Issue 2, 2003
From the journal:

Chemical Communications

A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using an hetero Diels–Alder/allylboration sequence

Michael Deligny,a   François Carreaux,*a   Bertrand Carboni,a   Loïc Toupetb  and  Gilles Dujardinc  

* Corresponding authors

a Synthèse et Electrosynthèse organiques, Institut de Chimie, UMR 6510 CNRS, Campus de Beaulieu, 35042 Rennes Cedex, France
E-mail: francois.carreaux@univ-rennes1.fr

b GMCM, CNRS, Université de Rennes 1, 35042 Rennes Cedex, France

c Laboratoire de Synthèse Organique, UMR 6011 CNRS, Université du Maine, 72085 Le Mans Cedex, France

Abstract

The development of a new strategy for the synthesis of α-hydroxyalkyl dihydropyrans is reported. This approach is based on a tandem hetero[4 + 2]/allylboration reaction.

Graphical abstract: A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using an hetero Diels–Alder/allylboration sequence

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Article information

DOI
https://doi.org/10.1039/B208572K
Article type
Communication
Submitted
25 Sep 2003
Accepted
03 Oct 2003
First published
14 Nov 2003

Chem. Commun., 2003, 276-277

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A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using an hetero Diels–Alder/allylboration sequence

M. Deligny, F. Carreaux, B. Carboni, L. Toupet and G. Dujardin, Chem. Commun., 2003, 276 DOI: 10.1039/B208572K

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