TfOH-Catalyzed [4 + 1] Annulation of <i>p</i>-Quinone Methides with &#945;-Aryl Diazoacetates: Straightforward Access to Highly Functionalized 2,3-Dihydrobenzofurans.

Lu, Zuolin; Zhang, Qingchun; Ke, Miaolin; Hu, Sha; Xiao, Xiao; Chen, Fener

TfOH-Catalyzed [4 + 1] Annulation of p-Quinone Methides with α-Aryl Diazoacetates: Straightforward Access to Highly Functionalized 2,3-Dihydrobenzofurans.

Lu, Zuolin; Zhang, Qingchun; Ke, Miaolin; Hu, Sha; Xiao, Xiao; Chen, Fener.

Afiliação

Lu Z; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, P.R. China.
Zhang Q; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, P.R. China.
Ke M; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, P.R. China.
Hu S; Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, Shanghai 200433, P.R. China.
Xiao X; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, P.R. China.
Chen F; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, P.R. China.

J Org Chem ; 86(11): 7625-7635, 2021 06 04.

Article em En | MEDLINE | ID: mdl-33993694

Assuntos

Benzofuranos; Indolquinonas; Catálise

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzofuranos / Indolquinonas Idioma: En Revista: J Org Chem Ano de publicação: 2021 Tipo de documento: Article

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