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Fert-Butylcatechol

Figure 5.11 Proposed mechanism for the oxidation of 3,5-di-fert-butylcatechol by [Cu2([22]py4pz) ( 4-0H)](Cl04)3H20. The peroxido-dicopper(ll) intermediate was characterized by UV-Vis and resonance Raman spectroscopy [47]. Figure 5.11 Proposed mechanism for the oxidation of 3,5-di-fert-butylcatechol by [Cu2([22]py4pz) ( 4-0H)](Cl04)3H20. The peroxido-dicopper(ll) intermediate was characterized by UV-Vis and resonance Raman spectroscopy [47].
Benzyl alcohol (8) Benzenemethanol (9) (100-51-6) 4-fert-Butylcatechol Pyrocatechol, 4-tert-butyl- (8) 1,2-... [Pg.9]

DTBCH2, 3,5-di-fert-butylcatechol H2ASC, ascorbic acid H2Phen, dihydrophenazine H2FI, dihydrolumiflavin. [Pg.176]

Table 4. Specification and Analysis of 1,3-Butadiene Inhibited with p-fert-butylcatechol (ASTM D1157)... Table 4. Specification and Analysis of 1,3-Butadiene Inhibited with p-fert-butylcatechol (ASTM D1157)...
Despite a typical substrate in the enzymatic system, protocatechuic acid was found to be oxygenated by model complexes not in organic solvents but in water. The highly selective and catalytic intradiol oxygenation of 4-fm-butylcatechol indicated that various types of catechols other than 3,5-di-fert-butylcatechol can be used as substrates in the model systems and that oxygenations by nonheme iron systems in water are attractive. The reactivity and selectivity are dependent on the substituent on catechols and pH of the solution. [Pg.169]

See other pages where Fert-Butylcatechol is mentioned: [Pg.85]    [Pg.575]    [Pg.620]    [Pg.686]    [Pg.118]    [Pg.1095]    [Pg.1225]    [Pg.76]    [Pg.192]    [Pg.164]    [Pg.170]    [Pg.201]    [Pg.85]    [Pg.575]    [Pg.620]    [Pg.686]    [Pg.118]    [Pg.1095]    [Pg.1225]    [Pg.76]    [Pg.192]    [Pg.164]    [Pg.170]    [Pg.201]    [Pg.77]    [Pg.53]    [Pg.1073]    [Pg.50]   
See also in sourсe #XX -- [ Pg.75 ]



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4-/-Butylcatechol

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