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dc.contributor.authorLewkowski, Jarosław
dc.contributor.authorDzięgielewski, Marek
dc.contributor.authorSzcześniak, Aleksandra
dc.contributor.authorCiechańska, Magdalena
dc.date.accessioned2014-08-27T07:14:52Z
dc.date.available2014-08-27T07:14:52Z
dc.date.issued2011-11
dc.identifier.issn2028 - 3997
dc.identifier.urihttp://hdl.handle.net/11089/5342
dc.description.abstractA series of 2,5-Furanyl-bis-(aminomethylphosphonic Acids) has been synthesized by the addition of di(trimethylsilyl) phosphite to azomethine bond of achiral Schiff bases derved from 2,5-diformylfuran. The stereochemical aspect of this reaction has been studied and compared with the behaviour of achiral terephthalic Schiff bases in similar reaction. Whereas, addition to achiral terephthalic Schiff bases was found to be highly stereoselective, the analogous reaction with achiral 2,5-diformylfuran Schiff bases was stereoselective exclusively in the case when the substituent is benzyl.pl_PL
dc.description.sponsorshipN/Apl_PL
dc.language.isoenpl_PL
dc.publisherMedJChempl_PL
dc.relation.ispartofseriesMediterranean Journal of Chemistry;2011, 1(3)
dc.subject2,5-diformylfuran Schiff basespl_PL
dc.subjectdi(trimethylsilyl) phosphitepl_PL
dc.subjectadditionpl_PL
dc.subjectazomethine bondpl_PL
dc.titleAddition of Di(trimethylsilyl) Phosphite to Schiff Bases of 2,5-Diformylfuranpl_PL
dc.typeArticlepl_PL
dc.page.number135-144pl_PL
dc.contributor.authorAffiliationDept of Organic Chemistry, Faculty of Chemistry, University of Łódź, Tamka 12, 91-403 Łódź, POLANDpl_PL


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