Asymmetric synthesis of glutamate derivatives

dc.contributor.author	Seck, Rokhyatou
dc.contributor.author	Gassama, Abdoulaye
dc.contributor.author	Nour, Mohammed
dc.contributor.author	Demange, Luc
dc.contributor.author	Cavé, Christian
dc.date.accessioned	2023-03-03T13:05:46Z
dc.date.available	2023-03-03T13:05:46Z
dc.date.issued	2017
dc.identifier.uri	http://rivieresdusud.uasz.sn/xmlui/handle/123456789/1720
dc.description.abstract	Analogs of glutamic acid were synthesized through the asymmetric Michael reaction using chiral acyclic E-enaminoesters and various Michael acceptors. The influence of the alkoxy group of the enaminoesters and also the nature of the olefins in the presence or not of zinc chloride on yield and enantioselectivity are explored.	en_US
dc.language.iso	en	en_US
dc.relation.ispartofseries	Arkivoc;2017, part iv : pp.51-62
dc.subject	Glutamic acid	en_US
dc.subject	Michael addition	en_US
dc.subject	Symmetric synthesis	en_US
dc.subject	β-enaminoesters	en_US
dc.subject	Zinc chloride	en_US
dc.title	Asymmetric synthesis of glutamate derivatives	en_US
dc.type	Article	en_US
dc.territoire	Région de Ziguinchor	en_US