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The elusive aldol reaction of enolates with aldolates--a highly stereoselective process using three different
Michael Schmittel1, Andreas Haeuseler, Tom Nilges
1FB 8-OC1 (Chemie-Biologie), Universität Siegen, Adolf-Reichwein-Str, D-57068 Siegen, Germany. schmittel@chemie.uni-siegen.de
Chemical Communications (Cambridge, England)
|March 4, 2003
Abstract:
Three different carbonyl components are assembled to tetrahydropyran-2,4-diols by two successive diastereoselective aldol reactions.