New cyclohexyl-based chiral auxiliaries: Enantioselective synthesis of α-hydroxy acids

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Krishna, Peddinti Rama
dc.date.accessioned 2022-03-27T09:04:18Z
dc.date.available 2022-03-27T09:04:18Z
dc.date.issued 1995-10-30
dc.description.abstract (1R,2R)-2-(4-tert-Butylphenoxy)cyclohexan-1-ol (5) and (1R,2R)-2-(4-phenylphenoxy)cyclohexan-1-ol (6) have been used for the first time as chiral auxiliaries. Addition of alkylzinc chlorides to the corresponding glyoxylates 5a, 6a, after hydrolysis, provided (R)-α-hydroxy acids in high optical purities. © 1995 Elsevier Science Ltd.
dc.identifier.citation Tetrahedron. v.51(44)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/0040-4020(95)00771-Y
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/004040209500771Y
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12367
dc.title New cyclohexyl-based chiral auxiliaries: Enantioselective synthesis of α-hydroxy acids
dc.type Journal. Article
dspace.entity.type
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