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dc.contributor.authorM.S.NEDJIMI, and Lakhdar SEKHRI-
dc.date.accessioned2013-12-19T15:00:19Z-
dc.date.available2013-12-19T15:00:19Z-
dc.date.issued2013-12-19-
dc.identifier.issnsaf-
dc.identifier.urihttp://hdl.handle.net/123456789/2815-
dc.description1st International Days of Organometallic Chemistry and Catalysis JICOC Ouargla, February 06- 09, 2012en_US
dc.description.abstractA range of prochiral acetophenone derivatives have been converted efficiently to the corresponding (R)- alcohols with > 80% yield and good enantioselectivities (up to 70% ee). Cyclic ketones are also reduced with high levels of stereoselectivity with PMHS in the presence of TBAF and baker's yeast, in particular 4-methylcyclohaxanone (trans: cis 84:16). High stereoselectivity is also observed in the reduction of 2-cyanobenzaldehyde and anti- imine was obtained in 71%.en_US
dc.language.isoenen_US
dc.relation.ispartofseries2012;-
dc.subjectasymmetric reductionen_US
dc.subjectbiocatalysten_US
dc.subjectbacker's yeasten_US
dc.subjectTBAFen_US
dc.subjectPMHSen_US
dc.titleThe asymmetric reduction of prochiral ketones using tetrabutylammonium fluoride, polymethylhydrosiloxane and biocatalysts, baker's yeasten_US
dc.typeArticleen_US
Appears in Collections:1. Faculté des mathématiques et des sciences de la matière

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