H
Hong Liu
Researcher at Shandong University
Publications - 2349
Citations - 79103
Hong Liu is an academic researcher from Shandong University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 100, co-authored 1905 publications receiving 57561 citations. Previous affiliations of Hong Liu include Shanghai University & Guangzhou University.
Papers
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Journal ArticleDOI
Ru(II)-catalyzed C6-selective C–H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors
Yangjie Fu,Yangjie Fu,Zhaohui Wang,Zhaohui Wang,Qiyu Zhang,Qiyu Zhang,Zhiyu Li,Hong Liu,Hong Liu,Xiaoling Bi,Jiang Wang +10 more
TL;DR: A method using sulfoxonium ylides as carbene precursors to achieve C6-selective acylmethylation of pyridones catalyzed by a ruthenium(ii) complex offers a direct and efficient way to synthesize pyridine derivatives.
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Preparation of filled skutterudite nanowire by a hydrothermal method
Hong Liu,Hong Liu,Jiyang Wang,Xiaobo Hu,Lixia Li,Feng Gu,Shanrong Zhao,Mingyuan Gu,Robert I. Boughton,Minhua Jiang +9 more
TL;DR: In this paper, filled skutterudite NaFe 4 P 12 single crystalline nanowires were synthesized hydrothermally by the reaction of iron chloride, sodium hydroxide and white phosphorus at 160-180°C.
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Anisotropic thermal expansion of BiB3O6
Bing Teng,Zhengping Wang,Huaidong Jiang,Xiufeng Cheng,Hong Liu,Xiaobo Hu,Shengming Dong,Jiyang Wang,Zongshu Shao +8 more
TL;DR: In this paper, the anisotropic thermal expansion of BiB3O6 (BIBO) has been studied in the temperature range 25°C to 299.5°C.
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A novel aptameric biosensor based on the self-assembled DNA-WS2 nanosheet architecture.
TL;DR: This strategy was generalized to detect Hg2+ using a mercury-specific aptamer (MSO) and can be expected to offer a promising approach for designing high-performance electrochemical aptasensors for a spectrum of targets.
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PH006, a novel and selective Src kinase inhibitor, suppresses human breast cancer growth and metastasis in vitro and in vivo
Jingui Ma,He Huang,Si-meng Chen,Yi Chen,Xianliang Xin,Liping Lin,Jian Ding,Hong Liu,Linghua Meng +8 more
TL;DR: PH006 is a novel selective inhibitor of c-Src and possesses potent activity against breast cancer growth and metastasis, which could be potentially developed as a lead candidate against breast cancers with elevated Src tyrosine kinase activity.