The elusive aldol reaction of enolates with aldolates - a highly stereoselective process using three different carbonyl components

Schmittel, Michael and Haeuseler, Andreas and Nilges, Tom and Pfitzner, Arno (2003) The elusive aldol reaction of enolates with aldolates - a highly stereoselective process using three different carbonyl components. CHEMICAL COMMUNICATIONS (1). pp. 34-35. ISSN 1359-7345

Full text not available from this repository. (Request a copy)

Abstract

Three different carbonyl components are assembled to tetrahydropyran-2,4-diols by two successive diastereoselective aldol reactions.

Item Type: Article
Uncontrolled Keywords: TISHCHENKO REACTIONS; CLAISEN CONDENSATION; CONJUGATE ADDITION; SEQUENCE; AGENT;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Arbeitskreis Prof. Dr. Robert Wolf
Depositing User: Dr. Gernot Deinzer
Date Deposited: 25 Aug 2021 10:53
Last Modified: 25 Aug 2021 10:53
URI: https://pred.uni-regensburg.de/id/eprint/39410

Actions (login required)

View Item View Item