J. Barry Noar

Monooxygen donation potential of 4a-hydroperoxyflavins as compared with those of a percarboxylic acid and other hydroperoxides. Monooxygen donation to olefin, tertiary amine, alkyl sulfide, and iodide ion

Thomas C. Bruice, J. Barry Noar, Sheldon S. Ball et al. · Journal of the American Chemical Society · 1983 · 105 citations

Natural Sciences, Biochemistry, Chemistry +5

Synthesis of 7,9-didecarboxymethoxatin (4,5-dihydro-4,5-dioxo-1H-pyrrolo[2,3-f]quinoline-2-carboxylic acid) and comparison of its chemical properties with those of methoxatin and analogous o-quinones. Model studies directed toward the action of PQQ requiring bacterial oxidoreductases and mammalian plasma amine oxidase

Paul R. Sleath, J. Barry Noar, Gert Eberlein et al. · Journal of the American Chemical Society · 1985 · 82 citations

Life Sciences, Biochemistry, Chemistry +9

Synthesis of 9-decarboxymethoxatin. Metal complexation of methoxatin as a possible requirement for its biological activity

J. Barry Noar, Evelyn J. Rodriguez, Thomas C. Bruice · Journal of the American Chemical Society · 1985 · 52 citations

Natural Sciences, Chemistry, Medicinal Chemistry +6

Oxidation of N-nitrosodibenzylamine and related compounds by metalloporphyrin-catalysed model systems for the cytochrome P450 dependent mono-oxygenases

John R. Lindsay Smith, Michael W. Nee, J. Barry Noar et al. · Journal of the Chemical Society Perkin Transactions 2 · 1984 · 14 citations

Life Sciences, Biochemistry, Chemistry +17

The possibility that the spectrum of intermediate two, seen in the course of reaction of flavoenzyme phenol hydroxylases, may be attributable to iminol isomers of a flavin-derived 6-arylamino-5-oxo(3H,5H)uracil.

Albert Wessiak, J. Barry Noar, Thomas C. Bruice · Proceedings of the National Academy of Sciences · 1984 · 13 citations · Full text

Pharmacy, Biochemistry, Chemistry +7