4.7 Review

Nitriles as radical acceptors in radical cascade reactions

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 8, Issue 3, Pages 445-465

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0qo01058h

Keywords

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Funding

  1. National Natural Science Foundation of China [21501010, 21971224]
  2. 111 Project [D20003]
  3. Hunan Provincial Natural Science Foundation of China [2019JJ20008]

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The cyano group as a radical acceptor in cascade reactions offers diverse opportunities for the convenient construction of various important heterocycles and carbocycles, leading to the rapid buildup of molecular complexity. This review focuses on summarizing the dynamic field of radical cascade processes using the cyano group as a radical acceptor, which has not been well documented so far.
The cyano group is a valuable and readily available functional group for the preparation of various functional groups, such as amines, carboxylic acids, and ketones. In recent decades, the radical cascade reaction has emerged as a versatile tool to prepare a large variety of functional molecules. The application of the cyano group as a radical acceptor in cascade reactions provides diverse opportunities for the convenient construction of various important heterocycles and carbocycles. Such synthetic strategies will open new ways for the rapid buildup of molecular complexity. The focus of this review is the summary of the dynamic field of radical cascade processes using the cyano group as a radical acceptor, which has not been well documented so far.

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