作者:Steven W. McDaniel、Charles M. Keyari、Kevin C. Rider、Nicholas R. Natale、Philippe Diaz
DOI:10.1016/j.tetlet.2011.08.096
日期:2011.10
A procedure for benzylic Suzuki–Miyaura cross-coupling under microwave conditions has been developed. These conditions allowed for heterocyclic compounds to be coupled. Optimum conditions found were Pd(OAc)2, JohnPhos as the catalyst and ligand, potassium carbonate as the base, and DMF as the solvent. Using these conditions, a library of structurally diverse compounds was synthesized.
已经开发了一种在微波条件下用于苄基 Suzuki-Miyaura 交叉偶联的程序。这些条件允许杂环化合物偶联。发现的最佳条件是 Pd(OAc) 2,JohnPhos 作为催化剂和配体,碳酸钾作为碱,DMF 作为溶剂。使用这些条件,合成了结构多样的化合物库。