First enantioselective synthesis of mikanecic acid via Diels-Alder cycloaddition mediated construction of chiral vinylic quaternary center

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Pandiaraju, Subramanian
dc.contributor.author Sarma, Pakala K.S.
dc.date.accessioned 2022-03-27T09:04:39Z
dc.date.available 2022-03-27T09:04:39Z
dc.date.issued 1994-06-13
dc.description.abstract Chiral mikanecic acid (1) was synthesized in 74% enantiomeric purity (92% ee after crystallization) via asymmetric Diels-Alder reaction of a novel in situ generated chiral 1,3-butadiene-2-carboxylate (A). © 1994.
dc.identifier.citation Tetrahedron Letters. v.35(24)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/S0040-4039(00)73158-3
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403900731583
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12376
dc.title First enantioselective synthesis of mikanecic acid via Diels-Alder cycloaddition mediated construction of chiral vinylic quaternary center
dc.type Journal. Article
dspace.entity.type
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