Expeditious and efficient annulation protocol for the synthesis of α,β-unsaturated δ-lactones from β-keto esters

dc.contributor.author Nangia, A.
dc.contributor.author Bheema Rao, P.
dc.date.accessioned 2022-03-27T09:36:08Z
dc.date.available 2022-03-27T09:36:08Z
dc.date.issued 1992-04-17
dc.description.abstract β-Keto esters 6a-3 are transformed into β-keto alcohols 7a-3, which are homologated to phosphonates 9a-e. Intramolecular Horner-Wadsworth-Emmons reaction affords δlactones 10a-d in excellent overall yields. © 1992.
dc.identifier.citation Tetrahedron Letters. v.33(17)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/S0040-4039(00)74216-X
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S004040390074216X
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13101
dc.subject Horner-Wadsworth-Emmons
dc.subject Intramoleculars
dc.subject Phosphonates
dc.subject °-Lactones
dc.subject β-Keto esters
dc.title Expeditious and efficient annulation protocol for the synthesis of α,β-unsaturated δ-lactones from β-keto esters
dc.type Journal. Article
dspace.entity.type
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