Enantioselective synthesis of 2,3-diphenyl-1,4-butanediol via oxidative coupling of phenylacetic acid chiral 1,1'-bi-2-naphthyl ester using TiCl < inf > 4 < /inf > /Et < inf > 3 < /inf > N

dc.contributor.author Rao, Vutukuri Dharma
dc.contributor.author Periasamy, Mariappan
dc.date.accessioned 2022-03-27T09:10:30Z
dc.date.available 2022-03-27T09:10:30Z
dc.date.issued 1999-03-24
dc.description.abstract Oxidative coupling of phenylacetic acid ester of homochiral 1,1'-bi-2-naphthol 2 was achieved by reaction with TiCl4/Et3N to obtain the corresponding 2,3-diphenylsuccinic acid derivative 3, which on reduction using the NaBH4/I2 reagent gives homochiral 2,3-diphenyl-1,4-butanediol. X-Ray structural analysis was carried out for the compounds (R)-(+)-2 and (R,R,R)-(-)-3. Copyright (C) 2000.
dc.identifier.citation Tetrahedron Asymmetry. v.11(5)
dc.identifier.issn 09574166
dc.identifier.uri 10.1016/S0957-4166(00)00040-9
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0957416600000409
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12534
dc.title Enantioselective synthesis of 2,3-diphenyl-1,4-butanediol via oxidative coupling of phenylacetic acid chiral 1,1'-bi-2-naphthyl ester using TiCl < inf > 4 < /inf > /Et < inf > 3 < /inf > N
dc.type Journal. Article
dspace.entity.type
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