Guangdong Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China.
Org Lett. 2020 Jul 17;22(14):5600-5604. doi: 10.1021/acs.orglett.0c01957. Epub 2020 Jul 6.
A unique, rhodium-catalyzed reaction of cyclopropene carboxylic acids with isatins has been developed, which takes place through a trapping process of transient cyclic carboxylic oxonium ylides. This reaction tolerates a wide variety of cyclopropene carboxylic acids and -protected or unprotected isatins and represents a new, direct strategy to access valuable γ-substituted γ-butenolide architectures containing an oxindole moiety in very high yields under mild reaction conditions.
开发了一种独特的、铑催化的环丙烯羧酸与色满酮的反应,该反应通过瞬态环状羧酸氧翁离子的捕获过程进行。该反应能容忍各种环丙烯羧酸和保护的或未保护的色满酮,代表了一种新的、直接的策略,可在温和的反应条件下以非常高的收率获得含有吲哚部分的有价值的γ-取代γ-丁烯内酯结构。