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Jinqian Liu
Observed names:
JINQIAN LIU,
Jin-Qian Liu,
JinQian Liu,
Jin‐Qian Liu,
Liu, Jinqian
Institution:
Shaanxi Coal Chemical Industry Technology Research Institute
Observed institutions:
Amgen (United States),
East China University of Science and Technology,
Chinese Academy of Sciences,
Shanghai Institute of Materia Medica,
Shaanxi Coal Chemical Industry Technology Research Institute,
Wake Forest University,
University of Nebraska Medical Center
show all 7
ORCID:
0000-0002-8141-9588
Observed ORCID:
0000-0002-8141-9588
OpenAlex ID:
A5005645688
Sodium stearate-catalyzed multicomponent reactions for efficient synthesis of spirooxindoles in aqueous micellar media
2009
·
Li-Min Wang
, Ning Jiao
, et al.
·
Tetrahedron
·
208
AMG 837: A potent, orally bioavailable GPR40 agonist
2011
·
Jonathan B. Houze
, Liusheng Zhu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
134
SAR and Mode of Action of Novel Non-Nucleoside Inhibitors of Hepatitis C NS5b RNA Polymerase
2006
·
Jay P. Powers
, Derek E. Piper
, et al.
·
Journal of Medicinal Chemistry
·
132
Discovery and initial SAR of inhibitors of interleukin-1 receptor-associated kinase-4
2006
·
Jay P. Powers
, Shyun Li
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
123
Discovery of AM-1638: A Potent and Orally Bioavailable GPR40/FFA1 Full Agonist
2012
·
Sean P. Brown
, Paul J. Dransfield
, et al.
·
ACS Medicinal Chemistry Letters
·
93
Synthesis of tetraketones in water and under catalyst-free conditions
2009
·
Jian-Jun Yu
, Li-Min Wang
, et al.
·
Green Chemistry
·
90
Targeted Drug Delivery to Chemoresistant Cells: Folic Acid Derivatization of FdUMP[10] Enhances Cytotoxicity toward 5-FU-Resistant Human Colorectal Tumor Cells
2001
·
Jinqian Liu
, Carol Kolar
, et al.
·
The Journal of Organic Chemistry
·
75
Synthesis and optimization of substituted furo[2,3-d]-pyrimidin-4-amines and 7H-pyrrolo[2,3-d]pyrimidin-4-amines as ACK1 inhibitors
2012
·
XianYun Jiao
, David J. Kopecky
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
66
Metabolism of MRX-I, a Novel Antibacterial Oxazolidinone, in Humans: The Oxidative Ring Opening of 2,3-Dihydropyridin-4-One Catalyzed by Non-P450 Enzymes
2015
·
Jian Meng
, Dafang Zhong
, et al.
·
Drug Metabolism and Disposition
·
56
A Concise Domino Synthesis of Benzo‐1,4‐heterocycle Compounds via a Piancatelli/C–N Coupling/Michael Addition Process Promoted by La(OTf)3
2012
·
Jinqian Liu
, Qiang Shen
, et al.
·
European Journal of Organic Chemistry
·
40
AlCl3-Promoted Formal [2 + 3]-Cycloaddition of 1,1-Cyclopropane Diesters with N-Benzylic Sulfonamides To Construct Highly Stereoselective Indane Derivatives
2014
·
Mengyun Zhu
, Jinqian Liu
, et al.
·
Organic Letters
·
36
Discovery and optimization of a novel series of GPR142 agonists for the treatment of type 2 diabetes mellitus
2012
·
Mike Lizarzaburu
, Simon Turcotte
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
36
Nonclinical Evaluation of Antibacterial Oxazolidinones Contezolid and Contezolid Acefosamil with Low Serotonergic Neurotoxicity
2021
·
Wen Wang
, Kate M. Voss
, et al.
·
Chemical Research in Toxicology
·
33
Increased Cytotoxicity and Decreased In Vivo Toxicity of FdUMP[10] Relative to 5-FU
1999
·
Jinqian Liu
, Alan Skradis
, et al.
·
Nucleosides and Nucleotides
·
26
Insights into the Distinct Behaviors between Bifunctional and Binary Organoborane Catalysts through Terpolymerization of Epoxide, CO2, and Anhydride
2024
·
Rui Xie
, Yuhui Wang
, et al.
·
Angewandte Chemie International Edition
·
22
PDF
Design and Synthesis of Protein Superfamily-Targeted Chemical Libraries for Lead Identification and Optimization
2005
·
Stephen Shuttleworth
, Richard Connors
, et al.
·
Current Medicinal Chemistry
·
22
Discovery of the imidazole-derived GPR40 agonist AM-3189
2015
·
Zhihua Ma
, Daniel C.-H. Lin
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
21
Positive Interaction between 5-FU and FdUMP[10] in the Inhibition of Human Colorectal Tumor Cell Proliferation
1999
·
JINQIAN LIU
, JEFF KOLATH
, et al.
·
Antisense and Nucleic Acid Drug Development
·
21
Discovery of Antibacterial Contezolid Acefosamil: Innovative O-Acyl Phosphoramidate Prodrug for IV and Oral Therapies
2022
·
Jinqian Liu
, Wen Wang
, et al.
·
ACS Medicinal Chemistry Letters
·
19
Nickel‐Catalyzed One‐Pot Suzuki–Miyaura Cross‐Coupling of Phenols and Arylboronic Acids Mediated by N,N‐Ditosylaniline
2014
·
Liangshun Chen
, Hongyue Lang
, et al.
·
European Journal of Organic Chemistry
·
18
Novel Role of p-Toluenesulfonamide in the Preparation of 4,5-Diaminocyclopent-2-enones
2013
·
Jianjun Yu
, Limin Wang
, et al.
·
Synthesis
·
18
Yb(OTf)3-promoted effective benzylation and allylation with N-tosyl amino group as a stable leaving group
2012
·
Jinqian Liu
, Limin Wang
, et al.
·
Tetrahedron Letters
·
16
Efficacy and safety of FdUMP[10] in treatment of HT-29 human colon cancer xenografts
2002
·
Changnian Liu
, Mark Willingham
, et al.
·
International Journal of Oncology
·
14
Cytotoxicity and In Vivo Tolerance of FdUMP[10]: A Novel Pro-Drug of the TS Inhibitory Nucleotide FdUMP
1999
·
William H. Gmeiner
, Alan Skradis
, et al.
·
Nucleosides and Nucleotides
·
12
Solvent-Free Amination of Secondary Benzylic Alcohols with N-Nucleophiles Catalyzed by FeCl3
2011
·
Jian-Jun Yu
, Li-Min Wang
, et al.
·
Synthetic Communications
·
11
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Works count:
39
Citation count:
1,367
H-index:
19
I10-index:
26
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