Oxidation of arylthiourea by cetyltrimethylammonium dichromate

…, PR Sahoo, S Patel, BK Mishra

Index: Sahu, Sandhyamayee; Sahoo, Prangya Rani; Patel, Sabita; Mishra Synthetic Communications, 2010 , vol. 40, # 21 p. 3268 - 3273

Full Text: HTML

Citation Number: 8

Abstract

With a view to investigate the oxidation behaviors of cetyltrimethylammonium dichromate on multifunctional groups, some arylthioureas were subjected to oxidation, both in neutral and in acidic conditions. In neutral conditions, the products were found to be a mixture of corresponding urea and isonitrile. In acidic conditions, the products were corresponding ureas only. A probable mechanism was proposed for the formation of the product, wherein ...

Related Articles:

Phenylureas. Part 1. Mechanism of the basic hydrolysis of phenylureas

[Laudien; Mitzner Journal of the Chemical Society, Perkin Transactions 2, 2001 , # 11 p. 2226 - 2229]

Synthesis and anticonvulsant activity of halo-substituted aryl urea and thioureas

[Gupta, Mahesh Kumar; Pandeya, Suerendra N.; Zaiad, Golal M.; Gangwar Journal of the Indian Chemical Society, 2010 , vol. 87, # 11 p. 1421 - 1424]

3??(1??Hydroxyalkyl)??1, 4, 2??dioxazol??5??one und 3??Hydroxyoxazolidin??2, 4??dione aus 2??Hydroxycarbohydroxamsäuren und 1, 1′??Carbonyldiimidazol1a)

[Geffken, Detlef Liebigs Annalen der Chemie, 1982 , # 2 p. 211 - 218]

Kinetics and mechanism of methanolysis of benzoyl derivatives of substituted phenylureas and phenylthioureas

[Kavalek, Jaromir; El Bahaie, Said; Sterba, Vojeslav Collection of Czechoslovak Chemical Communications, 1984 , vol. 49, # 9 p. 2103 - 2110]

More Articles...