State Key Laboratory of Chirosciences and Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University , Hung Hom, Kowloon, Hong Kong.
Org Lett. 2015 Sep 18;17(18):4612-5. doi: 10.1021/acs.orglett.5b02344. Epub 2015 Sep 9.
The rational design of a phosphine ligand for the reductive elimination-demanding Pd-catalyzed mono-α-arylation of acetone is demonstrated and reported. The catalyst is tolerant of previously proven challenging electron-deficient aryl chlorides and provides excellent product yields with down to 0.1 mol % Pd. Preliminary investigations suggest that the rate-limiting step for the proposed system is the oxidative addition of aryl chlorides, in which it contradicts previous findings regarding the α-arylation of acetone with aryl halides.
本文展示并报道了一种膦配体的合理设计,该配体可用于对还原消除要求较高的 Pd 催化丙酮单-α-芳基化反应。该催化剂可耐受先前已证明具有挑战性的缺电子芳基氯化物,并可在低至 0.1 mol % Pd 的用量下提供优异的产物收率。初步研究表明,所提出的体系的速率限制步骤是芳基氯化物的氧化加成,这与之前关于芳基卤化物与丙酮的α-芳基化反应的发现相矛盾。