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Zn(OTf)2-catalyzed intra- and intermolecular selenofunctionalization of alkenes under mild conditions.
Qi, Cong; Lu, Zhaogong; Gu, Yuyang; Bao, Xiaofeng; Xiong, Biao; Liu, Gong-Qing.
Afiliação
  • Qi C; School of Pharmacy, Nantong Key Laboratory of Small Molecular Drug Innovation, Nantong University Nantong 226019 People's Republic of China gqliu@ntu.edu.cn.
  • Lu Z; School of Pharmacy, Nantong Key Laboratory of Small Molecular Drug Innovation, Nantong University Nantong 226019 People's Republic of China gqliu@ntu.edu.cn.
  • Gu Y; School of Medicine, Nantong University Nantong 226019 People's Republic of China.
  • Bao X; School of Pharmacy, Nantong Key Laboratory of Small Molecular Drug Innovation, Nantong University Nantong 226019 People's Republic of China gqliu@ntu.edu.cn.
  • Xiong B; School of Pharmacy, Nantong Key Laboratory of Small Molecular Drug Innovation, Nantong University Nantong 226019 People's Republic of China gqliu@ntu.edu.cn.
  • Liu GQ; School of Pharmacy, Nantong Key Laboratory of Small Molecular Drug Innovation, Nantong University Nantong 226019 People's Republic of China gqliu@ntu.edu.cn.
RSC Adv ; 14(32): 23147-23151, 2024 Jul 19.
Article em En | MEDLINE | ID: mdl-39040696
ABSTRACT
Zn(OTf)2-catalyzed intra- and intermolecular selenofunctionalization of alkenes was achieved with electrophilic N-phenylselenophthalimide. This method provides straightforward and efficient access to various seleno-substituted heterocycles and vicinal Se heteroatom-disubstituted molecules under mild conditions. This reaction is compatible with various substrates/functional groups, and preliminary studies on the reaction mechanistic were also conducted.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2024 Tipo de documento: Article