5820-02-0Relevant articles and documents
Novel photochemical behaviour of the oximes and hydrazones of β,γ-unsaturated carbonyl compounds
Armesto, Diego,Ramos, Ana,Ortiz, Maria J.,Horspool, William M.,Mancheno, Maria J.,Caballero, Olga,Mayoral, Elena P.
, p. 1535 - 1541 (2007/10/03)
A study of the photochemical reactivity of a series of β,γ-unsaturated oximes and hydrazone derivatives under triplet sensitized conditions has been carried out. The oximes 3c, 4a and 4c cyclize to the corresponding dihydroisoxazoles 5c, 6a and 6c while t
Substitution Effects on the Aza-di-?-methane Rearrangement of Imines
Armesto, Diego,Horspool, William M.,Langa, Fernando,Perez-Ossorio, Rafael
, p. 1039 - 1042 (2007/10/02)
The u.v. irradiation of several 1-aryl derivatives of 3,3-dimethyl-5,5-diphenyl-1-azapenta-1,4-diene has been carried out.All of them undergo the aza-di-?-methane rearrangement and yield a cyclopropylimine.The influence of substituents on the 1-aryl group has given support for the proposal that imines with a low ionization potential are less efficient at undergoing the aza-di-?-methane process than imines with a higher ionization potential.This was demonstrated in a quantitative fashion.The involvement of an electron-transfer process in the reaction is discussed.
A NOVEL AZA-DI-?-METHANE REARRANGEMENT THE PHOTOREACTION OF 4,4-DIMETHYL-1,6,6-TRIPHENYL-2-AZA-HEXA-2,5-DIENE
Armesto, Diego,Martin, Juan Antonio F.,Perez-Ossorio, Rafael
, p. 2149 - 2152 (2007/10/02)
The synthesis and the novel photochemical aza-di-?-methane reaction of 4,4-dimethyl-1,6,6-triphenyl-2-aza-hexa-2,5-diene are described.