4138-37-8Relevant articles and documents
A reductive amination of carbonyls with amines using decaborane in methanol
Bae, Jong Woo,Lee, Seung Hwan,Cho, Young Jin,Yoon, Cheol Min
, p. 145 - 146 (2007/10/03)
Aldehydes and ketones were easily converted to the corresponding amines by the reaction of amines in methanol using decaborane (B10H14) at room temperature under nitrogen. The reaction is simple and efficient. The Royal Society of Chemistry 2000.
Formation of anilines from 5-nitro-2-phenylpyrimidine, amines, and acetone
Gromov, S. P.
, p. 1041 - 1043 (2007/10/02)
The reaction of 5-nitro-2-phenylpyrimidine with aliphatic amines and acetone gave N-substituted 4-nitroanilines.In addition, 2-methyl-5-nitropyridine was also obtained from ethylamine. - Key words: pyrimidine; transformation of cyclic intermediates; anilines; pyridine.
Nucleophilic Substitution of Aromatic Halides with Amines under High Pressure
Ibata, Toshikazu,Isogami, Yasushi,Toyoda, Jiro
, p. 1187 - 1190 (2007/10/02)
The reaction of aromatic chlorides, bromides and iodides with various primary or secondary amines in a tetrahydrofuran solution under high pressure of 6-12 kbar gave the corresponding secondary and tertiary aromatic amines. 1,4-Diazabicyclooctane and quinuclidine gave N-aryl quaternary ammonium halides in high yields in contrast to the low reactivity of acyclic tertiary amines.