Issue 14, 2003

3-Chloropropenyl pivaloate in organic synthesis: the first asymmetric catalytic entry to syn-alk-1-ene-3,4-diols

Abstract

The first asymmetric catalytic synthesis of syn-alk-1-ene-3,4-diols was developed; the regio-, diastereo- and enantioselective addition of 3-chloropropenyl pivaloate to aldehydes was made possible by exploiting Salen–Cr(II) species, in a catalytic version of the Nozaki–Hiyama–Kishi reaction.

Graphical abstract: 3-Chloropropenyl pivaloate in organic synthesis: the first asymmetric catalytic entry to syn-alk-1-ene-3,4-diols

Article information

Article type
Communication
Submitted
25 Apr 2003
Accepted
04 Jun 2003
First published
18 Jun 2003

Chem. Commun., 2003, 1762-1763

3-Chloropropenyl pivaloate in organic synthesis: the first asymmetric catalytic entry to syn-alk-1-ene-3,4-diols

M. Lombardo, S. Licciulli, S. Morganti and C. Trombini, Chem. Commun., 2003, 1762 DOI: 10.1039/B304485H

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