Zheng Jianxia, Darcel Christophe, Sortais Jean-Baptiste
UMR 6226 CNRS-Université Rennes 1, Institut des Sciences Chimiques de Rennes, Team Organometallics: Materials and Catalysis, Centre for Catalysis and Green Chemistry Campus de Beaulieu, 263 av. du Général Leclerc, 35042 Rennes Cedex, France.
Chem Commun (Camb). 2014 Nov 25;50(91):14229-32. doi: 10.1039/c4cc05517a.
Methylation of secondary amines was achieved using dimethyl carbonate or diethyl carbonate as the C1 source under the catalysis of well-defined half-sandwich iron complexes bearing an N-heterocyclic carbene ligand. The reaction proceeded under mild conditions in the presence of hydrosilanes as the reductants, and the amines were obtained with good to excellent isolated yields.
在带有N-杂环卡宾配体的明确界定的半夹心铁配合物催化下,使用碳酸二甲酯或碳酸二乙酯作为C1源实现了仲胺的甲基化。该反应在温和条件下,在硅烷作为还原剂存在的情况下进行,得到的胺的分离产率良好至优异。