1383986-85-3Relevant academic research and scientific papers
Synthesis of Quinoxaline Derivatives via Tandem Oxidative Azidation/Cyclization Reaction of N -Arylenamines
Ma, Haichao,Li, Dianjun,Yu, Wei
, p. 868 - 871 (2016)
A new method was developed for the synthesis of quinoxalines. This method employs N-arylenamines and TMSN3 as the starting materials and implements two oxidative C-N bond-forming processes in a tandem pattern by using (diacetoxyiodo)benzene as the common oxidant. The present reaction conditions are mild and simple and thus are useful in practical synthesis. (Chemical Equation Presented).
Copper-Mediated One-Pot Synthesis of Indoles through Sequential Hydroamination and Cross-Dehydrogenative Coupling Reaction
Cai, Yichao,Chen, Chunxia,Chen, Xin,Liu, Yajie,Peng, Jinsong,Song, Zirui,Sun, Peng,Yang, Jiaojiao
, p. 75 - 84 (2019/12/26)
Starting from simple anilines and ester arylpropiolates, an efficient one-pot synthesis of 2-arylindole-3-carboxylate derivatives has been developed through copper-mediated sequential hydroamination and cross-dehydrogenative coupling (CDC) reaction. The i
Regiospecific Hydroamination of Unsymmetrical Electron-Rich and Electron-Poor Alkynes with Anilines Catalyzed by Gold(I) Immobilized in MCM-41
Liu, Dayi,Nie, Quan,Zhang, Rongli,Cai, Mingzhong
supporting information, p. 3940 - 3948 (2018/09/14)
The first heterogeneous gold(I)-catalyzed regiospecific hydroamination of ynamides and propiolic acid derivatives with anilines has been achieved by using a diphenylphosphine-functionalized MCM-41-supported gold (I) complex and AgNTf2 as catalysts under mild conditions, yielding the corresponding (E)-N-arylimines and (Z)-enamines in good to excellent yields with broad substrate scope. The new heterogeneous gold(I) complex can easily be prepared via a two-step procedure from commercially available reagents and recovered by simple filtration of the reaction mixture. The recovered catalyst (Ph2P-MCM-41-AuNTf2) can be reused at least seven times without addition of AgNTf2 as a co-catalyst and its catalytic efficiency remains unaltered. (Figure presented.).
Synthesis of chiral β-amino acid derivatives by asymmetric hydrosilylation with an imidazole derived organocatalyst
Jones, Simon,Li, Xianfu
experimental part, p. 5522 - 5532 (2012/09/21)
The organocatalysed asymmetric hydrosilylation of a number of N-aryl and alkyl β-substituted enamino esters proceeds in generally good yield and enantioselectivity. Crucial to obtaining high yield and selectivity was the addition of benzoic acid as an additive and under these conditions, both N-alkyl and N-aryl substituents were well tolerated. β-Aryl and alkyl substituents were evaluated and a model proposed to account for the experimental observations based upon enamine tautomerisation and conformational preferences of the reactive ketimine intermediate.
