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

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DC Field	Value	Language
dc.contributor.author	Chola, J.
dc.contributor.author	Masesane, I.B.
dc.date.accessioned	2009-06-09T09:50:31Z
dc.date.available	2009-06-09T09:50:31Z
dc.date.issued	2008
dc.identifier.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	en_US
dc.identifier.issn	0040-4039
dc.identifier.uri	http://hdl.handle.net/10311/325
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier Ltd. www.elsevier.com/ locate/tetlet	en_US
dc.subject	tetrahydroxy derivatives	en_US
dc.subject	Stereoselective syntheses	en_US
dc.subject	furan	en_US
dc.subject	maleic anhydride	en_US
dc.subject	racemic	en_US
dc.title	Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl b-amino acid derivatives	en_US
dc.type	Published Article	en_US
Appears in Collections:	Research articles (Dept of Chemistry)

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