Photochemical reaction of phenyl-substituted 1, 3-diketones
M Yoshioka, T Suzuki, M Oka
Index: Yoshioka; Suzuki; Oka Bulletin of the Chemical Society of Japan, 1984 , vol. 57, # 6 p. 1604 - 1607
Full Text: HTML
Citation Number: 8
Abstract
Irradiation of 2, 2-dimethyl-1-phenyl-1, 3-diketones with 3-ethyl or 3-isopropyl substituents gave type II cyclization product, 3-hydroxy-2, 2, 4-trimethyl-3-phenylcyclobutanone or 3- hydroxy-2, 2, 4, 4-tetramethyl-3-phenylcyclobutanone, along with type I cleavage products. The type II cyclization/type I cleavage ratio is greater with a 3-isopropyl group than with a 3- ethyl group. A similar irradiation of 2, 2-dimethyl-1-phenyl-1, 3-butanedione gave type I ...
Related Articles:
[Bertrand, M. P.; Oumar-Mahamat, H.; Surzur, J. M. Tetrahedron Letters, 1985 , vol. 26, # 9 p. 1209 - 1212]
[Baker, James; Hedges, Winston; Timberlake, Jack W.; Trefonas, Louis M. Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 855 - 859]
[Ito,Y. et al. Journal of the American Chemical Society, 1975 , vol. 97, p. 2912 - 2914]
[Chassin,C. et al. Journal of the American Chemical Society, 1974 , vol. 96, # 2 p. 606 - 608]
[Baker, James; Hedges, Winston; Timberlake, Jack W.; Trefonas, Louis M. Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 855 - 859]