R. Srinivasan, Lloyd S. White
JACS
Anisole undergoes photochemical 1, 3-addition to a variety of olefins with about the quantum efficiency of benzene but in considerably greater chemical yield. The latter feature may resuit from the stability of the adducts to continued irradiation. A 1, 3 photoadduct of an aromatic compound (anisole) to cyclohexene has been isolated for the first time. All of the 1, 3 adducts rearrange readily on treatment with acid to derivatives of bicyclo[3.2.1]oct-2-en-8-one. © 1977, American Chemical Society. All rights reserved.
R. Srinivasan, Lloyd S. White
JACS
R. Srinivasan, V.B. Jipson, et al.
Surface Science
M. Scheuermann, C.C. Chi, et al.
Applied Physics Letters
E. Sutcliffe, R. Srinivasan
Journal of Applied Physics