Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl b-amino acid derivatives

Please use this identifier to cite or link to this item: http://hdl.handle.net/10311/325

Title:	Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl b-amino acid derivatives
Authors:	Chola, J. Masesane, I.B.
Keywords:	tetrahydroxy derivatives Stereoselective syntheses furan maleic anhydride racemic
Issue Date:	2008
Publisher:	Elsevier Ltd. www.elsevier.com/ locate/tetlet
Citation:	Chola, J. and Masesane, I.B. (2008) Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl b-amino acid derivatives, Tetrahedron Letters 49, pp. 5680–5682
Abstract:	Stereoselective syntheses of racemic (1S,2R,3R,4R,5S,6R)- and (1S,2R,3R,4S,5S,6R)-3,4,5,6-tetrahydroxy derivatives of 2-aminocyclohexanecarboxylic acid have been achieved by a stereospecific Diels–Alder reaction between furan and maleic anhydride, a Curtius rearrangement and hydroxylation reactions.
URI:	http://hdl.handle.net/10311/325
ISSN:	0040-4039
Appears in Collections:	Research articles (Dept of Chemistry)

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