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2002•Chemical CommunicationsRequires access

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

Michael Schmittel, Andreas Haeuseler, Tom Nilges, Arno Pfitzner

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Abstract

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

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What this paper is about

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

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OpenAlex reports 5 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

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

Key concepts: Aldol reaction, Tetrahydropyran, Stereoselectivity, Chemistry, Organic chemistry, Combinatorial chemistry, Catalysis, Ring (chemistry)

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