TiCl4induced N-Methyleneamine Equivalents: A New Route to Aminoacetonitriles
摘要:
TiCl4 induced N-methyleneamine equivalents from hexahydro-1,3,5-triazines or N-(methoxymethyl)amines were reacted with trimethylsilyl cyanide to give aminoacetonitriles in 40-90% yield.
HA, HYUN-JOON;NAM, GONG-SIL;PARK, KYONG PAE, SYNTH. COMMUN., 21,(1991) N, C. 155-160
作者:HA, HYUN-JOON、NAM, GONG-SIL、PARK, KYONG PAE
DOI:——
日期:——
TiCl<sub>4</sub>induced N-Methyleneamine Equivalents: A New Route to Aminoacetonitriles
作者:Hyun-Joon Ha、Gong-Sil Nam、Kyong Pae Park
DOI:10.1080/00397919108020806
日期:1991.1
TiCl4 induced N-methyleneamine equivalents from hexahydro-1,3,5-triazines or N-(methoxymethyl)amines were reacted with trimethylsilyl cyanide to give aminoacetonitriles in 40-90% yield.