Qu, Erdong; Li, Shangzhang; Bai, Jin; Zheng, Yan; Li, Wanfang published the artcile< Nickel-Catalyzed Reductive Cross-Coupling of N-Acyl and N-Sulfonyl Benzotriazoles with Diverse Nitro Compounds: Rapid Access to Amides and Sulfonamides>, Category: chlorides-buliding-blocks, the main research area is amide preparation; acyl benzotriazole nitro compound reductive cross coupling nickel catalyzed; sulfonamide preparation; sulfonyl benzotriazole nitro compound reductive cross coupling nickel catalyzed.
Herein, a Ni-catalyzed reductive transamidation of conveniently available N-acyl benzotriazoles with alkyl, alkenyl and aryl nitro compounds, which afforded various amides with good yields and a broad substrate scope was reported. The same catalytic reaction conditions were also applicable for N-sulfonyl benzotriazoles, which could undergo smooth reductive coupling with nitroarenes and nitroalkanes to afford the corresponding sulfonamides.
Organic Letters published new progress about Amides Role: SPN (Synthetic Preparation), PREP (Preparation). 17082-09-6 belongs to class chlorides-buliding-blocks, and the molecular formula is C9H7ClO, Category: chlorides-buliding-blocks.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics