Generation of 1-Azapentadienyl Anion from N-(tert-Butyldimethylsilyl)-3-buten-1-amine
摘要:
N-(tert-Butyldimethylsilyl)-3-buten-1-amine undergoes allylic deprotonation at the 2-position when exposed to 2 equiv of nBuLi in THE This allylic anion undergoes lithium hydride elimination to generate a 1-azapentadienyl anion. The anion is generated cleanly and completely.
Generation of 1-Azapentadienyl Anion from N-(tert-Butyldimethylsilyl)-3-buten-1-amine
摘要:
N-(tert-Butyldimethylsilyl)-3-buten-1-amine undergoes allylic deprotonation at the 2-position when exposed to 2 equiv of nBuLi in THE This allylic anion undergoes lithium hydride elimination to generate a 1-azapentadienyl anion. The anion is generated cleanly and completely.
Generation of 1-Azapentadienyl Anion from <i>N</i>-(<i>tert</i>-Butyldimethylsilyl)-3-buten-1-amine
作者:Madeleine A. Jacobson、Paul G. Williard
DOI:10.1021/jo0162336
日期:2002.5.1
N-(tert-Butyldimethylsilyl)-3-buten-1-amine undergoes allylic deprotonation at the 2-position when exposed to 2 equiv of nBuLi in THE This allylic anion undergoes lithium hydride elimination to generate a 1-azapentadienyl anion. The anion is generated cleanly and completely.