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Combining Enzyme and Photoredox Catalysis for the Construction of 3-Aminoalkyl Chromones.
Hu, Jia-Yu; Xie, Zong-Bo; Tang, Juan; Le, Zhang-Gao; Zhu, Zhi-Qiang.
Afiliação
  • Hu JY; Jiangxi Province Key Laboratory of Synthetic Chemistry, School of Chemistry, Biology and Material Science, East China University of Technology, Nanchang 330013, PR China.
  • Xie ZB; Jiangxi Province Key Laboratory of Synthetic Chemistry, School of Chemistry, Biology and Material Science, East China University of Technology, Nanchang 330013, PR China.
  • Tang J; Ministry of Education Key Laboratory of Functional Small Organic Molecule, Department of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, PR China.
  • Le ZG; Jiangxi Province Key Laboratory of Synthetic Chemistry, School of Chemistry, Biology and Material Science, East China University of Technology, Nanchang 330013, PR China.
  • Zhu ZQ; Jiangxi Province Key Laboratory of Synthetic Chemistry, School of Chemistry, Biology and Material Science, East China University of Technology, Nanchang 330013, PR China.
J Org Chem ; 87(21): 14965-14969, 2022 11 04.
Article em En | MEDLINE | ID: mdl-36279475
ABSTRACT
Herein, we reported a practical and efficient strategy combining photoredox and enzyme catalysis for the construction of 3-aminoalkyl chromones from o-hydroxyaryl enaminones and N-arylglycine esters. A variety of 3-aminoalkyl chromones were synthesized with good yields under mild conditions in one pot. This synthetic protocol consists of sequential enzymatic hydrolysis and photoredox decarboxylation of N-arylglycine esters, oxidation of aminoalkyl radicals, Mannich reaction, and intramolecular nucleophilic cyclization, which affords a convenient pathway for the preparation of various 3-substituted chromones.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromonas / Ésteres Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromonas / Ésteres Idioma: En Ano de publicação: 2022 Tipo de documento: Article