Yuanxiang Wang

发表

A Thiol-Ene Coupling Approach to Native Peptide Stapling and Macrocyclization.

D. Chou, Yuanxiang Wang, 2015, Angewandte Chemie.

Selective N-terminal functionalization of native peptides and proteins† †Electronic supplementary information (ESI) available: Experimental details. See DOI: 10.1039/c6sc04744k Click here for additional data file.

D. Chou, Yuanxiang Wang, Diao Chen, 2017, Chemical science.

An expeditious approach to access 2-arylimidazo[1,2-a]pyridin-3-ol from 2-amino pyridine through a novel Petasis based cascade reaction

Hong‐yu Li, B. Saha, Yuanxiang Wang, 2014 .

A p-toluenesulfinic acid-catalyzed three-component Ugi-type reaction and its application for the synthesis of α-amino amides and amidines

Hong‐yu Li, B. Saha, Yuanxiang Wang, 2013 .

Targeting the K‐Ras/PDEδ Protein–Protein Interaction: The Solution for Ras‐Driven Cancers or Just Another Therapeutic Mirage?

Hong‐yu Li, Yuanxiang Wang, B. Frett, 2013, ChemMedChem.

Application of Thiol-yne/Thiol-ene Reactions for Peptide and Protein Macrocyclizations.

T. Cheatham, Carol S. Lim, B. Bruno, 2017, Chemistry.

D. Chou, Yuanxiang Wang, Diao Chen, 2017, Chemical science.

One-Pot Three-Step Synthesis of Naphtho[2,3-a]carbazole- 5,13-diones using a Tandem Radical Alkylation–Cyclization– Aromatization Reaction Sequence

Yuanxiang Wang, W. Hu, Qizheng Yao, 2010 .

Identification of pyrazine-based TrkA inhibitors: design, synthesis, evaluation, and computational modeling studies.

Zhigang Xu, Hong‐yu Li, Yuanxiang Wang, 2014, MedChemComm.

In Vitro Pharmacokinetic Optimizations of AM2-S31N Channel Blockers Led to the Discovery of Slow-Binding Inhibitors with Potent Antiviral Activity against Drug-Resistant Influenza A Viruses.

Chunlong Ma, Jun Wang, Yanmei Hu, 2018, Journal of medicinal chemistry.

Structure-Property Relationship Studies of Influenza A Virus AM2-S31N Proton Channel Blockers.

Chunlong Ma, Jun Wang, Yanmei Hu, 2018, ACS medicinal chemistry letters.

Poly(4-ketovalerolactone) from Levulinic acid: Synthesis and Hydrolytic Degradation.

T. Hoye, Yuanxiang Wang, Shu Xu, 2020, Macromolecules.

Synthesis and c-Met kinase inhibition of 3,5-disubstituted and 3,5,7-trisubstituted quinolines: identification of 3-(4-acetylpiperazin-1-yl)-5-(3-nitrobenzylamino)-7- (trifluoromethyl)quinoline as a novel anticancer agent.

Yi Chen, M. Geng, Gang Liu, 2011, Journal of medicinal chemistry.

Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed Three-Component Reaction under Microwave Irradiation

Hong‐yu Li, Yuanxiang Wang, B. Frett, 2014, Organic letters.

Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: key precursors to potent c-Met inhibitors.

M. Geng, Gang Liu, Yuanxiang Wang, 2011, Organic & biomolecular chemistry.

Computer aided drug discovery of highly ligand efficient, low molecular weight imidazopyridine analogs as FLT3 inhibitors.

Catherine C. Smith, N. Shah, Hong‐yu Li, 2015, European journal of medicinal chemistry.

Metal-free, efficient hydrazination of imidazo[1,2-a]pyridine with diethyl azodicarboxylate in neutral media.

Hong‐yu Li, Yuanxiang Wang, B. Frett, 2015, Organic & biomolecular chemistry.

Intramolecular Capture of HDDA-Derived Benzynes: (i) 6- to 12-Membered Ring Formation, (ii) Internally (vis-à-vis Remotely) Tethered Traps, and (iii) Role of the Rate of Trapping by the Benzynophile.

T. Hoye, Yuanxiang Wang, 2018, Organic letters.

A p‐Toluenesulfinic Acid Catalyzed Three‐Component Ugi‐Type Reaction and Its Application for the Synthesis of α‐Amino Amides and Amidines.

B. Saha, Yuanxiang Wang, B. Frett, 2013 .

Multisubstituted quinoxalines and pyrido[2,3-d]pyrimidines: synthesis and SAR study as tyrosine kinase c-Met inhibitors.

Yechun Xu, M. Geng, Qiu-feng Liu, 2012, Bioorganic & medicinal chemistry letters.

Metal- and additive-free direct C3-aminomethylation of imidazo[1,2-a]pyridines with 1,3,5-triazinanes

Zhimin Jiang, Yuanxiang Wang, Zongbo Feng, 2022, Tetrahedron Letters.

Poly(α-methyleneglutarimide)s from radical polymerization of α-methyleneglutarimides

T. Hoye, Yuanxiang Wang, Shu Xu, 2018 .

Discovery of novel c-Met kinase inhibitors bearing a thieno[2,3-d]pyrimidine or furo[2,3-d]pyrimidine scaffold.

Yi Chen, M. Geng, Yuanxiang Wang, 2011, Bioorganic & medicinal chemistry.

Targeting mutant KRAS for anticancer therapeutics: a review of novel small molecule modulators.

Hong‐yu Li, Yuanxiang Wang, B. Frett, 2013, Journal of medicinal chemistry.

Design and expeditious synthesis of organosilanes as potent antivirals targeting multidrug-resistant influenza A viruses.

Chunlong Ma, Jun Wang, Yanmei Hu, 2017, European journal of medicinal chemistry.

Sulfonamide-Trapping Reactions of Thermally Generated Benzynes.

T. Hoye, Yuanxiang Wang, Lianyou Zheng, 2018, Organic letters.

Expeditious synthesis of 2,3-dihydro-2-alkoxy-3-methylenebenzofurans from N-benzofuran-3-ylmethyl N,N,N-trialkylammonium bromides: a new approach to access the natural product, 2-hydroxy-3-methylene-6-methyl-2, 3-dihydrobenzofuran

Yuanxiang Wang, A. Zhang, 2009 .

Synthesis study on marmycin A: preparation of the C3'-desmethyl analogues.

Linghua Meng, Yuanxiang Wang, W. Hu, 2009, The Journal of organic chemistry.

Discovery of Potent Antivirals against Amantadine-Resistant Influenza A Viruses by Targeting the M2-S31N Proton Channel.

Chunlong Ma, Jun Wang, Yanmei Hu, 2016, ACS infectious diseases.

Expeditious Lead Optimization of Isoxazole-Containing Influenza A Virus M2-S31N Inhibitors Using the Suzuki-Miyaura Cross-Coupling Reaction.

Chunlong Ma, Jun Wang, Yanmei Hu, 2017, Journal of medicinal chemistry.

Exploring Ugi-Azide Four-Component Reaction Products for Broad-Spectrum Influenza Antivirals with a High Genetic Barrier to Drug Resistance

C. Hulme, Chunlong Ma, Jun Wang, 2018, Scientific Reports.

Further SAR studies on 3,5-diamino-7-trifluoromethylquinolines as highly potent tyrosine kinase c-Met inhibitors: efforts to correct hERG inhibition

Yi Chen, M. Geng, Zhaobing Gao, 2012 .

Isomerizations of Propargyl 3-Acylpropiolates via Reactive Allenes.

T. Hoye, Yuanxiang Wang, 2018, Organic letters.

Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: key precursors to potent c-Met inhibitors.

M. Geng, Gang Liu, Yuanxiang Wang, 2011, Organic & biomolecular chemistry.

Selective N-terminal functionalization of native peptides and proteins

D. Chou, Yuanxiang Wang, Diao Chen, 2017, Chemical science.