当前位置: X-MOL 学术Chem. Commun. › 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.)
Direct C–H alkylation of 3,4-dihydroquinoxaline-2-ones with N-(acyloxy)phthalimides via radical–radical cross coupling
Chemical Communications ( IF 4.9 ) Pub Date : 2024-05-23 , DOI: 10.1039/d4cc01837k
Sudhir Kumar Hota 1 , Gulshan Singh 1 , Sandip Murarka 1
Affiliation  

We present an organophotoredox-catalyzed direct Csp3–H alkylation of 3,4-dihydroquinoxalin-2-ones employing N-(acyloxy)pthalimides to provide corresponding products in good yields. A broad spectrum of NHPI esters (1°, 2°, 3°, and sterically encumbered) participates in the photoinduced alkylation of a variety of 3,4-dihydroquinoxalin-2-ones. In general, mild conditions, broad scope with good functional group tolerance, and scalability are the salient features of this direct alkylation process.

中文翻译:


3,4-二氢喹喔啉-2-酮与N-(酰氧基)邻苯二甲酰亚胺通过自由基-自由基交叉偶联直接C-H烷基化



我们提出了一种有机光氧化还原催化的 3,4-二氢喹喔啉-2-酮的直接 Csp 3 -H 烷基化反应,使用 N-(酰氧基)邻苯二甲酰亚胺,以良好的产率提供相应的产物。多种 NHPI 酯(1°、2°、3° 和空间阻碍)参与多种 3,4-二氢喹喔啉-2-酮的光诱导烷基化。总体而言,该直接烷基化工艺的显着特点是条件温和、适用范围广、官能团耐受性好、可扩展性好。
更新日期:2024-05-23
down
wechat
bug