Qing Huang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Qing Huang has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Liangxian Liu
Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, P. R. China
3 shared publications - Haiping He
Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases of Ministry of Education, School of Pharmaceutical Science of Gannan Medical University, Ganzhou 341000, China
2 shared publications - Xiangjun Peng
Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases of Ministry of Education
2 shared publications - Fan Li
Key Laboratory of Organo-pharmaceutical Chemistry of Jiangxi Province, Gannan Normal University, Ganzhou 341000, China
1 shared publication - Hong Li
Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou 341000, China
1 shared publication - Jian Hu
Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Ministry of Education, Gannan Medical University, Ganzhou 341000, China
1 shared publication
Latest Publications
- Open Access
Visible-Light-Induced, Graphene Oxide-Promoted C3-Chalcogenylation of Indoles Strategy under Transition-Metal-Free Conditions
An efficient and general method for the synthesis of 3-sulfenylindoles and 3-selenylindoles employing visible-light irradiation with graphene oxide as a promoter at room temperature has been achieved. The reaction features are high yields, simple operation, metal-free and iodine-free conditions, an easy-to-handle oxidant, and gram-scalable synthesis. This simple protocol allows one to access a wide range of 3-arylthioindoles, 3-arylselenylindoles, and even 3-thiocyanatoindoles with good to excellent yields.
Open AccessVisible-Light-Induced, Graphene Oxide-Promoted C3-Chalcogenylation of Indoles Strategy under Transition-Metal-Free Conditions
An efficient and general method for the synthesis of 3-sulfenylindoles and 3-selenylindoles employing visible-light irradiation with graphene oxide as a promoter at room temperature has been achieved. The reaction features are high yields, simple operation, metal-free and iodine-free conditions, an easy-to-handle oxidant, and gram-scalable synthesis. This simple protocol allows one to access a wide range of 3-arylthioindoles, 3-arylselenylindoles, and even 3-thiocyanatoindoles with good to excellent yields.
- Open Access
Photoinitiated Multicomponent Anti-Markovnikov Alkoxylation over Graphene Oxide
The development of graphene oxide–based heterogeneous materials with an economical and environmentally–friendly manner has the potential to facilitate many important organic transformations but proves to have few relevant reported reactions. Herein, we explore the synergistic role of catalytic systems driven by graphene oxide and visible light that form nucleophilic alkoxyl radical intermediates, which enable an anti-Markovnikov addition exclusively to the terminal alkenes, and then the produced benzyl radicals are subsequently added with N–methylquinoxalones. This photoinduced cascade radical difunctionalization of olefins offers a concise and applicable protocol for constructing alkoxyl–substituted N–methylquinoxalones.
Open AccessPhotoinitiated Multicomponent Anti-Markovnikov Alkoxylation over Graphene Oxide
The development of graphene oxide–based heterogeneous materials with an economical and environmentally–friendly manner has the potential to facilitate many important organic transformations but proves to have few relevant reported reactions. Herein, we explore the synergistic role of catalytic systems driven by graphene oxide and visible light that form nucleophilic alkoxyl radical intermediates, which enable an anti-Markovnikov addition exclusively to the terminal alkenes, and then the produced benzyl radicals are subsequently added with N–methylquinoxalones. This photoinduced cascade radical difunctionalization of olefins offers a concise and applicable protocol for constructing alkoxyl–substituted N–methylquinoxalones.
- 13 February 2017
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 28 (09) , 1087-1090
Multicomponent Cascade Synthesis of 1,4-Dihydropyridine Derivatives from Pyridines, Methyl Propiolate, and Aromatic Acids
A metal-free highly efficient synthesis of a wide range of 4-propenyl 1,4-DHPs from pyridines, methyl propiolate, and aromatic acids is described. The reactions are conducted under convenient conditions and provide products with excellent regioselectivity in good to excellent yields, with broad substrate scope.
- 13 February 2017
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 28 (09) , 1087-1090
Multicomponent Cascade Synthesis of 1,4-Dihydropyridine Derivatives from Pyridines, Methyl Propiolate, and Aromatic Acids
A metal-free highly efficient synthesis of a wide range of 4-propenyl 1,4-DHPs from pyridines, methyl propiolate, and aromatic acids is described. The reactions are conducted under convenient conditions and provide products with excellent regioselectivity in good to excellent yields, with broad substrate scope.