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Visible light-induced selenylative spirocyclization of biaryl ynones toward the formation of selenated spiro[5.5]trienones.
Chen, Zhichao; Zheng, Xinran; Zhou, Shu-Feng; Cui, Xiuling.
Afiliação
  • Chen Z; College of Chemical Engineering, Huaqiao University, Xiamen, Fujian 361021, P. R. China. szhou@hqu.edu.cn.
  • Zheng X; Engineering Research Centre of Molecular Medicine of Ministry of Education, Key Laboratory of Fujian Molecular Medicine, Key Laboratory of Precision Medicine and Molecular Diagnosis of Fujian Universities, Key Laboratory of Xiamen Marine and Gene Drugs, School of Biomedical Sciences, Huaqiao Univers
  • Zhou SF; College of Chemical Engineering, Huaqiao University, Xiamen, Fujian 361021, P. R. China. szhou@hqu.edu.cn.
  • Cui X; Engineering Research Centre of Molecular Medicine of Ministry of Education, Key Laboratory of Fujian Molecular Medicine, Key Laboratory of Precision Medicine and Molecular Diagnosis of Fujian Universities, Key Laboratory of Xiamen Marine and Gene Drugs, School of Biomedical Sciences, Huaqiao Univers
Org Biomol Chem ; 20(29): 5779-5783, 2022 07 27.
Article em En | MEDLINE | ID: mdl-35815996
ABSTRACT
A visible-light induced dearomative cascade cyclization of biaryl ynones with diselenides under photocatalyst and external additive-free conditions has been explored, giving a series of selenated spiro[5.5]trienones in moderate to good yields. The Se-Se bond in diselenides could be cleaved to generate arylselenyl radicals under visible light irradiation in the absence of a photocatalyst. This protocol provides a facile and green method for the synthesis of spiro[5.5]trienones.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Espiro Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Espiro Idioma: En Ano de publicação: 2022 Tipo de documento: Article