Stereoselective routes to 3-hydroxy and 3,4-dihydroxy derivatives

Please use this identifier to cite or link to this item: http://hdl.handle.net/10311/235

Title:	Stereoselective routes to 3-hydroxy and 3,4-dihydroxy derivatives
Authors:	Masesane, I. Steel, P.
Keywords:	Diels-Alder adduct Cyclic b-amino acids Reduction Epoxidation
Issue Date:	21-Jun-2004
Publisher:	Elsevier Ltd; www.elsevier.com/locate/tetlet
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
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.
URI:	http://hdl.handle.net/10311/235
ISSN:	0040-4039
Appears in Collections:	Research articles (Dept of Chemistry)

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