Infrared and Electronic Spectra of Radicals Produced from 2-Naphthol and Carbazole by UV-Induced Hydrogen-Atom Eliminations

2012 ◽  
Vol 116 (36) ◽  
pp. 8980-8988 ◽  
Author(s):  
Masahiko Sekine ◽  
Hiroshi Sekiya ◽  
Munetaka Nakata
1976 ◽  
Vol 73 ◽  
pp. 523-526 ◽  
Author(s):  
Vinicio Galasso ◽  
Giuseppe C. Pappalardo ◽  
Giuseppe Scarlata
Keyword(s):  

1982 ◽  
Vol 138 (10) ◽  
pp. 347 ◽  
Author(s):  
Yurii L. Sokolov ◽  
V.P. Yakovlev
Keyword(s):  

2019 ◽  
Author(s):  
Shiori Date ◽  
Kensei Hamasaki ◽  
Karen Sunagawa ◽  
Hiroki Koyama ◽  
Chikayoshi Sebe ◽  
...  

<div>We report here a catalytic, Markovnikov selective, and scalable synthetic method for the synthesis of saturated sulfur heterocycles, which are found in the structures of pharmaceuticals and natural products, in one step from an alkenyl thioester. Unlike a potentially labile alkenyl thiol, an alkenyl thioester is stable and easy to prepare. The powerful Co catalysis via a cobalt hydride hydrogen atom transfer and radical-polar crossover mechanism enabled simultaneous cyclization and deprotection. The substrate scope was expanded by the extensive optimization of the reaction conditions and tuning of the thioester unit.</div>


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