An ESR study of thiyl radical addition at the carbonyl group

Author(s):  
R. G. Gasanov ◽  
R. G. Petrova ◽  
I. O. Bragina ◽  
R. Kh. Freidlina
2003 ◽  
Vol 14 (19) ◽  
pp. 2853-2856 ◽  
Author(s):  
Gregory K. Friestad ◽  
Tao Jiang ◽  
Gina M. Fioroni

2009 ◽  
Vol 11 (12) ◽  
pp. 2651-2654 ◽  
Author(s):  
Habibur Rahaman ◽  
Masafumi Ueda ◽  
Okiko Miyata ◽  
Takeaki Naito

ChemInform ◽  
2004 ◽  
Vol 35 (7) ◽  
Author(s):  
Gregory K. Friestad ◽  
Tao Jiang ◽  
Gina M. Fioroni

2017 ◽  
Vol 15 (35) ◽  
pp. 7330-7338 ◽  
Author(s):  
Yan-qin Yuan ◽  
Pailla Santhosh Kumar ◽  
Chun-niu Zhang ◽  
Ming-hua Yang ◽  
Sheng-rong Guo

A highly effective dioxygen-triggered oxidative thiyl radical addition/cyclization of N-methacryloylbenzamides was explored. This method provides convenient access to a variety of useful sulfide-containing 4,4-disubstituted isoquinoline-1,3-diones.


Sign in / Sign up

Export Citation Format

Share Document