SYNTHESIS OF CHIRALS REGIOISOMERS FROM D-MANNITOL: OBTAINMENT OF A ACETYLENIC ALCOHOLS MIXTURE.

dc.creatorCito, AMDL
dc.creatorAraujo, BQ
dc.creatorLopes, JAD
dc.creatorMagalhaes, AF
dc.creatorMagalhaes, EG
dc.date2009
dc.date2014-11-15T16:33:21Z
dc.date2015-11-26T16:12:25Z
dc.date2014-11-15T16:33:21Z
dc.date2015-11-26T16:12:25Z
dc.date.accessioned2018-03-28T23:00:40Z
dc.date.available2018-03-28T23:00:40Z
dc.identifierQuimica Nova. Soc Brasileira Quimica, v. 32, n. 9, n. 2355, n. 2359, 2009.
dc.identifier0100-4042
dc.identifierWOS:000273059500023
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/79231
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/79231
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/79231
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1267265
dc.descriptionSYNTHESIS OF CHIRALS REGIOISOMERS FROM D-MANNITOL: OBTAINMENT OF A ACETYLENIC ALCOHOLS MIXTURE. The synthesis of chiral acetylenic regioisomers was described by using an appropriate intermediate such as isopropylidene glycerol, a synthon widely used in the enantioselective syntheses. This intermediate was prepared from D-mannitol. The nine obtained compounds have been characterized by their respective spectral data. The mixture of chiral acetylenic alcohols showed activity against Escherichia coli when tested through the monitoring of CO(2) released during microbial respiration by using a conductimetric system.
dc.description32
dc.description9
dc.description2355
dc.description2359
dc.languagept
dc.publisherSoc Brasileira Quimica
dc.publisherSao Paulo
dc.publisherBrasil
dc.relationQuimica Nova
dc.relationQuim. Nova
dc.rightsaberto
dc.sourceWeb of Science
dc.subjectD-mannitol
dc.subjectacetylenic alcohols
dc.subjectE. coli
dc.subjectEscherichia-coli
dc.subjectMarine Sponge
dc.subjectEfficient
dc.titleSYNTHESIS OF CHIRALS REGIOISOMERS FROM D-MANNITOL: OBTAINMENT OF A ACETYLENIC ALCOHOLS MIXTURE.
dc.typeArtículos de revistas


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