Mc. Jimenez et al., Di-pi-methane photorearrangement of trans-1,3-diphenylpropene upon excitation to higher singlet states in polar solvents, CHEM COMMUN, (23), 2000, pp. 2341-2342
A dramatic enhancement of the di-pi -methane rearrangement is observed upon
excitation of trans-1,3-diphenylpropene (1) to its higher singlet states i
n acetonitrile, which leads to trans-1,2-diphenylcyclopropane (3) as a majo
r photoproduct.