作者:Dario Perdicchia
DOI:10.1016/j.tet.2023.133432
日期:2023.6
An efficient synthetic method of ionic hydrogenation of azine to the corresponding 1,2-dialkylhydrazines was accomplished. Reaction time was fast and isolation and purification of the 1,2-dialkylhydrazines were operationally simple. Yields were almost quantitative for most of the products with good functional group tolerance. Moreover, the byproduct of reduction gave the opportunity for the selective
实现了吖嗪离子氢化为相应的 1,2-二烷基肼的有效合成方法。反应时间快,1,2-二烷基肼的分离和纯化操作简单。大多数具有良好官能团耐受性的产品的产量几乎是定量的。此外,还原的副产物为单酰肼的原位选择性合成提供了机会,从而扩展了所述合成方法的潜力。