Photochemical generation of aliphatic radicals from benzophenone oxime esters: simple synthesis of alkylbenzenes and alkylpyridines
M Hasebe, T Tsuchiya
Index: Hasebe, Masato; Tsuchiya, Takashi Tetrahedron Letters, 1986 , vol. 27, # 28 p. 3239 - 3242
Full Text: HTML
Citation Number: 29
Abstract
Abstract Photolysis of benzophenone oxime esters, prepared with aliphatic carboxylic acids and benzophenone oxime, in benzene and pyridine generates various primary, secondary and tertiary aliphatic radicals selectively, and corresponding alkylbenzenes and alkylpyridines are produced in good yields, respectively.
Related Articles:
Nickel catalyzed electrochemical heteroarylation of activated olefins
[Condon, Sylvie; Dupre, Daniel; Lachaise, Isabelle; Nedelec, Jean-Yves Synthesis, 2002 , # 12 p. 1752 - 1758]
Reaction of 1-pyridyl-1, 3-butanediones and 1, 3-dipyridyl-1, 3-propanediones
[Ferles, Miloslav; Kafka, Stanislav; Silhankova, Alexandra; Sputova, Michaela Collection of Czechoslovak Chemical Communications, 1981 , vol. 46, # 5 p. 1167 - 1172]