When benzosulfone molecules are exposed to UV light, it absorbs energy and undergoes homolytic cleavage, resulting in the formation of two radicals.
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1-(4-fluorophenyl)-1,4-dihydro-2,3-benzoxathiin-3-oxide
3-Eth-(E)-ylidene-4,4-diphenyl-oxetane-2-carboxylic acid ethyl ester
C12H15NO5Se
7(4H)-Benzofuranone, 5,6-dihydro-
2-(1-p-tolylbut-3-enyl)malononitrile
1H-Pyrrole, 2,3-diphenyl-
Carbamic acid, [(3-aminophenyl)methyl]-, 9H-fluoren-9-ylmethyl ester
3-(2-methoxyethoxy)phenol
N-Boc-O-(4-hydroxyphenacyl)-Ala-Ala
C27H35N3O8
octanedioic acid [4-(3-amino-phenyl)-thiazol-2-yl]-amide methyl ester
2',3',5'-tris-O-(tert-butyldimethylsilyl)-N2-cyclopropyl-O6-(mesitylsulfonyl)guanosine
