Recent advances in cascade radical cyclization of radical acceptors for the synthesis of carbo- and heterocycles

Literature Information

Publication Date 2021-01-08
DOI 10.1039/D0QO01453B
Impact Factor 5.281
Authors

Jianhua Liao, Xiao Yang, Lu Ouyang, Yinlong Lai, Jiuzhong Huang, Renshi Luo


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Abstract

Cascade radical cyclization is an attractive synthetic method due to its high atom- and step-economy to construct carbo- and heterocycles, which have wide applications in chemical and life science industries. Radical acceptors with unsaturated bonds play a key role in realizing highly rapid, concise, and efficient cascade radical cyclization. This Review is devoted to highlighting the latest achievements in the development of cascade radical cyclization methodologies for the synthesis of carbo- and heterocycles in this rapidly growing research field. Based on the hybridization of starting materials, this Review includes C(sp)–C(sp) bond, C(sp)–C(sp2) bond, C(sp2)–C(sp2) bond, C(sp2)–C(sp3), and carbon–heteroatom bond coupling cyclization. Representative examples mainly published in last three years will be discussed for each highlighted reaction design and mechanism, providing readers with common tools for future research in cascade radical cyclization.

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Source Journal

Organic Chemistry Frontiers

Organic Chemistry Frontiers
CiteScore: 7.8
Self-citation Rate: 8.7%
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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