CuCl-catalyzed aerobic oxidative reaction of primary aromatic amines
作者:Wenchao Lu、Chanjuan Xi
DOI:10.1016/j.tetlet.2008.04.089
日期:2008.6
The oxidations of primaryaromaticamines were investigated. Cuprous chloride-air system can catalyze the oxidation of primaryaromaticamines to azo derivatives, anils, and/or quinone anils. The experimental procedure is simple and the products could be easily isolated in high yields.
Oxidation of aromatic amines with chromyl chloride-I
作者:C. Nallaiah、J.A. Strickson
DOI:10.1016/s0040-4020(01)87565-7
日期:1986.1
The oxidation of aromaticprimaryamines with chromyl chloride in carbon tetrachloride or chloroform, results in the formation of intermediate solid adducts (Etard adducts) which, on hydrolysis, give azobenzenes(1), 1,4-benzoquinones(2),anilino-1,4-benzoquinones(3), 1,4-benzoquinone anils(4)and anilino-1,4-benzoquinone anils (5) in yields which depend on the position, nature and degree of substitution
NALLAIAH C.; STRICKSON J. A., TETRAHEDRON, 42,(1986) N 14, 4083-4087
作者:NALLAIAH C.、 STRICKSON J. A.
DOI:——
日期:——
HEDAYATULLAH M.; DECHATRE J. P.; DENIVELLE L., TETRAHEDRON LETT. <TELE-AY>, 1975, NO 25, 2039-2042
作者:HEDAYATULLAH M.、 DECHATRE J. P.、 DENIVELLE L.
DOI:——
日期:——
Iodination of Anilines with Sodium Dichloroiodate
作者:Shire Elmi、Per Heggen、Bjarte Holmelid、Didrik Malthe-Sørensen、Leiv K. Sydnes
DOI:10.1080/00304948.2016.1206425
日期:2016.9.2
conditions 2a was not formed at all and a complex product mixture was obtained from which the only reasonably pure product isolated in low yield (4%) was 2,20,4,40-tetramethylazobenzene (3a). The iodination of benzene derivatives is influenced by the nature of the substituents. It was therefore of interest to investigate the reaction of some activated and deactivated aniline derivatives under the conditions