Enantiodivergent syntheses of (r)- and (s)-3,5-dimethylcyclohex-2-en-1-ones from (r)-pulegone

dc.contributor.author Nangia, A.
dc.contributor.author Prasuna, G.
dc.date.accessioned 2022-03-27T09:35:49Z
dc.date.available 2022-03-27T09:35:49Z
dc.date.issued 1994-07-01
dc.description.abstract R-(+)-pulegone (1) is transformed to (R)-5-roethy1-2-(phenylsulfiny1)cyclohexanone (5) (65%, 3 steps). Sulfoxide 5 is converted to R-(-)-3,5-dimethy1 eye 1ohex-2-en-1-one (4) (53%, 4 steps) and S-(+)-4 (26%, 3 steps). © 1994, Taylor & Francis Group, LLC. All rights reserved.
dc.identifier.citation Synthetic Communications. v.24(14)
dc.identifier.issn 00397911
dc.identifier.uri 10.1080/00397919408010206
dc.identifier.uri http://www.tandfonline.com/doi/abs/10.1080/00397919408010206
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13095
dc.title Enantiodivergent syntheses of (r)- and (s)-3,5-dimethylcyclohex-2-en-1-ones from (r)-pulegone
dc.type Journal. Article
dspace.entity.type
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