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PPh3-Triggered Tandem Synthesis of 2,3-Disubstituted Benzofuran Derivatives from o-Quinone Methides with Acyl Chlorides.
Ma, Yu-Hong; He, Xiao-Yu; Wang, Long; Yang, Qing-Qing.
Afiliação
  • Ma YH; College of Materials and Chemical Engineering, Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials, China Three Gorges University, 8 Daxue Road, Yichang, Hubei 443002, People's Republic of China.
  • He XY; College of Materials and Chemical Engineering, Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials, China Three Gorges University, 8 Daxue Road, Yichang, Hubei 443002, People's Republic of China.
  • Wang L; College of Materials and Chemical Engineering, Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials, China Three Gorges University, 8 Daxue Road, Yichang, Hubei 443002, People's Republic of China.
  • Yang QQ; Hubei Three Gorges Labratory, Yichang, Hubei 443007, People's Republic of China.
J Org Chem ; 87(17): 11852-11856, 2022 09 02.
Article em En | MEDLINE | ID: mdl-35960255
ABSTRACT
A PPh3-triggered tandem strategy for the efficient synthesis of valuable 2,3-disubstituted benzofuran derivatives in generally good to high yields from aryl or alkyl acyl chlorides and o-quinone methides has been developed. This method features mild reaction conditions, simple operation, and a broad substrate scope.
Assuntos

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

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