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ENANTIOSELECTIVE SYNTHESIS OF CINNAMYL-1-PHENYL-2-PROPENYL ETHER - A METABOLITE OF MARINE GREEN ALGAL SPECIES CAULERPA-RACEMOSA

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dc.contributor.author Mallavadhani, U.V.
dc.contributor.author Rao, Y.R.
dc.date.accessioned 2018-10-01T12:19:42Z
dc.date.available 2018-10-01T12:19:42Z
dc.date.issued 1994
dc.identifier.citation Tetrahedron-Asymmetry, 5(1), 1994: 23-26
dc.identifier.issn 0957-4166
dc.identifier.uri http://ore.immt.res.in/handle/2018/453
dc.description.abstract The enantioselective synthesis of title compound has been achieved using a new enzyme acyl system and a mild PT catalysed etherification. The absolute configuration of natural compound has been established as R-(+) by (1)HNMR analysis of MTPA esters of the intermediate carbinols.
dc.language en
dc.publisher Elsevier
dc.relation.isreferencedby SCI
dc.rights Copyright [1994]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subject Chemical Sciences
dc.subject Chemical Sciences
dc.subject Chemical Sciences
dc.title ENANTIOSELECTIVE SYNTHESIS OF CINNAMYL-1-PHENYL-2-PROPENYL ETHER - A METABOLITE OF MARINE GREEN ALGAL SPECIES CAULERPA-RACEMOSA
dc.type Journal Article
dc.affiliation.author CSIR-IMMT, Bhubaneswar 751013, Odisha, India


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