Effect of a Strategically Positioned Methoxy Substituent on the Photochemistry of 3-Aryl-3H-1-Oxacyclopenta[l]Phenanthren-2-Ones

摘要

Irradiation of 3-methoxy-3-aryl-3H-1-oxacyclopenta[l]phenanthren-2-one derivatives5a–dresulted in singlet-mediated decarbonylation reaction leading to the formation of phenanthrene derivatives9a–d. The structure of the photoproduct was unequivocally established on the basis of X-ray crystallographic analysis.