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Metathetic approach to naphthoxepin and spirocyclic molecular frameworks

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
45
Issue
7
Identifiers
DOI: 10.1016/j.tetlet.2003.12.075
Keywords
  • Claisen Rearrangement
  • Metathesis
  • Oxepins
  • Spiro Compounds

Abstract

Abstract An efficient method for the synthesis of naphthoxepin and spirocyclic skeletons starting from β-naphthol has been developed. The Claisen rearrangement and the ring-closing metathesis reaction are used as key steps for their assembly.

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