Rh(iii)-catalyzed redox-neutral C–H activation/annulation of oxadiazolones with sulfoxonium ylides to access oxadiazoloisoquinolinone
化学
废止
催化作用
氧化还原
药物化学
组合化学
立体化学
有机化学
作者
Pothapragada S. K. Prabhakar Ganesh,Eswaran Kamaraj,Vairaperumal Veeramani,Rajaram Rajamohan,Perumal Muthuraja
出处
期刊：New Journal of Chemistry [Royal Society of Chemistry] 日期：2025-01-01卷期号：49 (12): 5093-5098被引量：2
标识
DOI：10.1039/d4nj05391e
摘要
Oxadiazolone-fused isoquinolines were synthesized via Rh( iii )-catalyzed [4+2] annulation and C–H activation, followed by acymethylation products with antidiabetic and anti-inflammatory potential.
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(2025-6-4)
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