TOTAL SYNTHESIS OF ALKALOIDS OF GALIPEA OFFICINALIS

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DC Field	Value	Language
dc.contributor.author	F. Louafi, J.-P. Hurvois	-
dc.contributor.author	S. Shahane, J. Moreau	-
dc.contributor.author	A.Chibani	-
dc.date.accessioned	2016-11-16T09:22:02Z	-
dc.date.available	2016-11-16T09:22:02Z	-
dc.date.issued	2016-11-16	-
dc.identifier.uri	http://dspace.univ-ouargla.dz/jspui/handle/123456789/12347	-
dc.description	Le 2ème Séminaire International sur les Plantes Médicinales SIPM'2	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.subject	Alkaloids	en_US
dc.subject	Galipea Officinalis	en_US
dc.subject	umpolung	en_US
dc.subject	tetrahydroquinoline	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

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