A STUDY OF THE COMPETITION BETWEEN THE DI-PI-METHANE AND THE AZADI-PI-METHANE PROCESSES IN 2-VINYL-BETA,GAMMA-UNSATURATED OXIME DERIVATIVES- THE NOVEL AZADI-PI-METHANE REACTIVITY OF GAMMA-UNSATURATED OXIMES
D. Armesto et al., A STUDY OF THE COMPETITION BETWEEN THE DI-PI-METHANE AND THE AZADI-PI-METHANE PROCESSES IN 2-VINYL-BETA,GAMMA-UNSATURATED OXIME DERIVATIVES- THE NOVEL AZADI-PI-METHANE REACTIVITY OF GAMMA-UNSATURATED OXIMES, Journal of organic chemistry, 59(26), 1994, pp. 8115-8124
A study aimed at detecting intramolecular competition between the di-p
i-methane (DPM) rear-rangement and the azadi-pi-methane (ADPM) process
has been carried out. The results show that direct or acetophenone-se
nsitized irradiation of 2-(2,2-diphenylvinyl)-2-methyl-4,4-diphenyl-3-
butenal oxime acetate 3 and the corresponding oxime trifluoroacetate
11 undergo only the DPM process to yield cyclopropanes. Similar DPM re
arrangement was observed for 2-methyl-4,4-diphenyl-2-vinyl-3-butenonit
rile 22. These are examples of triplet DPM reactivity in acyclic subst
rates where the central carbon has only one electron-withdrawing group
. There is only one case of such reactivity in the aryl di-pi-methane
process. However, 2-methyl-4,4-diphenyl-2-vinyl-2-vinyl-3-butenal oxim
e acetate 26 and the corresponding trifluoroacetate 15 undergo the ADP
M rearrangement exclusively on direct or acetophenone-sensitized irrad
iation. The selectivity observed is interpreted as being dependent on
the relative stabilities of the 1,4-bridged biradical intermediates. B
ased on previous failures to observe the ADPM reactions of beta,gamma-
unsaturated oximes, an attempt to suppress the ADPM reactivity in comp
ounds with a substitution pattern such as that present in 15 and 26 wa
s made using the parent oxime 21. Surprisingly this compound reacts ef
ficiently by the ADPM process and affords cyclopropane 30. This is the
first example of ADPM reactivity of an acyclic beta,gamma-unsaturated
oxime. Ah the rearrangements described are stereoselective. This reac
tion was extended to other oximes 45, 47a and 47b and also to the oxim
e ether 36. The photoreaction of 47b shows that the ADPM rearrangement
of oximes can be extended to ketone derivatives. Previous studies hav
e shown that such reactivity is uncommon. beta,gamma-Unsaturated oxime
s are usually considered to be photochemically inert but these results
have shown that changes in substitution can promote efficient ADPM re
activity.