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

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

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

Original language	English
Pages (from-to)	34-35
Number of pages	2
Journal	Chemical Communications
Issue number	1
DOIs	https://doi.org/10.1039/b209536j
State	Published - 2003
Externally published	Yes

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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",

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language = "English",

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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.

AB - 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

M3 - Article

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SN - 1359-7345

SP - 34

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JO - Chemical Communications

JF - Chemical Communications

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ER -

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

Abstract

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