Enantioselective Photochemical Reactions of 2-Pyridones in Solution

Two key photochemical reactions of prochiral 2-pyridones were studied in the presence of a chiral host. The [4 + 4]-photocycloaddition with
cyclopentadiene (CpH) proceeded smoothly and with high enantioselectivity (84−87% ee). The absolute configuration of the endo-diastereoisomer
was established by X-ray crystallography. The electrocyclic [4π]-ring closure to 3-oxo-2-azabicyclo[2.2.0]-5-hexenes occurred with lower
enantioselectivity (20−23% ee at −20 °C). The velocity of the latter reaction slowed significantly with decreasing temperature.