Enantioselective synthesis of α- and β-hydroxy acids using trans-2-phenylcyclohexan-1-ol-as chiral auxiliary

dc.contributor.author	Basavaiah, D.
dc.contributor.author	Bharathi, T. K.
dc.date.accessioned	2022-03-27T09:05:06Z
dc.date.available	2022-03-27T09:05:06Z
dc.date.issued	1991-07-08
dc.description.abstract	trans-2-Phenylcyclohexanol has been used as a chiral auxiliary for the preparation of α- and β-hydroxy acids in 85-100% and 11-89% enantiomeric purities respectively. © 1991.
dc.identifier.citation	Tetrahedron Letters. v.32(28)
dc.identifier.issn	00404039
dc.identifier.uri	10.1016/S0040-4039(00)92724-2
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040403900927242
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12388
dc.subject	alkylzinc chloride
dc.subject	chiral auxiliary
dc.subject	Reformatsky reaction
dc.subject	trans-2-phenylcyclohexanol
dc.subject	α- and β-hydroxy acids.
dc.title	Enantioselective synthesis of α- and β-hydroxy acids using trans-2-phenylcyclohexan-1-ol-as chiral auxiliary
dc.type	Journal. Article
dspace.entity.type

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