Abstract In recent years β-phosphoryl ketones were considered as valuable intermediates in organic synthesis. In the present work we studied the reaction of enamines 1 with monochlorophosphine 2 which led to the β-phosphinoyl cycloalkanones 3. The structure of products 3 was confirmed by NMR and IR spectroscopy.
摘要 近年来,β-
磷酰基酮被认为是有机合成中有价值的中间体。在目前的工作中,我们研究了烯胺 1 与一
氯膦 2 的反应,这导致了 β-膦酰基环烷酮 3。产物 3 的结构由核磁共振和红外光谱证实。