Nitriles as radical acceptors in radical cascade reactions

Author(s):  
Kai Sun ◽  
Qi-Yan Lv ◽  
Ying-Wu Lin ◽  
Bing Yu ◽  
Wei-Min He

The application of the cyano group as a radical acceptor in the cascade reactions for the construction of various important heterocycles and carbocycles was summarized.

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.


2018 ◽  
Vol 16 (47) ◽  
pp. 9223-9229 ◽  
Author(s):  
Chen Zhang ◽  
Junxia Pi ◽  
Lei Wang ◽  
Ping Liu ◽  
Peipei Sun

A cyclization cascade initiated by the addition of a silyl radical to an electron-deficient carbon–carbon double bond of N-arylacrylamides, followed by intramolecular cyano group insertion and homolytic aromatic substitution has been reported.


1999 ◽  
Vol 121 (51) ◽  
pp. 12190-12191 ◽  
Author(s):  
Ilhyong Ryu ◽  
Hiroki Kuriyama ◽  
Satoshi Minakata ◽  
Mitsuo Komatsu ◽  
Joo-Yong Yoon ◽  
...  

Tetrahedron ◽  
2013 ◽  
Vol 69 (36) ◽  
pp. 7699-7705 ◽  
Author(s):  
Marie-Hélène Larraufie ◽  
Max Malacria ◽  
Christine Courillon ◽  
Cyril Ollivier ◽  
Louis Fensterbank ◽  
...  

ChemInform ◽  
2007 ◽  
Vol 38 (28) ◽  
Author(s):  
Matthew L. Maddess ◽  
Emily Mainetti ◽  
Youssef Harrak ◽  
Celia Brancour ◽  
Priscille Devin ◽  
...  

Synlett ◽  
1999 ◽  
Vol 1999 (9) ◽  
pp. 1462-1464 ◽  
Author(s):  
Philippe Renaud ◽  
Laura Andrau ◽  
Kurt Schenk

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