Pig liver acetone powder (PLAP) mediated enantioselective synthesis of cyclic ketones

dc.contributor.author Basavaiah, D.
dc.contributor.author Krishna, P. Rama
dc.date.accessioned 2022-03-27T09:04:28Z
dc.date.available 2022-03-27T09:04:28Z
dc.date.issued 1995-02-01
dc.description.abstract Pig liver acetone powder (PLAP) hydrolyzes 2-substituted 1-acetoxycycloalk-1-enes providing the desired chiral ketones in 10–42% ee. © 1995, Taylor & Francis Group, LLC. All rights reserved.
dc.identifier.citation Synthetic Communications. v.25(3)
dc.identifier.issn 00397911
dc.identifier.uri 10.1080/00397919508011358
dc.identifier.uri http://www.tandfonline.com/doi/abs/10.1080/00397919508011358
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12371
dc.title Pig liver acetone powder (PLAP) mediated enantioselective synthesis of cyclic ketones
dc.type Journal. Article
dspace.entity.type
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