艾伦
金属转移
炔丙基
催化作用
化学
钯
芳基
产量(工程)
组合化学
锂(药物)
选择性
表面改性
有机化学
材料科学
医学
烷基
物理化学
冶金
内分泌学
作者
Jaime Mateos,Anirban Mondal,Marta Castiñeira Reis,Ben L. Feringa
标识
DOI:10.1002/anie.201913132
摘要
Abstract A palladium‐catalyzed cross‐coupling between in situ generated allenyl/propargyl‐lithium species and aryl bromides to yield highly functionalized allenes is reported. The direct and selective formation of allenic products preventing the corresponding isomeric propargylic product is accomplished by the choice of SPhos or XPhos based Pd catalysts. The methodology avoids the prior transmetalation to other transition metals or reverse approaches that required prefunctionalization of substrates with leaving groups, resulting in a fast and efficient approach for the synthesis of tri‐ and tetrasubstituted allenes. Experimental and theoretical studies on the mechanism show catalyst control of selectivity in this allene formation.
科研通智能强力驱动
Strongly Powered by AbleSci AI