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How Chemical Environment Activates Anthralin and Molecular Oxygen for Direct Reaction.
Ellis, Emerald S; MacHale, Luke T; Szilagyi, Robert K; DuBois, Jennifer L.
Afiliação
  • Ellis ES; Department of Chemistry and Biochemistry , Montana State University , P.O. Box 173400, Bozeman , Montana 59717 , United States.
  • MacHale LT; Department of Chemistry and Biochemistry , Montana State University , P.O. Box 173400, Bozeman , Montana 59717 , United States.
  • Szilagyi RK; Department of Chemistry and Biochemistry , Montana State University , P.O. Box 173400, Bozeman , Montana 59717 , United States.
  • DuBois JL; Department of Chemistry and Biochemistry , Montana State University , P.O. Box 173400, Bozeman , Montana 59717 , United States.
J Org Chem ; 85(2): 1315-1321, 2020 01 17.
Article em En | MEDLINE | ID: mdl-31830417
The role of the chemical environment in promoting anthralin/O2 reactions was discovered using neat solvents to model the amino acids of a cofactor-independent oxygenase. Experimental and computational results highlight the importance of the substrate-enolate, which is accessed via energetically small, escalating steps in which the ground-state keto-isomer is tautomerized to an enol and then ionized by solvent. The resulting ion-pair is poised for spontaneous electron transfer to O2. Similar activation may be exploited in biological/nonbiological oxidations involving O2.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos