27T09:38:30Z
dc.date.issued	2017-01-23
dc.description.abstract	For the first time, an enolate-mediated organocatalytic vinyl azide-carbonyl [3+2] cycloaddition (OrgVACC) of various ketones/aldehydes with vinyl azides is reported. It is an efficient intermolecular reaction with excellent outcomes with reference to rate, yield, selectivity, operational simplicity, substrate scope, catalyst simplicity, and vast applications.
dc.identifier.citation	ChemCatChem. v.9(2)
dc.identifier.issn	18673880
dc.identifier.uri	10.1002/cctc.201601317
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/cctc.201601317
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/13146
dc.subject	aldehydes
dc.subject	azides
dc.subject	cycloaddition
dc.subject	ketones
dc.subject	organocatalysis
dc.title	Organocatalytic Vinyl Azide-Carbonyl [3+2] Cycloaddition: High-Yielding Synthesis of Fully Decorated N-Vinyl-1,2,3-Triazoles
dc.type	Journal. Article
dspace.entity.type

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