Karnbrock Simon B H, Golz Christopher, Alcarazo Manuel
Institute of Organic and Biomolecular Chemistry, University of Göttingen, Tammannstraße 2, 37077 Göttingen, Germany.
Chem Commun (Camb). 2024 Jun 27;60(53):6745-6748. doi: 10.1039/d4cc02202e.
The cooperation between a geometrically constrained, highly electrophilic phosphorus(V) center, and an electronically rich tetradentate bis(amidophenolate) ligand enables the cleavage of the CO bond from typical aldehydes and ketones delivering iminio phosphoramidate species. The amphiphilic nature of these products, which is demonstrated through their reaction with typical Lewis acids and bases, enables their use as a mild source of silylium cations from silanes, allowing the selective reductive coupling of aldehydes to ethers under catalytic conditions.
几何受限的、高亲电性的磷(V)中心与富电子的四齿双(酰胺基酚盐)配体之间的合作,能够从典型的醛和酮中裂解CO键,生成亚胺基磷酰胺物种。这些产物的两亲性通过它们与典型路易斯酸和碱的反应得以证明,这使得它们能够作为硅烷中亚硅阳离子的温和来源,从而在催化条件下实现醛到醚的选择性还原偶联。