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dc.contributor.author Masesane, I.
dc.contributor.author Steel, P.
dc.date.accessioned 2008-10-14T10:48:35Z
dc.date.available 2008-10-14T10:48:35Z
dc.date.issued 2004-06-21
dc.identifier.citation Masesane, I.B. and Steel, P.G .(2004) Stereoselective routes to 3-hydroxy and 3,4-dihydroxy derivatives of 2-aminocyclohexanecarboxylic acid, Tetrahedron Letters, Vol. 45, Issue 26, pp. 5007-5009 en
dc.identifier.issn 0040-4039
dc.identifier.uri http://hdl.handle.net/10311/235
dc.description.abstract The Diels-Alder adduct of ethyl (E)-3-nitroacrylate and furan provides a versatile template for the stereoselective synthesis of mono and dihydroxylated derivatives of 2-aminocyclohexanecarboxylic acid (ACHC). The hydroxylated ACHC derivatives can be considered to be useful building blocks for B-peptides. en
dc.language.iso en en
dc.publisher Elsevier Ltd; www.elsevier.com/locate/tetlet en
dc.subject Diels-Alder adduct en
dc.subject Cyclic b-amino acids en
dc.subject Reduction en
dc.subject Epoxidation en
dc.title Stereoselective routes to 3-hydroxy and 3,4-dihydroxy derivatives en
dc.type Article en


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