215734-58-0Relevant articles and documents
Iron-catalyzed Minisci acylation of N-heteroarenes with α-keto acids
Wang, Xiu-Zhi,Zeng, Cheng-Chu
, p. 1425 - 1430 (2019)
An efficient and mild protocol has been developed for the Minisci acylation reactions of nitrogen-containing heteroarenes with α-keto acids. Distinct from the conventional Minisci acylation conditions, the chemistry was performed using non-noble metal Fe(II), instead of expensive Ag(I) salt, as catalyst. A wide range of substrates, including aliphatic or aromatic α-keto acids, as well as various N-heteroarenes, proved to be compatible with the protocol. Scale-up experiment also demonstrates the practicality of the approach.
Fluorinated Quinoxalines: Synthesis and Alkylation
Mokrushina,Charushin,Shevelin,Chasovskikh,Shcherbakov,Aleksandrov,Chupakhin
, p. 109 - 114 (2007/10/03)
6,7-Difluoro- and 6-fluoro-7-morpholino(4-methylpiperazinyl, 2,6-dimethylpiperazinyl)quinoxalines have been synthesized from aromatic diamines and glyoxal, and their alkylation with Meerwein reagent has been studied. A procedure has been developed for preparation of pure 1-ethylquinoxalinium salts whose structure has been confirmed by 1H NMR spectra and X-ray analysis.