An enantioselective synthesis of β2-amino acid derivatives

Elaridi, Jomana; Thaqi, Ali; Prosser, Andrew; Jackson, W. Roy; Robinson, Andrea J.

dc.contributor.author	Elaridi, Jomana
dc.contributor.author	Thaqi, Ali
dc.contributor.author	Prosser, Andrew
dc.contributor.author	Jackson, W. Roy
dc.contributor.author	Robinson, Andrea J.
dc.date.accessioned	2015-12-22T09:03:39Z
dc.date.available	2015-12-22T09:03:39Z
dc.date.copyright	2005
dc.date.issued	2015-12-22
dc.identifier.issn	1362-511X	en_US
dc.identifier.uri	http://hdl.handle.net/10725/2867
dc.description.abstract	Enantioselective hydrogenation of a series of (E)-α-substituted β-amidoacrylates using Rh(I)-catalysts with chiral phosphine ligands (BPE, DuPHOS) gives β2-amino acid derivatives with enantioselectivities of up to 67%. A β2,3-amino acid derivative was also synthesised with similar enantioselectivity (⩽65%) from the corresponding prochiral enamide.	en_US
dc.language.iso	en	en_US
dc.title	An enantioselective synthesis of β2-amino acid derivatives	en_US
dc.type	Article	en_US
dc.description.version	Published	en_US
dc.author.school	SAS	en_US
dc.author.idnumber	201100947	en_US
dc.author.woa	N/A	en_US
dc.author.department	Natural Sciences	en_US
dc.description.embargo	N/A	en_US
dc.relation.journal	Tetrahedron: Asymmetry	en_US
dc.journal.volume	16	en_US
dc.journal.issue	7	en_US
dc.article.pages	1309-1319	en_US
dc.identifier.doi	http://dx.doi.org/10.1016/j.tetasy.2005.01.048
dc.identifier.ctation	Elaridi, J., Thaqi, A., Prosser, A., Jackson, W. R., & Robinson, A. J. (2005). An enantioselective synthesis of β< sup> 2</sup>-amino acid derivatives. Tetrahedron: Asymmetry, 16(7), 1309-1319.	en_US
dc.author.email	jomana.aridi@lau.edu.lb
dc.identifier.url	http://www.sciencedirect.com/science/article/pii/S0957416605001473