Radicals Masquerading as Electrophiles: Dual Orbital Effects in Nitrogen-Philic Acyl Radical Cyclization and Related Addition Reactions

2007 ◽  
Vol 40 (5) ◽  
pp. 303-313 ◽  
Author(s):  
Carl H. Schiesser ◽  
Uta Wille ◽  
Hiroshi Matsubara ◽  
Ilhyong Ryu
ChemInform ◽  
2011 ◽  
Vol 42 (13) ◽  
pp. no-no
Author(s):  
Ken-ichi Yamada ◽  
Tomohiro Sato ◽  
Masaki Hosoi ◽  
Yasutomo Yamamoto ◽  
Kiyoshi Tomioka

2005 ◽  
Vol 70 (2) ◽  
pp. 681-683 ◽  
Author(s):  
Kazuya Yoshikai ◽  
Tomoharu Hayama ◽  
Katsumi Nishimura ◽  
Ken-ichi Yamada ◽  
Kiyoshi Tomioka

ChemInform ◽  
2006 ◽  
Vol 37 (35) ◽  
Author(s):  
Seth W. Grant ◽  
Koudi Zhu ◽  
Yu Zhang ◽  
Steven L. Castle

2005 ◽  
Vol 53 (5) ◽  
pp. 586-588 ◽  
Author(s):  
Kazuya Yoshikai ◽  
Tomoharu Hayama ◽  
Katsumi Nishimura ◽  
Ken-ichi Yamada ◽  
Kiyoshi Tomioka

Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6843
Author(s):  
Xiang-Kui He ◽  
Juan Lu ◽  
Hai-Bing Ye ◽  
Lei Li ◽  
Jun Xuan

An acyl radical generation and functionalization strategy through direct photoexcitation of benzothiazolines has been developed. The formed acyl radical species can either be trapped by quinoxalin-2-ones to realize their C(3)-H functionalization or trigger a cascade radical cyclization with isonitriles to synthesise biologically important phenanthridines. The synthetic value of this protocol can be further illustrated by the modification of quinoxalin-2-ones, containing important natural products and drug-based complex molecules.


1997 ◽  
Vol 548 (1) ◽  
pp. 105-107 ◽  
Author(s):  
Ilhyong Ryu ◽  
Kiyoto Nagahara ◽  
Akio Kurihara ◽  
Mitsuo Komatsu ◽  
Noboru Sonoda

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