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The reactivity of intradiol-cleaving catechol dioxygenases can be modeled with the complex cation 1. The complex reacts nearly quantitatively with molecular oxygen yielding 3,5-di-tert-butylmuconic anhydride (3) and 3,5-di-tert-butyl-5-carboxymethyl-2-furanone in a 1:1 ratio. The catalytic oxygenation reaction of 2 [Eq. (a)] gives 3 in 70% yield and with a turnover number of 54. dbcH2 = 3,5-di-tert-butylcatechol; L-N4Me2 = N,N′-dimethyl-2,11-diaza[3.3](2,6)pyridinophane.
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Koch et al. (1996) studied this question.
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