Quinoxaline-1, 2, 3-dithiazolyls Synthesis, EPR characterization, and redox chemistry
AW Cordes, JR Mingie, RT Oakley…
Index: Cordes; Mingie; Oakley; Reed; Zhang Canadian Journal of Chemistry, 2001 , vol. 79, # 9 p. 1352 - 1359
Full Text: HTML
Citation Number: 24
Abstract
Oxidation of quinoxalineaminothiol with SCl2 or S2Cl2/Cl2 affords a series of compounds based on the quinoxaline-1, 2, 3-dithiazole framework QDTA. Under highly oxidizing conditions, the 1, 2, 3-dithiazolyl ring is opened to afford the acyclic dichlorosulfimino- sulfenyl chlorides Cl x-QDTA-Cl3 (x= 0, 1, 2). Reduction of these" trichloro" compounds leads to ring closure. For x= 2, reduction using S2Cl2 affords the dithiazolylium chloride [ ...
Related Articles:
[Sonawane, Yogesh A.; Rajule, Rajkumar N.; Shankarling, Ganapati S. Monatshefte fur Chemie, 2010 , vol. 141, # 10 p. 1145 - 1151]
[Sonawane, Yogesh A.; Rajule, Rajkumar N.; Shankarling, Ganapati S. Monatshefte fur Chemie, 2010 , vol. 141, # 10 p. 1145 - 1151]
[Sonawane, Yogesh A.; Rajule, Rajkumar N.; Shankarling, Ganapati S. Monatshefte fur Chemie, 2010 , vol. 141, # 10 p. 1145 - 1151]
[Sonawane, Yogesh A.; Rajule, Rajkumar N.; Shankarling, Ganapati S. Monatshefte fur Chemie, 2010 , vol. 141, # 10 p. 1145 - 1151]