Issue 6, 2000

Lewis acid-catalysed sequential reaction in ionic liquids

Abstract

The utility of ionic liquids as a safe recyclable reaction media at 200 °C in the presence of anhydrous scandium trifluoromethanesulfonate for a sequential reaction involving a Claisen rearrangement and cyclizations is discribed.

Article information

Article type
Paper
Submitted
15 Aug 2000
First published
06 Nov 2000

Green Chem., 2000,2, 296-297

Lewis acid-catalysed sequential reaction in ionic liquids

F. Zulfiqar and T. Kitazume, Green Chem., 2000, 2, 296 DOI: 10.1039/B006684M

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