An article Electrochemical TEMPO-catalyzed multicomponent C(sp(3))-H alpha-carbamoylation of free cyclic secondary amines WOS:000496489100014 published article about OXIDATIVE UGI-TYPE; ANODIC CYANATION; DIRECT FUNCTIONALIZATION; TERTIARY-AMINES; BOND FORMATION; ELECTROSYNTHESIS; STRATEGIES; ARYLATION; NITRILES in [Pan, Na; Zapata, Ramiro; Pulicani, Jean-Pierre; Grimaud, Laurence] Sorbonne Univ, Ecole Normale Super, Lab Biomol, CNRS, 24 Rue Lhomond, F-75005 Paris, France; [Pan, Na] East China Normal Univ, SCME, Shanghai Engn Res Ctr Mol Therapeut & New Drug De, 3663 Zhongshanbei Rd, Shanghai 200062, Peoples R China; [Ling, Johanne; Vitale, Maxime R.] PSL Univ Paris, Chim ParisTech, CNRS, Inst Chem Hlth & Life Sci, 11 Rue Pierre & Marie Curie, F-75005 Paris, France in 2019, Cited 50. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1. Formula: C5H8O2
We report here an original electrosynthetic method allowing the straightforward C(sp(3))-H alpha-carbamoylation of free cyclic secondary amines. Based on a TEMPO-catalyzed indirect anodic oxidation and a multicomponent coupling, a wide variety of N-acyl alpha-carboxamides have been obtained under remarkably mild and sustainable reaction conditions.
Welcome to talk about 80-59-1, If you have any questions, you can contact Pan, N; Ling, J; Zapata, R; Pulicani, JP; Grimaud, L; Vitale, MR or send Email.. Formula: C5H8O2
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles