作者:Ning Jiao、Cheng Zhang、Jianzhong Liu、Zengrui Cheng、Junhua Li、Song Song
DOI:10.1055/a-2006-4548
日期:——
The development of novel methods for the preparation of aminotetrazoles is of long-standing interest to chemists due to the great importance of these compounds in chemistry and biology. Here, we report an efficient method for the preparation of aminotetrazoles from secondary amides by selective C–C bond cleavage. Compared with the conventional laborious and cumbersome approaches to aminotetrazoles
由于这些化合物在化学和生物学中的重要性,开发用于制备氨基四唑的新方法一直是化学家的兴趣所在。在这里,我们报告了一种通过选择性 C-C 键断裂从仲酰胺制备氨基四唑的有效方法。与传统的费力和繁琐的氨基四唑方法相比,这种化学方法提供了一种高效的氮化策略,一步将四个氮原子安装到仲酰胺中。