Site-Selective γ-C(sp<sup>3</sup>)−H and γ-C(sp<sup>2</sup>)−H Arylation of Free Amino Esters Promoted by a Catalytic Transient Directing Group
作者:Hua Lin、Chao Wang、Thomas D. Bannister、Theodore M. Kamenecka
DOI:10.1002/chem.201802465
日期:2018.7.5
The first selective PdII‐catalysed γ‐C(sp3)−H and γ‐C(sp2)−H arylation of free amino esters using a commercially available catalytic transient directing group. A variety of free amino esters, including α‐amino esters and β‐amino esters, amino monoesters and amino bis‐esters, are shown to react with a diverse range of simple aryl and heteroaryl iodide reagents.
[EN] NOVEL POTASSIUM CHANNEL INHIBITORS<br/>[FR] NOUVEAUX INHIBITEURS DU CANAL POTASSIQUE
申请人:ACECION PHARMA APS
公开号:WO2022200162A1
公开(公告)日:2022-09-29
The present invention relates to a compound of the general formula (I). The compounds of formula I are useful for treatment of a cardiac disease, disorder or condition in a mammal.