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- W2950863090 abstract "4-Phenylphenoxazinones 4 were isolated after biomimetic oxidation, using diphenoloxidases of insect cuticle, mushroom tyrosinase, or after autoxidation of N-acetyldopamine (1) in the presence of β-alanine, β-alanine methyl ester or N-acetyl-L-lysine. They are formed presumably by addition of 2-aminoalkyl-5-alkylphenols 2 to the o-quinone of biphenyltetrol 3 which, in turn, arises from oxidative coupling of 1. The structures of 4 present the first examples for the assembly of reasonably stable intermediates in the rather complex process of chemical modifications of aliphatic amino acid residues by o-quinones." @default.
- W2950863090 created "2019-06-27" @default.
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- W2950863090 date "2010-08-21" @default.
- W2950863090 modified "2023-09-25" @default.
- W2950863090 title "ChemInform Abstract: Catecholamine-Protein Conjugates: Isolation of 4-Phenylphenoxazin-2- ones from Oxidative Coupling of N-Acetyldopamine with Aliphatic Amino Acids." @default.
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- W2950863090 doi "https://doi.org/10.1002/chin.199306059" @default.
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