Tetrahedron letters

A mild oxidation of aromatic amines

KS Webb, V Seneviratne

Index: Webb, Kevin S.; Seneviratne, Viran Tetrahedron Letters, 1995 , vol. 36, # 14 p. 2377 - 2378

Full Text: HTML

Citation Number: 39

Abstract

Several primary aromatic amines have been converted to the corresponding nitro compounds in good yields. The oxidant was oxone®(potassium peroxymonosulfate) and the reactions were performed in 5 to 20% aqueous acetone and buffered with sodium bicarbonate.

Related Articles:

An in-depth study of the biotransformation of nitriles into amides and/or acids using Rhodococcus rhodochrous AJ270 1

[Meth-Cohn, Otto; Wang, Mei-Xiang Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 8 p. 1099 - 1104]

Facile and Chemoselective Cleavage of Allyl Carboxylic Ester Utilizing NaBH4 in DMSO

[Pawar, Bharati V.; Lokhande, Pradeep D. Synthetic Communications, 2009 , vol. 39, # 14 p. 2445 - 2453]

An efficient method for one-carbon elongation of aryl aldehydes via their dibromoalkene derivatives

[Huh, Dal Ho; Jeong, Ji Sang; Lee, Hee Bong; Ryu, Hoejin; Kim, Young Gyu Tetrahedron, 2002 , vol. 58, # 50 p. 9925 - 9932]

Electrophilic aromatic substitution with N-methoxy-N-acylnitrenium ions generated from N-chloro-N-methoxy amides: syntheses of nitrogen heterocyclic compounds …

[Journal of Organic Chemistry, , vol. 54, # 14 p. 3394 - 3403]

Hydrolysis of esters and amides in strongly basic solution. Evidence for the intermediacy of carbanions

[Journal of Organic Chemistry, , vol. 46, # 6 p. 1186 - 1191]

More Articles...