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

doi:10.1039/b209536j

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

Publikation: Beitrag in Fachzeitschrift › Artikel › Begutachtung

5 Zitate (Scopus)

Abstract

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

Originalsprache	Englisch
Seiten (von - bis)	34-35
Seitenumfang	2
Fachzeitschrift	Chemical Communications
Ausgabenummer	1
DOIs	https://doi.org/10.1039/b209536j
Publikationsstatus	Veröffentlicht - 2003
Extern publiziert	Ja

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10.1039/b209536j

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title = "The elusive aldol reaction of enolates with aldolates - A highly stereoselective process using three different carbonyl components",

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

author = "Michael Schmittel and Andreas Haeuseler and Tom Nilges and Arno Pfitzner",

year = "2003",

doi = "10.1039/b209536j",

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journal = "Chemical Communications",

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AU - Schmittel, Michael

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AU - Nilges, Tom

AU - Pfitzner, Arno

PY - 2003

Y1 - 2003

N2 - Three different carbonyl components are assembled to tetrahydropyran-2,4-diols by two successive diastereoselective aldol reactions.

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DO - 10.1039/b209536j

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SN - 1359-7345

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JO - Chemical Communications

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

Abstract

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