Photoisomerization reactions can also occur in 4-acylisoxazoles, leading to the conversion of one isomer into another when exposed to light. The exact isomerization mechanism may depend on the specific structure of the 4-acylisoxazole.
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2-methyl-5-phenyl-oxazole-4-carbonyl chloride
3
2-hexadecyloxy-4-nitrotoluene
all-trans-1,6-Diphenyl-1,3,5-hexatriene radical anion
Benzene, 1-(2-phenylethenyl)-3-[2-[2,4,6-tris(1-methylethyl)phenyl]ethenyl]-, (E,E)-
4-{(E)-[4-(dimethylamino)phenyl]diazenyl}benzaldehyde
4-methoxy-2,3,5,6-tetrabromobenzyl bromide
2-deuterio-2-(4-nitrophenyl)-1,3-dithiane
C15H22N3O4P
3-Pentenoic acid, 2,4-dimethyl-, phenylmethyl ester, (R)-
2-
1,2-bis(4-bromo-2-nitrophenyl)ethane
Phenol, 4-methyl-2-(phenylazo)-, (E)-
BENZENE,1,1'-(1,2-ETHENEDIYL)
