A catalytic asymmetric synthesis of 5,5-dimethylproline

Elaridi, Jomana; Jackson, W. Roy; Robinson, Andrea J.

dc.contributor.author	Elaridi, Jomana
dc.contributor.author	Jackson, W. Roy
dc.contributor.author	Robinson, Andrea J.
dc.date.accessioned	2015-12-22T09:32:28Z
dc.date.available	2015-12-22T09:32:28Z
dc.date.copyright	2005
dc.date.issued	2015-12-22
dc.identifier.issn	1362-511X	en_US
dc.identifier.uri	http://hdl.handle.net/10725/2869
dc.description.abstract	The methyl ester derivative of commercially available N-acetyl-allylglycine readily undergoes cross-metathesis with 2-methylbut-2-ene and ruthenium–alkylidene catalyst to afford the prenylglycine derivative. Acid-catalysed cyclisation then affords 5,5-dimethylproline in near quantitative yield and enantioselectivity.	en_US
dc.language.iso	en	en_US
dc.title	A catalytic asymmetric synthesis of 5,5-dimethylproline	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	11	en_US
dc.journal.issue	6	en_US
dc.article.pages	2025-2029	en_US
dc.identifier.doi	http://dx.doi.org/10.1016/j.tetasy.2005.05.003
dc.identifier.ctation	Elaridi, J., Jackson, W. R., & Robinson, A. J. (2005). A catalytic asymmetric synthesis of 5, 5-dimethylproline. Tetrahedron: Asymmetry, 16(11), 2025-2029.	en_US
dc.author.email	jomana.aridi@lau.edu.lb
dc.identifier.url	http://www.sciencedirect.com/science/article/pii/S0957416605003411