当前位置: X-MOL 学术Org. Chem. Front. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Switching from gem-difluorovinylation to carboxylation: ligand-enabled palladium-catalyzed Heck annulation of alkene-tethered aryl halides with sodium difluorochloroacetate
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2024-04-30 , DOI: 10.1039/d4qo00392f
Yu Xia 1 , Wenqi Li 1 , Minzhu Wei 1 , Yonghong Zhang 1 , Bin Wang 1 , Shaofeng Wu 1 , Chenjiang Liu 1
Affiliation  

Reported herein is the use of a ligand to tune palladium-catalyzed intramolecular Heck gem-difluorovinylation and carboxylation with alkene-tethered aryl halides, which provides an efficient avenue for building indolo[2,1-a]isoquinoline skeletons. Sodium difluorochloroacetate (ClCF2COONa) acts as both a difluorocarbene (:CF2) and carboxyl source. A broad substrate scope, diversified transformations and gram scale-up reaction meant that the products had potential for their own further applications.

中文翻译:

从偕二氟乙烯基化转变为羧化:配体钯催化的烯烃束缚芳基卤化物与二氟氯乙酸钠的 Heck 环化

本文报道了使用配体来调节钯催化的Heck gem-二氟乙烯基化和与烯烃束缚的芳基卤化物的羧化,这为构建吲哚并[2,1- a ]异喹啉骨架提供了有效的途径。二氟氯乙酸钠 (ClCF 2 COONa) 既充当二氟卡宾 (:CF 2 ) 又充当羧基源。广泛的底物范围、多样化的转化和克级放大反应意味着该产品具有进一步应用的潜力。
更新日期:2024-04-30
down
wechat
bug