Xu, Yi-Xin; Liang, Yu-Qing; Cai, Zhong-Jian; Ji, Shun-Jun published an article in 2022. The article was titled 《Ruthenium(II)-Catalyzed Chelation-Assisted Desulfitative Arylation of Benzo[h]quinolines with Arylsulfonyl Chlorides》, and you may find the article in Organic Letters.Related Products of 98-60-2 The information in the text is summarized as follows:
Herein, a novel chelation-assisted C-H arylation reaction of benzo[h]quinoline is described. This transformation, using [RuCl2(p-cymene)]2 as the catalyst and cheap and easily accessible arylsulfonyl chlorides as the arylation source, featured simple reaction conditions, a broad substrate scope, and functional group tolerance. The successful application of some bioactive-mol.-based sulfonyl chlorides further highlighted the potential utility and importance of this desulfitative C-H arylation protocol. In the experiment, the researchers used 4-Chlorobenzenesulfonyl chloride(cas: 98-60-2Related Products of 98-60-2)
4-Chlorobenzenesulfonyl chloride(cas: 98-60-2) belongs to organochlorine compounds. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Related Products of 98-60-2
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics