STEREOCHEMICAL ANALYSIS IN 22-MEMBERED MACROLIDES BASED ON MOLECULAR MODELING.

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DC Field	Value	Language
dc.contributor.author	S. BELAIDI	-
dc.contributor.author	A. DIBI	-
dc.contributor.author	M. OMARI	-
dc.contributor.author	T. LANEZ	-
dc.date.accessioned	2006	-
dc.date.available	2006	-
dc.date.issued	2006	-
dc.identifier.issn	2170-0672	-
dc.identifier.uri	http://dspace.univ-ouargla.dz/jspui/handle/123456789/6491	-
dc.description	AST Annales des Sciences et Technologie	en_US
dc.description.abstract	Conformational analysis of macrolides with 22-ring membered has been carried out using molecular modeling (molecular mechanics and molecular dynamics). The results indicate that each investigated macrocycles present eight types of preferential conformations. They result of the combination of two systems diene and ester a,b-unsaturated. A high conformational mobility of no complexed macrocycles (22) was obtained. In presence of tricarbonyliron, the number of the privileged conformations was reduced.	en_US
dc.language.iso	fr	en_US
dc.relation.ispartofseries	volume 1 numéro 1 AST 2006;	-
dc.subject	STEREOCHEMICAL ANALYSIS	en_US
dc.title	STEREOCHEMICAL ANALYSIS IN 22-MEMBERED MACROLIDES BASED ON MOLECULAR MODELING.	en_US
dc.type	Article	en_US
Appears in Collections:	volume 1 numéro 1 AST 2006

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