N,N-bis(trimethylsilyl)methoxymethylamine as a convenient synthetic equivalent for +CH2NH2: N,N-bis(trimethylsilyl)aminomethylation of silyl sulphides and phosphites
作者:Toshiaki Morimoto、Masahiro Aono、Minoru Sekiya
DOI:10.1039/c39840001055
日期:——
N-Silyl-protected primary aminomethyl sulphides and aminomethylphosphonates can be synthesised by the Lewis acid-catalysed reactions of silyl sulphides and silylphosphites with N,N-bis(trimethylsilyl)methoxymethylamine.
A CONVENIENT SYNTHETIC METHOD FOR SCHIFF BASES. THE TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE-CATALYZED REACTION OF<i>N</i>,<i>N</i>-BIS(TRIMETHYLSILYL)AMINES WITH ALDEHYDES AND KETONES
作者:Toshiaki Morimoto、Minoru Sekiya
DOI:10.1246/cl.1985.1371
日期:1985.9.5
N,N-Bis (trimethylsilyl)amines react with aldehydes or ketones in the presence of trimethylsilyl trifluoromethanesulfonate to give Schiffbases in high yields. In situ utilization of the reaction solution as the Schiff base is also demonstrated.