Expanding Pd-Catalyzed C-N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions. [Erratum to document cited in CA139:117168] was written by Huang, Xiaohua;Anderson, Kevin W.;Zim, Danilo;Jiang, Lei;Klapars, Artis;Buchwald, Stephen L.. And the article was included in Journal of the American Chemical Society in 2003.Quality Control of tert-Butyl (4-chlorophenyl)carbamate This article mentions the following:
An important reference pertinent to the Pd-catalyzed amination in water was omitted on page 6655. The work by Boche and co-workers (Wullner, G.; Jansch, H.; Kannenberg, S.; Schubert, F.; Boche, G. Chem. Commun. 1998, 1509-1510) describes one example of aryl amination in water and several examples of aryl amination in aqueous solvent mixtures using NaOH as base. In the experiment, the researchers used many compounds, for example, tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6Quality Control of tert-Butyl (4-chlorophenyl)carbamate).
tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Quality Control of tert-Butyl (4-chlorophenyl)carbamate
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics