Tin-mediated Radical Cyclization Reactions

Author:

malik Saima1,Lavekar Aditya G.2,Banik Bimal Krishna3

Affiliation:

1. Department of Chemistry, Panjab University, Sector-14, Chandigarh, India

2. Medicinal and Process Chemistry Division, CSIRCentral Drug Research Institute, Lucknow-226031, India

3. College of Sciences and Human Studies; Prince Mohammad Bin Fahd University, P.O. Box 1664; Al Khobar 31952, Saudi Arabia

Abstract

Radical chemistry is known for two centuries. Due to the fascinating nature of the radical-mediated processes, these reactions have attracted the attention of organic chemists to prepare new compounds with diverse stereochemistry. Radical-induced methods mostly follow atom economical principles. Tin-based radical annulation method is the most common and widely used procedure for the synthesis of a wide range of organic compounds with medicinal significance. In this review, we report recent stereoselective tin-mediated radical cyclization reactions. The versatility of tinbased reagents in the cyclization process as reported herein will encourage chemists to construct many other molecules of interest following the principles involved in these reactions.

Funder

University Grants Commission India

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Strategies for the Controlled Hydrostannylation of Alkynes;European Journal of Organic Chemistry;2023-09-27

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