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2000
Volume 4, Issue 2
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

Thio-Claisen rearrangement of symmetrically substituted 1,4-but-2-ynes (3a,b and 4) exhibit tandem cyclization and afforded compounds 5a,b and 6 in good yields. These sulphides 3a,b and 4 were in turn prepared from commercially available thiophene. The key step in this transformation is tandem [3,3] sigmatropic rearrangement.

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/content/journals/loc/10.2174/157017807780414091
2007-03-01
2025-10-04
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