Issue 1, 2004
From the journal:

Chemical Communications

Directed regio- and stereoselective hydroformylation of mono- and 1,3-disubstituted allylic alcohols: a catalytic approach to the anti-aldol-retron†

Bernhard Breit,*a   Peter Demela  and  Antje Geberta  

* Corresponding authors

a Institut für Organische Chemie und Biochemie, Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104 Freiburg, Germany
E-mail: bernhard.breit@organik.chemie.uni-freiburg.de
Fax: 0049-761-2038715
Tel: 0049-761-2036051

Abstract

Regioselective and diastereoselective hydroformylation of mono- and 1,3-disubstituted allylic alcohol o-DPPB esters is described. The products represent synthetically important anti-aldol retrons.

Graphical abstract: Directed regio- and stereoselective hydroformylation of mono- and 1,3-disubstituted allylic alcohols: a catalytic approach to the anti-aldol-retron

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Article information

DOI
https://doi.org/10.1039/B311378G
Article type
Communication
Submitted
18 Sep 2003
Accepted
24 Oct 2003
First published
11 Nov 2003

Chem. Commun., 2004, 114-115

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Directed regio- and stereoselective hydroformylation of mono- and 1,3-disubstituted allylic alcohols: a catalytic approach to the anti-aldol-retron

B. Breit, P. Demel and A. Gebert, Chem. Commun., 2004, 114 DOI: 10.1039/B311378G

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