W. Liu

发表

Branching cascades: a concise synthetic strategy targeting diverse and complex molecular frameworks.

Markus Schürmann, Wei Liu, V. Khedkar, 2011, Angewandte Chemie.

Reagent-controlled domino synthesis of skeletally-diverse compound collections.

Herbert Waldmann, Wei Liu, H. Waldmann, 2008, Chemical communications.

Cascade/domino synthesis strategy to enrich small molecule collections with skeletal diversity and molecular complexity

H. Waldmann, W. Liu, 2011 .

Discovery of an Orally Bioavailable Dual PI3K/mTOR Inhibitor Based on Sulfonyl-Substituted Morpholinopyrimidines.

Jiong Lan, Weiwei Wang, Liang Zhang, 2018, ACS medicinal chemistry letters.

1,1-Diarylalkenes as anticancer agents: dual inhibitors of tubulin polymerization and phosphodiesterase 4.

J. Leisten, Ling Zhang, Alexander L. Ruchelman, 2011, Bioorganic & medicinal chemistry.

The theoretical investigation of the binding mode between human serum albumin and penicillins

W. Liu, Weiren Xu, Fangyuan Shi, 2006 .

Systematic Structure-Activity Relationship (SAR) Exploration of Diarylmethane Backbone and Discovery of A Highly Potent Novel Uric Acid Transporter 1 (URAT1) Inhibitor

W. Liu, Weiren Xu, L. Tang, 2018, Molecules.

Discovery of novel tubulin inhibitors targeting the colchicine binding site via virtual screening, structural optimization and antitumor evaluation.

Hairui Jia, Shengzheng Wang, Guoqiang Dong, 2021, Bioorganic chemistry.

Nano-copper catalyzed three-component reaction to construct 1,4-substituted 1,2,3-triazoles

W. Liu, Congde Huo, Lina Huang, 2014 .

Synthesis and biological evaluation of pentanedioic acid derivatives as farnesyltransferase inhibitors

Honglin Li, Zhenjiang Zhao, Yufang Xu, 2015 .

Synthesis and cytotoxicity of 3-aryl acrylic amide derivatives of the simplified saframycin-ecteinascidin skeleton prepared from L-dopa.

W. Liu, Zhanzhu Liu, Wenfang Dong, 2013, European journal of medicinal chemistry.

Cu(OTf)2-Catalyzed 1,2,3-triazole-ring-controlled selective phenolic O–H bond methylthiomethylation

Yubo Jiang, W. Liu, Xinyuan Ma, 2019, Synthetic Communications.

Anemoside B4 sensitizes human colorectal cancer to fluorouracil-based chemotherapy through src-mediated cell apoptosis

W. Liu, X. He, Jun Tang, 2021, Aging.

Total synthesis and cytotoxicity of (−)-jorumycin and its analogues

W. Liu, Zhanzhu Liu, Wenfang Dong, 2012 .

Asymmetric synthesis and cytotoxicity of (-)-saframycin A analogues.

W. Liu, Zhanzhu Liu, Wenfang Dong, 2012, European journal of medicinal chemistry.

Asymmetric total synthesis of (-)-saframycin A from L-tyrosine.

W. Liu, Zhanzhu Liu, Shi-zhi Chen, 2011, The Journal of organic chemistry.

Total synthesis of (–)‐MY 336a from L‐tyrosine

W. Liu, Zhanzhu Liu, Wenfang Dong, 2009 .

Total synthesis of (−)-renieramycin G from l-tyrosine

W. Liu, S. Chen, Zhanzhu Liu, 2009 .

Branching cascades: a concise synthetic strategy targeting diverse and complex molecular frameworks.

V. Khedkar, M. Schürmann, Kamal Kumar, 2011, Angewandte Chemie.

Discovery of a Flexible Triazolylbutanoic Acid as a Highly Potent Uric Acid Transporter 1 (URAT1) Inhibitor

W. Liu, Weiren Xu, Zhixing Zhou, 2016, Molecules.

Novel carboline derivatives as potent antifungal lead compounds: design, synthesis, and biological evaluation.

Xiaomeng He, Shengzheng Wang, Jian Li, 2014, ACS medicinal chemistry letters.

Stereochemistry of microbiological hydroxylations of 1,4-cineole

J. J. Steffens, A. Goswami, F. Sariaslani, 1988 .

4,6-Dibromo-N-{3-[(4,6-dibromo-2,3-dimethylphenyl)imino]butan-2-ylidene}-2,3-dimethylaniline

W. Liu, Lina Huang, Zhengyin Du, 2013, Acta crystallographica. Section E, Structure reports online.

Metal-free selective aryl C–H formylation co-controlled by 1,2,3-triazole and hydroxyl using DMSO as formyl source

Yubo Jiang, W. Liu, Xinyuan Ma, 2019, Journal of Chemical Sciences.

Synthesis, structure and antibacterial activities of novel ferrocenyl-containing 1-phenyl-3-ferrocenyl-4-triazolyl-5-aryl-dihydropyrazole derivatives

W. Liu, Jianxin Fang, Zhong Jin, 2003 .

Discovery and in vitro evaluation of potent kinase inhibitors: Pyrido[1',2':1,5]pyrazolo[3,4-d]pyrimidines.

K. Lackey, Laurie S. Kane-Carson, E. Wood, 2005, Bioorganic & medicinal chemistry letters.

Preparation, characterization and biological activities of novel ferrocenyl‐substituted azaheterocycle compounds

W. Liu, Jianxin Fang, Zhong Jin, 2003 .

Nano‐Copper Catalyzed Three‐Component Reaction to Construct 1,4‐Substituted 1,2,3‐Triazoles.

W. Liu, Congde Huo, Lina Huang, 2014 .

Polyphosphoric Acid–Mediated, One-Pot, Novel Reactions to Build Polymethoxyarylnaphthalene Lignans

W. Liu, Weiren Xu, L. Tang, 2010 .

Synthesis and Biological Activity of 1 H -1,2,4-Triazole Alcohol Derivatives

H. Dai, W. Liu, Jianxin Fang, 2008 .

Synthesis and Fluoride Detection Properties of a Coumarin Derivative

Pingping Chen, Shuxiang Zhang, W. Liu, 2020, Russian Journal of Organic Chemistry.

Concise Synthesis and Antimicrobial Activities of New Substituted 5-Isoxazolpenicillins

Jiong Jia, W. Liu, Weiren Xu, 2007 .

Novel 4-amino-furo[2,3-d]pyrimidines as Tie-2 and VEGFR2 dual inhibitors.

Yutaka Maeda, Wei Liu, Megumi Shibahara, 2005, Bioorganic & medicinal chemistry letters.

Discovery of N-aryl-N'-pyrimidin-4-yl ureas as irreversible L858R/T790M mutant selective epidermal growth factor receptor inhibitors.

Y. Hu, Jiong Lan, Liang Zhang, 2017, Bioorganic & medicinal chemistry letters.

Design of SGLT2 Inhibitors for the Treatment of Type 2 Diabetes: A History Driven by Biology to Chemistry.

W. Liu, Linlin Jiang, Guilong Zhao, 2015, Medicinal chemistry (Shariqah (United Arab Emirates)).

Total synthesis of isoprekinamycin: structural evidence for enhanced diazonium ion character and growth inhibitory activity toward cancer cells.

N. Taylor, Matthew R. Buck, W. Liu, 2007, Organic letters.

Synthesis, characterization and bioactivity determination of ferrocenyl urea derivatives

W. Liu, D. Dong, Guo-Wei Yu, 2012 .

Protein Degradation via CRL4CRBN Ubiquitin Ligase: Discovery and Structure-Activity Relationships of Novel Glutarimide Analogs That Promote Degradation of Aiolos and/or GSPT1.

Chin-Chun Lu, L. LeBrun, Alexander L. Ruchelman, 2017, Journal of medicinal chemistry.

Synthesis of an isomer of the renieramycin skeleton from L‐tyrosine

W. Liu, Zhanzhu Liu, Wenfang Dong, 2011 .

Synthesis of an Isomer of the Renieramycin Skeleton from L-Tyrosine.

W. Liu, Zhanzhu Liu, Wenfang Dong, 2011 .

Synthesis and Molecular Recognition Properties of a Coumarin Derivative

Shuxiang Zhang, W. Liu, Pingping Chen, 2020, Journal of Physics: Conference Series.

Thiadiazole‐based Thioglycosides as Sodium‐glucose Co‐transporter 2 (SGLT2) Inhibitors

W. Liu, Weiren Xu, Yun Gao, 2010 .

Design, synthesis and biological activity of tetrazole-bearing uric acid transporter 1 inhibitors

W. Liu, Weiren Xu, L. Tang, 2017, Chemical Research in Chinese Universities.

3-Oxodapagliflozin as a potent and highly selective SGLT2 inhibitor for the treatment of type 2 diabetes

W. Liu, Weiren Xu, L. Tang, 2014, Chemical Research in Chinese Universities.

gem‐Dimethyl‐bearing C‐Glucosides as Sodium‐glucose Co‐transporter 2 (SGLT2) Inhibitors

W. Liu, Weiren Xu, Lida Tang, 2011 .

Novel carboline derivatives as potent antifungal lead compounds: design, synthesis, and biological evaluation.

Shengzheng Wang, Jian Li, Yongqiang Zhang, 2014, ACS Medicinal Chemistry Letters.

Discovery of Benzylidene Derivatives as Potent Syk Inhibitors: Synthesis, SAR Analysis, and Biological Evaluation

Hualiang Jiang, Jian Li, L. Miao, 2015, Archiv der Pharmazie.