Palladium-Catalyzed C6-Selective C–H Acylation of 2-Pyridones
Author:
Affiliation:
1. College of Pharmaceutical Sciences, Zhejiang University of Technology
2. Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology
Abstract
Funder
National Natural Science Foundation of China
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0040-1706546.pdf
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2. MK-0536 Inhibits HIV-1 Integrases Resistant to Raltegravir
3. The first total synthesis of potent human chymase inhibitor SPF32629B via regioselective bromination and O-acylation strategy
4. Cross-Coupling of α-Carbonyl Sulfoxonium Ylides with C−H Bonds
5. Ru(ii)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
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1. Directing group-assisted selective C–H activation of six-membered N-heterocycles and benzo-fused N-heterocycles;Organic Chemistry Frontiers;2024
2. Transition Metal‐Catalyzed CH Functionalization of Aldehydes;Handbook of CH‐Functionalization;2022-11-29
3. Recent Advances in Palladium‐Based Cross‐Dehydrogenative‐Coupling (CDC) with C(sp 2 )H/C(sp 2 )H Bond to Form New C(sp 2 )C(sp 2 ) Bond;Handbook of CH‐Functionalization;2022-11-29
4. Rh(III)‐Catalyzed C6‐Selective C−H 3‐Oxoalkylation of 2‐Pyridones with Allylic Alcohols;Asian Journal of Organic Chemistry;2022-07-09
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