Synthesis of naphtho[1,8-bc]pyran derivatives and related compounds through hydroxy group directed C-H bond cleavage under rhodium catalysis

Chem Asian J. 2010 Apr 1;5(4):847-51. doi: 10.1002/asia.200900639.

Abstract

The straightforward and efficient synthesis of naphtho[1,8-bc]pyran derivatives and related polycyclic compounds is achieved by the rhodium-catalyzed oxidative coupling of 1-naphthols or other phenolic and alcoholic substrates with alkynes. In these annulation reactions, the hydroxy groups effectively act as the key function for the regioselective C-H bond cleavage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry
  • Carbon / chemistry
  • Catalysis
  • Naphthols / chemistry*
  • Oxidation-Reduction
  • Pyrans / chemical synthesis
  • Pyrans / chemistry*
  • Rhodium / chemistry*
  • Stereoisomerism

Substances

  • Alkynes
  • Naphthols
  • Pyrans
  • Carbon
  • Rhodium