《Palladium Catalyzed Aminocarbonylation of Benzylic Ammonium Triflates with Nitroarenes: Synthesis of Phenylacetamides》 was written by Yang, Li-Miao; Li, Shan-Shan; Zhang, You-Ya; Lu, Jin-Liang; Deng, Jing-Tong; Ma, Ai-Jun; Zhang, Xiang-Zhi; Zhang, Shu-Yu; Peng, Jin-Bao. Recommanded Product: 350-30-1 And the article was included in Advanced Synthesis & Catalysis on April 17 ,2021. The article conveys some information:
A palladium catalyzed reductive aminocarbonylation of benzylic ammonium triflates with nitroarenes for the synthesis of phenylacetamides was developed. Using Pd(acac)2/DPPF catalyst system, a range of different substituted phenylacetamides were prepared in moderate to good yields from benzylic ammonium triflates and nitroarenes through Csp3-N bond cleavage. A variety of alkyl, aryl, and halide substituents on both substrates was used, and many useful functional groups were tolerated. In the experiment, the researchers used many compounds, for example, 3-Chloro-4-fluoronitrobenzene(cas: 350-30-1Recommanded Product: 350-30-1)
3-Chloro-4-fluoronitrobenzene(cas: 350-30-1) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Recommanded Product: 350-30-1
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics