Azide-acetonitrile "click" reaction triggered by Cs < inf > 2 < /inf > CO < inf > 3 < /inf > : The atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles

dc.contributor.author Krishna, Patoju M.
dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Peesapati, Sruthi
dc.date.accessioned 2022-03-27T09:39:18Z
dc.date.available 2022-03-27T09:39:18Z
dc.date.issued 2015-01-01
dc.description.abstract Medicinally important 5-amino-1,2,3-triazoles were synthesized using a novel Cs2CO3-catalyzed azide-acetonitrile[3 + 2]-cycloaddition. Aryl azides and aryl acetonitriles were employed in this transformation resulting in excellent yields with high regioselectivity.
dc.identifier.citation RSC Advances. v.5(76)
dc.identifier.uri 10.1039/c5ra12308a
dc.identifier.uri http://xlink.rsc.org/?DOI=C5RA12308A
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13161
dc.title Azide-acetonitrile "click" reaction triggered by Cs < inf > 2 < /inf > CO < inf > 3 < /inf > : The atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles
dc.type Journal. Article
dspace.entity.type
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