College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, P.R. China.
Org Biomol Chem. 2019 Feb 20;17(8):2199-2203. doi: 10.1039/c8ob03057j.
A straightforward method for the synthesis of indolin-3-ones bearing a C2-quaternary functionality is reported. A series of 2,2-disubstituted indolin-3-ones were constructed in up to 94% yields in the absence of a metal catalyst. This cross-coupling reaction allows the facile synthesis of 2,2-disubstituted indolin-3-ones from readily available substrates in a short reaction time.
本文报道了一种合成具有 C2-季碳中心的吲唑-3-酮的简便方法。在没有金属催化剂的情况下,以高达 94%的收率构建了一系列 2,2-二取代的吲唑-3-酮。该交叉偶联反应允许从易得的底物中在短反应时间内轻松合成 2,2-二取代的吲唑-3-酮。