Journal of the Chemical Society. Chemical communications p. 1483 - 1485 (1989)
Update date:2022-08-18
Topics:
Ashwell, Susan
Davies, Alwyn G.
Golding, Bernard T.
Hay-Motherwell, Robyn
Mwesigye-Kibende, Samson
Photolysis of di-t-butyl 1-bromomethylcyclopropane-1,2-dicarboxylate (1a) in cyclopropane containing triethylsilane and di-t-butyl peroxide gave the 4-methylenepent-2-yl-1,5-dioic acid radical (3c), which was also produced from treatment of (1a), its cis-isomer (2b), di-t-butyl-2-bromo-4-methyleneglutarate (3a), or di-t-butyl 2-bromomethyl-3-methylenesuccinate (4b), with triphenyltin hydride; these experiments support a mechanism via proteinbound free radicals for the B12-dependent enzyme α-methyleneglutarate mutase.
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