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Recent advances in radical-mediated intermolecular (4 + 2) cycloaddition.
Cai, Xue-Er; Wang, Zi-Ying; Tian, Wen-Chan; Liu, Hongxin; Wei, Wen-Ting; Lei, Ke-Wei.
Afiliação
  • Cai XE; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China. leikewei@nbu.edu.cn.
  • Wang ZY; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China. leikewei@nbu.edu.cn.
  • Tian WC; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China. leikewei@nbu.edu.cn.
  • Liu H; College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang, 325035, China. hongxin-107@163.com.
  • Wei WT; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China. leikewei@nbu.edu.cn.
  • Lei KW; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China. leikewei@nbu.edu.cn.
Org Biomol Chem ; 21(30): 6068-6082, 2023 Aug 02.
Article em En | MEDLINE | ID: mdl-37427565
ABSTRACT
(4 + 2) Cycloaddition plays an important role in the synthesis of versatile carbocyclic/heterocyclic compounds with its high atom- and step-economy. Additionally, with mild conditions and indispensable functional group compatibility, the radical reaction has been recognized as a useful tool in organic chemistry. Given the enormous impact of radical-mediated (4 + 2) cycloaddition processes and their promising applications, we summarize and highlight the recent works in this attractive area. On the basis of the types of radicals that initiate different (4 + 2) cycloaddition processes, we classify them into processes involving alkenyl cations or alkenyl radicals, aryl radicals, acyl radicals, alkyl radicals, and heteroatom radicals, and this review places special emphasis on the reaction design and mechanisms, which will stimulate future developments in radical-mediated intermolecular (4 + 2) cycloaddition.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article