Radical Reactions of Ynamides.

Small Methods

Key Laboratory for Chemical Biology of Fujian Province & State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.

Published: March 2021

AI Article Synopsis

  • Ynamides are special compounds featuring a C-C triple bond directly connected to an amide group, and they are useful in organic synthesis.
  • While ynamides are commonly used in ionic reactions, their radical-based reactions have not been explored as thoroughly.
  • This review focuses on radical reactions of ynamides, detailing their selectivity, mechanisms, and potential applications, aiming to enhance understanding and further research in ynamide chemistry.

Article Abstract

Ynamides are electron-rich heteroatom-substituted alkynes with C-C triple bond directly tethered to the amide group. Over the past decades, ynamides have proven to be versatile reagents for organic synthesis and have received extensive attention. Compared with the well-established ionic reactions of ynamides, radical-based ynamide reactions have been exploited relatively seldom. Herein, radical reactions of ynamides, classified by radical attack at the α-position and β-position of ynamides, are reviewed by highlighting the reaction selectivity, scope, mechanism, and applicability. The aim of this review is to provide a comprehensive summarization of these advances, casting light on the further development of ynamide chemistry.

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Source
http://dx.doi.org/10.1002/smtd.202000673DOI Listing

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