Synthesis of a highly stable iron porphyrin coordinated by alkylthiolate anion as a model for cytochrome P-450 and its catalytic activity in O-O bond cleavage
Sulfide oxidation, amine N-demethylation, and olefin oxidation by heme-undecapeptide, microperoxidase-11, in the presence of hydrogen
Application of chemical P-450 model systems to study drug metabolism. III. Metabolism of 3-isobutyryl-2-isopropylpyrazolo [1,5-a] pyridine
Comparative study on drug metabolism using cyt. P450 chemical model and liver microsomal systems
"Metabolic activation" of o-methoxyphenols via O-demethylation with a Cu[2+]-ascorbic acid-O[2] system as a functional model of cytochrome P-450
Application of chemical cytochrome P-450 model systems to studies on drug metabolism. IV. Mechanism of piperidine metabolism pathways via an iminium intermediate
Substrate oxidation catalyzed by heme-undecapeptide, microperoxidase-11 in the presence of iodosylbenzene and cumene hydroperoxide
Highly efficient oxygen transfer reactions from various heteroaromatic N-oxides to olefins, alcohols, and sulfides catalyzed by ruthenium porphyrin
[18]O incorporation from H[2][18]O[2] in the oxidation of N-methylcarbazole and sulfides catalyzed by microperoxidase-11
The selectivities and the mechanism on highly efficient epoxidation of olefins with 2,6-disubstituted pyridine N-oxides catalyzed by ruthenium porphyrin