Dimethyl sulfide induced [3 + 2] annulation strategy: An efficient synthesis of functionalized dihydropyrazole derivatives using the Baylis-Hillman bromides

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Roy, Suparna
dc.date.accessioned 2022-03-27T09:01:50Z
dc.date.available 2022-03-27T09:01:50Z
dc.date.issued 2008-05-01
dc.description.abstract Baylis-Hlllman bromides have been successfully employed as a valuable source of 1,3-dipoles for cycloaddition onto dialkyl azodicarboxylates (dipolarophiles) under the influence of dimethyl sulfide and potassium carbonate to provide functionalized dihydropyrazole derivatives in a simple one-pot [3 + 2] annulation strategy. © 2008 American Chemical Society.
dc.identifier.citation Organic Letters. v.10(9)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/ol800424v
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ol800424v
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12296
dc.title Dimethyl sulfide induced [3 + 2] annulation strategy: An efficient synthesis of functionalized dihydropyrazole derivatives using the Baylis-Hillman bromides
dc.type Journal. Article
dspace.entity.type
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