New methods of resolution and purification of racemic and diastereomeric amino alcohol derivatives using boric acid and chiral 1,1′-bi-2-naphthol

dc.contributor.author Periasamy, M.
dc.contributor.author Kumar, N. S.
dc.contributor.author Sivakumar, S.
dc.contributor.author Rao, V. D.
dc.contributor.author Ramanathan, C. R.
dc.contributor.author Venkatraman, L.
dc.date.accessioned 2022-03-27T09:09:44Z
dc.date.available 2022-03-27T09:09:44Z
dc.date.issued 2001-06-01
dc.description.abstract Resolution of the racemic amino alcohol derivatives 1-6 is readily achieved to obtain enantiomerically enriched compounds using chiral 1,1′-bi-2-naphthol and boric acid in solvents such as CH3-CN, THF, and MeOH. Purification of the diastereomeric mixture 7 has also been carried out following this method. The corresponding intermediate ammonium borate complexes were also characterized by X-ray diffraction methods.
dc.identifier.citation Journal of Organic Chemistry. v.66(11)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo0057755
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jo0057755
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12514
dc.title New methods of resolution and purification of racemic and diastereomeric amino alcohol derivatives using boric acid and chiral 1,1′-bi-2-naphthol
dc.type Journal. Article
dspace.entity.type
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