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Synthesis 2004(3): 389-400
DOI: 10.1055/s-2004-815915
DOI: 10.1055/s-2004-815915
PAPER
© Georg Thieme Verlag Stuttgart · New York
Epoxide Formation by Indirect Electroreductive Coupling between Aldehydes or Ketones and Activated gem-Dichloro Compounds
Further Information
Received
5 November 2003
Publication Date:
13 January 2004 (online)
Publication History
Publication Date:
13 January 2004 (online)
Abstract
Epoxides are prepared by indirect electroreductive coupling of carbonyl compounds (aldehydes or ketones) and activated gem-dichloro compounds. This process is more efficient with aryl ketones than with aryl aldehydes. Though yields are only moderate, this method offers the valuable advantage of avoiding the use of strong bases or peroxides.
Key words
epoxides - coupling - aldehydes - ketones - condensation - reductions
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