Direct Conversion of Arylamines to the Halides by Deamination with Thionitrite or Related Compounds and Anhydrous Copper(II) Halides
作者:Shigeru Oae、K\={o}ichi Shinhama、Yong Hae Kim
DOI:10.1246/bcsj.53.1065
日期:1980.4
Reactions of various arylamines with either t-butyl thionitrite, t-butyl thionitrate, or p-toluenesulfonyl nitrite in the presence of anhydrous copper(II) halides under mild conditions gave corresponding aryl halides in good yields. This reaction in the presence of such olefins as acrylonitrile, styrene, and acrylic acid gave the corresponding 2-aryl-1-haloethanes as the main products. t-Butyl thionitrite
在无水卤化铜 (II) 存在下,各种芳基胺与亚硫硝酸叔丁酯、亚硫硝酸叔丁酯或对甲苯磺酰亚硝酸酯在温和条件下反应,以良好的收率得到相应的芳基卤化物。在丙烯腈、苯乙烯和丙烯酸等烯烃存在下,该反应得到相应的 2-芳基-1-卤代乙烷作为主要产物。由于硫-氮键较弱,亚硝酸叔丁酯、亚硝酸叔丁酯和对甲苯磺酰亚硝酸酯是比亚硝酸烷基酯或硝酸烷基酯更好的脱氨基试剂。
Formation of quaternary carbons through cobalt-catalyzed C(sp<sup>3</sup>)–C(sp<sup>3</sup>) Negishi cross-coupling
作者:Eduardo Palao、Enol López、Iván Torres-Moya、Antonio de la Hoz、Ángel Díaz-Ortiz、Jesús Alcázar
DOI:10.1039/d0cc02734k
日期:——
quaternary carbons is a key challenge in organic and medicinal chemistry. We report a cobalt-catalyzed C(sp3)–C(sp3) cross-coupling that allows for the introduction of benzyl, heteroarylmethylzinc and allyl groups to halo-carbonyl substrates. The cross-coupling reaction is selective for C(sp3)-over C(sp2)-halides, in contrast to most used catalytic metals, and allows access to novel scaffolds of pharmaceutical
An olefin, especially an activated olefin, is arylated by reaction with an arylamine, such as an aniline, in an inert polar organic solvent and in the presence of an alkyl nitrite, a hydrogen halide, and a catalytic amount of a copper catalyst having the copper in an oxidation state below +2.