ChemInform Abstract: Oxidative Catalysis Using the Stoichiometric Oxidant as a Reagent: An Efficient Strategy for Single-Electron-Transfer-Induced Tandem Anion-Radical Reactions.

ChemInform ◽  
2015 ◽  
Vol 46 (9) ◽  
pp. no-no
Author(s):  
Frantisek Kafka ◽  
Martin Holan ◽  
Denisa Hidasova ◽  
Radek Pohl ◽  
Ivana Cisarova ◽  
...  
2020 ◽  
Vol 74 (1) ◽  
pp. 18-22
Author(s):  
Áron Péter ◽  
David J. Procter

This review focuses on recent developments from our laboratory in the field of radical reactions mediated by the archetypal reductive single electron transfer (SET) reagent, SmI2. Namely, we have expanded the scope of reducible carbonyl moieties to esters and amides and have exploited the resultant ketyl radicals in radical cascade reactions that generate unprecedented scaffolds. Moreover, we have taken the first steps to address the long-standing challenges of catalysis and chiral ligand control associated with the reagent.


2019 ◽  
Vol 21 (18) ◽  
pp. 7440-7444 ◽  
Author(s):  
Hongling Wang ◽  
Yuhuang Wang ◽  
Xingkuan Chen ◽  
Chengli Mou ◽  
Shuyan Yu ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yuki Matsuki ◽  
Nagisa Ohnishi ◽  
Yuki Kakeno ◽  
Shunsuke Takemoto ◽  
Takuya Ishii ◽  
...  

AbstractThere have been significant advancements in radical reactions using organocatalysts in modern organic synthesis. Recently, NHC-catalyzed radical reactions initiated by single electron transfer processes have been actively studied. However, the reported examples have been limited to catalysis mediated by alkyl radicals. In this article, the NHC organocatalysis mediated by aryl radicals has been achieved. The enolate form of the Breslow intermediate derived from an aldehyde and thiazolium-type NHC in the presence of a base undergoes single electron transfer to an aryl iodide, providing an aryl radical. The catalytically generated aryl radical could be exploited as an arylating reagent for radical relay-type arylacylation of styrenes and as a hydrogen atom abstraction reagent for α-amino C(sp3)–H acylation of secondary amides.


2020 ◽  
Vol 7 (16) ◽  
pp. 2349-2371 ◽  
Author(s):  
Dingwu Pan ◽  
Guihua Nie ◽  
Shichun Jiang ◽  
Tingting Li ◽  
Zhichao Jin

The background and recent breakthroughs in the single-electron-transfer (SET) reactions with trivalent tertiary phosphines are summarized and discussed in detail, and an outlook in the developments within this field is provided.


Author(s):  
Sundarababu Baskaran ◽  
Kirana D V ◽  
Kanak Kanti Das

A one-pot catalytic method has been developed for the stereoselective synthesis of cyclopropane-fused cyclic amidines using CuBr2/K2S2O8 as an efficient single electron transfer (SET) oxidative system. The generality of this...


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