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Diastereomeric Oxathia[n](1,1′)ferrocenophanes
Authors:Bronis?aw Czech  Aleksander Ratajczak  Krzysztof Nagraba
Institution:(1) Department of Organic Synthesis, Silesian University, 40006 Katowice, Poland;(2) Regional Laboratory of Physicochemical Analysis and Structural Research, Jagiellonian University, 30060 Cracow, Poland
Abstract:Zusammenfassung Neue Oxathiaferrocenophane wurden durch Umsetzung von 1,1prime-Bis(hydroxymethyl)ferrocen mit Dithiolen dargestellt, welche Sauerstoff in den Alkylketten enthalten. Die Reaktion von 1,1prime-Bis(agr-hydroxyethyl)ferrocenen mit Dithiolen führte zu Mischungen von Diastereomeren, aus welchen reine Stereoisomere isoliert und charakterisiert wurden. Einige Aspekte des stereochemischen Verlaufes dieser Reaktionen werden diskutiert.
Diastereomere oxathian](1,1prime)ferrocenophane
Novel oxathiaferrocenophanes have been synthesized by the reaction of 1,1prime-bis(hydroxymethyl)ferrocene with dithiols bearing oxygen in chains. The reactions of 1,1prime-bis(agr-hydroxyethyl)ferrocenes with dithiols afforded mixtures of diastereomeric products from which pure stereoisomers were isolated and characterized. Some aspects concerning a stereochemical course of the reactions described are discussed.
Keywords:1  1prime-Bis(gif" alt="prime" align="BASELINE" BORDER="0">-Bis(agr-hydroxyalkyl)ferrocenes" target="_blank">gif" alt="agr" align="BASELINE" BORDER="0">-hydroxyalkyl)ferrocenes  reactions with dithiols  Diastereomers  Ferrocene polyoxathiaethers  Oxathiaferrocenophanes
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