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

University of Siegen
University of Regensburg

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",

year = "2003",

doi = "10.1039/b209536j",

language = "English",

pages = "34--35",

journal = "Chemical Communications",

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publisher = "Royal Society of Chemistry",

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T1 - The elusive aldol reaction of enolates with aldolates - A highly stereoselective process using three different carbonyl components

AU - Schmittel, Michael

AU - Haeuseler, Andreas

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.

UR - https://www.scopus.com/pages/publications/0037221909

U2 - 10.1039/b209536j

DO - 10.1039/b209536j

M3 - Article

C2 - 12610952

AN - SCOPUS:0037221909

SN - 1359-7345

SP - 34

EP - 35

JO - Chemical Communications

JF - Chemical Communications

IS - 1

ER -

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

Abstract

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