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

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DC Field	Value	Language
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
Appears in Collections:	Research articles (Dept of Chemistry)

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