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2000
Volume 8, Issue 4
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

Beckmann rearrangement of a variety of ketoximes has been carried out in imidazolium-based ionic liquids in the presence of catalytic amount of stannous chloride. This mild and ‘green’ procedure is highly regioselective affording the corresponding N-substituted amides in good to quantitative yields.

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/content/journals/loc/10.2174/157017811795371403
2011-05-01
2025-09-12
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