Issue 5, 1989

Intramolecular nucleophilic addition to photochemically generated ketenes as a versatile route to lactones and lactams; synthesis of a mosquito pheromone, goniothalamin, argentilactone, and the Streptomyces L-factor

Abstract

Photolysis of hydroxy-, dihydroxy- and amino-bicyclo[n.2.0]alkanones has been used as the key step in the synthesis of naturally occurring lactones including a mosquito pheromone, goniothalamin, argentilactone, and the Streptomyces L-factor, and of a γ-lactam.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 303-304

Intramolecular nucleophilic addition to photochemically generated ketenes as a versatile route to lactones and lactams; synthesis of a mosquito pheromone, goniothalamin, argentilactone, and the Streptomyces L-factor

S. S. Rahman, B. J. Wakefield, S. M. Roberts and M. D. Dowle, J. Chem. Soc., Chem. Commun., 1989, 303 DOI: 10.1039/C39890000303

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