作者:Laha, Radha M.、Aich, Shobhon、Sarkar, Ankan Kumar、Dutta, Tanmoy、Ghosh, Narendra Nath、Khamarui, Saikat、Maiti, Dilip K.
DOI:10.1039/d4ob01004c
日期:——
Azomethine ylides are generated using either organocatalysts or metal catalysts via a ballet of decarboxylative C–N coupling choreographed by prolines. These strategies enable diastereoselective [3 + 2] cycloaddition, C–C coupling, and ring annulation, providing sustainable routes. The synthesized pyrrolizines and other heterocycles have potential applications in the development of crucial biomolecules
甲亚胺叶立德是使用有机催化剂或金属催化剂,通过脯氨酸精心设计的脱羧 C-N 偶联生成的。这些策略可实现非对映选择性 [3 + 2] 环加成、C-C 偶联和环化,从而提供可持续的路线。合成的吡咯嗪和其他杂环化合物在关键生物分子和药物的开发中具有潜在的应用。偶氮甲碱叶立德的内选择性是通过 DFT 计算实现和支持的。