Friis Stig D, Pirnot Michael T, Buchwald Stephen L
Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
J Am Chem Soc. 2016 Jul 13;138(27):8372-5. doi: 10.1021/jacs.6b04566. Epub 2016 Jul 1.
Detailed in this Communication is the enantioselective synthesis of 1,1-diarylalkanes, a structure found in a range of pharmaceutical drug agents and natural products, through the employment of copper(I) hydride and palladium catalysis. Judicious choice of ligand for both Cu and Pd enabled this hydroarylation protocol to work for an extensive array of aryl bromides and styrenes, including β-substituted vinylarenes and six-membered heterocycles, under relatively mild conditions.
本通讯详细介绍了通过使用氢化亚铜和钯催化对1,1-二芳基烷烃进行对映选择性合成,1,1-二芳基烷烃是在一系列药物制剂和天然产物中发现的一种结构。对铜和钯的配体进行明智选择,使得这种氢芳基化反应方案能够在相对温和的条件下,适用于多种芳基溴化物和苯乙烯,包括β-取代的乙烯基芳烃和六元杂环。