Sensitized photo-oxygenation of acyclic conjugated dienes
M Matsumoto, S Dobashi, K Kuroda, K Kondo
Index: Matsumoto, Masakatsu; Dobashi, Satoshi; Kuroda, Keiko; Kondo, Kiyosi Tetrahedron, 1985 , vol. 41, # 11 p. 2147 - 2154
Full Text: HTML
Citation Number: 53
Abstract
Sensitized photo-oxygenation of a wide variety of acyclic 1, 3-dienes was investigated. The 1, 4-cycloaddition of singlet oxygen to acyclic conjugated dienes was closely related to the thermal Diels-Alder reaction in stereospecificity, and steric and electronic effects of substituents. Reactivity order of singlet oxygen toward conjugated dienes and isolated C—C double bonds was exhibited as follows: trisubstituted mono-olefins> 2-substituted 1, 3- ...
Related Articles:
Homogeneous oxidation reactions of propanediols at low temperatures
[ChemSusChem, , vol. 3, # 9 p. 1063 - 1070]
[Journal of Catalysis, , vol. 286, p. 206 - 213]
Oxetene: synthesis and energetics of electrocyclic ring opening
[Journal of the American Chemical Society, , vol. 102, # 16 p. 5429 - 5430]
[Nieuwenhuizen, M.S.; Kieboom, A.P.G.; Bekkum, H. van Recueil: Journal of the Royal Netherlands Chemical Society, 1982 , vol. 101, # 10 p. 339 - 342]
[Bulletin de la Societe Chimique de France, , # 6 p. 745 - 752]