Synthesis of fused nine-membered rings: A simple protocol for synthesis of [1,2,3]-triazolo-[1,4]-benzoxazonine frameworks from the Baylis-Hillman acetates

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Reddy, Bhavanam Sekhara
dc.contributor.author Lingam, Harathi
dc.date.accessioned 2022-03-27T09:01:04Z
dc.date.available 2022-03-27T09:01:04Z
dc.date.issued 2013-11-25
dc.description.abstract A simple and facile protocol for synthesis of tricyclic [1,2,3]-triazolo-[1,4]-benzoxazonine derivatives has been developed from the Baylis-Hillman acetates by treatment with sodium azide followed by heating the resulting azido-alkyne in toluene under reflux [Huisgen reaction (click reaction)] in the absence of any copper salt. © 2013 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron. v.69(47)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/j.tet.2013.09.056
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040402013014786
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12273
dc.subject [1,2,3]-Triazolo-[1,4]- benzoxazonines
dc.subject Azido-alkyne
dc.subject Baylis-Hillman reaction
dc.subject Click reaction
dc.title Synthesis of fused nine-membered rings: A simple protocol for synthesis of [1,2,3]-triazolo-[1,4]-benzoxazonine frameworks from the Baylis-Hillman acetates
dc.type Journal. Article
dspace.entity.type
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