Shanghai Key Laboratory of New Drug Design & School of Pharmacy, East China University of Science and Technology , 130 Meilong Road, Shanghai 200237, China.
Org Lett. 2017 Sep 1;19(17):4520-4523. doi: 10.1021/acs.orglett.7b02096. Epub 2017 Aug 24.
A novel protocol for the synthesis of unsymmetrical indigo-like (E)-α-amino enaminones by rhodium-catalyzed transformations of isatins with 1-tosyl-1,2,3-triazoles has been developed. A plausible reaction mechanism is proposed to account for the formation of structurally important unsymmetrical indigo analogues, which represents a new strategy for C-C bond formation based on the transformations of secondary amides and rhodium azavinylcarbenes.
发展了一种通过铑催化靛红与 1-对甲苯磺酰基-1,2,3-三唑的转化合成不对称靛蓝样(E)-α-氨基烯胺酮的新方法。提出了一个合理的反应机制来解释结构重要的不对称靛蓝类似物的形成,这代表了一种基于仲酰胺和铑氮烯基卡宾转化的新的 C-C 键形成策略。