Studies on Horner-Wadsworth-Emmons reaction in base sensitive ketones: Synthesis of (-)-mitsugashiwalactone and formal synthesis of (+)-iridomyrmecin, (-)-isoiridomyrmecin and (+)-teucriumlactone

dc.contributor.author Nangia, A.
dc.contributor.author Prasuna, G.
dc.date.accessioned 2022-03-27T09:35:33Z
dc.date.available 2022-03-27T09:35:33Z
dc.date.issued 1996-01-01
dc.description.abstract The effect of different bases in promoting Horner-Wadsworth-Emmons (HWE) reaction on enolisable cyclopentanones is investigated. NaH is found to be suitable for the intermolecular reaction and DBU/LiCl is optimal for the intramolecular variation. The HWE approach is employed for the enantioselective synthesis of iridoid cyclopentapyranones of type-I (4, 16, 52) and type-II (5, 36).
dc.identifier.citation Tetrahedron. v.52(10)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/0040-4020(96)00023-3
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/0040402096000233
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13090
dc.title Studies on Horner-Wadsworth-Emmons reaction in base sensitive ketones: Synthesis of (-)-mitsugashiwalactone and formal synthesis of (+)-iridomyrmecin, (-)-isoiridomyrmecin and (+)-teucriumlactone
dc.type Journal. Article
dspace.entity.type
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