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Article: The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution

TitleThe synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution
Authors
Issue Date1979
Citation
Tetrahedron Letters, 1979, v. 20, n. 28, p. 2629-2632 How to Cite?
AbstractThe rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of (R)- and (S)-α-phenylethylammonium perchlorate. © 1979.
Persistent Identifierhttp://hdl.handle.net/10722/332280
ISSN
2023 Impact Factor: 1.5
2023 SCImago Journal Rankings: 0.323

 

DC FieldValueLanguage
dc.contributor.authorAndrews, David G.-
dc.contributor.authorAshton, Peter R.-
dc.contributor.authorLaidler, Dale A.-
dc.contributor.authorStoddart, J. Fraser-
dc.contributor.authorWolstenholme, John B.-
dc.date.accessioned2023-10-06T05:10:15Z-
dc.date.available2023-10-06T05:10:15Z-
dc.date.issued1979-
dc.identifier.citationTetrahedron Letters, 1979, v. 20, n. 28, p. 2629-2632-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10722/332280-
dc.description.abstractThe rationale behind designing and the approach to synthesising chiral crown ethers incorporating three trigonally-disposed carbohydrate residues is presented as a prelude to attaining chiral discrimination in the complexation of (R)- and (S)-α-phenylethylammonium perchlorate. © 1979.-
dc.languageeng-
dc.relation.ispartofTetrahedron Letters-
dc.titleThe synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/S0040-4039(01)86369-3-
dc.identifier.scopuseid_2-s2.0-0000840456-
dc.identifier.volume20-
dc.identifier.issue28-
dc.identifier.spage2629-
dc.identifier.epage2632-

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