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2000
Volume 3, Issue 7
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A direct synthesis of substituted oxepin and spiroheterocycles has been achieved from substrates derived from 4-hydroxy-1,6-dimethyl pyridine-2-ones (1) by combining Claisen rearrangement and ring closing enyne metathesis. The RCEM proceeded smoothly under nitrogen atmosphere at room temperature in the presence of well-defined ruthenium catalyst A (10 mol%).

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/content/journals/loc/10.2174/157017806778341816
2006-07-01
2025-10-03
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/content/journals/loc/10.2174/157017806778341816
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  • Article Type:
    Research Article
Keyword(s): 2-Pyridone; Claisen rearrangement; enyne metathesis; oxepin; ring-closing metathesis
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