TOTAL SYNTHESIS OF ALKALOIDS OF GALIPEA OFFICINALIS

Please use this identifier to cite or link to this item: https://dspace.univ-ouargla.dz/jspui/handle/123456789/3671

Full metadata record

DC Field	Value	Language
dc.contributor.author	F. Louafi, a J.-P. Hurvois,b S. Shahane,b J. Moreau,b A.Chibani	-
dc.date.accessioned	2013-12-22T11:19:05Z	-
dc.date.available	2013-12-22T11:19:05Z	-
dc.date.issued	2013-12-22	-
dc.identifier.issn	nadjet	-
dc.identifier.uri	http://hdl.handle.net/123456789/3671	-
dc.description	Le 2ème Séminaire International sur les Plantes Médicinales SIPM'2 du 19 au 20 Avril 2011	en_US
dc.description.abstract	In this communication a new and reliable route to Galipea officinalis alkaloids from tetrahydroquinoline has been developed. In this process, the α-CH bond of the tetrahydroquinoline nucleus was activated electrochemically to produce an α-amino nitrile which was condensed with a range of alkyl iodides.	en_US
dc.language.iso	en	en_US
dc.relation.ispartofseries	2011;	-
dc.subject	Alkaloids	en_US
dc.subject	Galipea Officinalis	en_US
dc.subject	umpolung	en_US
dc.title	TOTAL SYNTHESIS OF ALKALOIDS OF GALIPEA OFFICINALIS	en_US
dc.type	Article	en_US
Appears in Collections:	3. Faculté des sciences appliquées

Files in This Item:

File	Description	Size	Format
F. Louafi.pdf		90,86 kB	Adobe PDF	View/Open

DSpace JSPUI