Jiqing Jiang

发表

Aromatic nucleophilic substitution or CuI-catalyzed coupling route to martinellic acid.

D. Ma, C. Xia, Jiqing Jiang, 2003, The Journal of organic chemistry.

First Total Synthesis of Martinellic Acid, a Naturally Occurring Bradykinin Receptor Antagonist.

D. Ma, C. Xia, Jiqing Jiang, 2001 .

Incorporation of glucose analogs by GtfE and GtfD from the vancomycin biosynthetic pathway to generate variant glycopeptides.

Jon S Thorson, Jiqing Jiang, Daniel Kahne, 2002, Chemistry & biology.

Pd/Cu-catalyzed couplings of β-amino esters with aryl bromides. Synthesis of chiral 1,2,3,4-tetrahydro-4-oxo-2-alkyl-1-quinolines

D. Ma, Jiqing Jiang, 1998 .

Studies on the substrate specificity of Escherichia coli galactokinase.

Jie Yang, J. Thorson, Jingjing Zhao, 2003, Organic letters.

Discovery of trifluoromethyl(pyrimidin-2-yl)azetidine-2-carboxamides as potent, orally bioavailable TGR5 (GPBAR1) agonists: structure-activity relationships, lead optimization, and chronic in vivo efficacy.

P. McNamara, Chun Xing Li, Yang Yang, 2014, Journal of medicinal chemistry.

Recent Progress in Sensing Technology Based on Triboelectric Nanogenerators in Dynamic Behaviors

Zhicheng Zhang, Xianglong Zheng, He Zhang, 2022, Sensors.

Design, synthesis, and structure-activity-relationship of phenyl imidazoles as potent Smoothened antagonists.

D. Han, T. Tuntland, N. Englund, 2012, Bioorganic & medicinal chemistry letters.

Polyfunctionalized pyrrolidinones via the coupling of N,N- disubstituted β-amino esters with ethyl glyoxalate

D. Ma, Jiqing Jiang, 1998 .

Expanding the Pyrimidine Diphosphosugar Repertoire: The Chemoenzymatic Synthesis of Amino- and Acetamidoglucopyranosyl Derivatives.

J. Thorson, J. Biggins, Jiqing Jiang, 2001, Angewandte Chemie.

Structure of the coat protein in fd filamentous bacteriophage particles determined by solid-state NMR spectroscopy

Sungjoon Kim, Jiqing Jiang, Jonathan S. Melnick, 2007 .

Antibiotic optimization via in vitro glycorandomization

J. Thorson, Changsheng Zhang, C. Albermann, 2003, Nature Biotechnology.

The in vitro Characterization of Polyene Glycosyltransferases AmphDI and NysDI

Rocco Moretti, J. Thorson, Changsheng Zhang, 2008, Chembiochem : a European journal of chemical biology.

Substrate specificity of NovM: implications for novobiocin biosynthesis and glycorandomization.

J. Thorson, D. Nikolov, J. Biggins, 2003, Organic letters.

A General Enzymatic Method for the Synthesis of Natural and “Unnatural” UDP- and TDP-Nucleotide Sugars

J. Thorson, Jiqing Jiang, A. Biggins, 2000 .

Discovery of NVP-LDE225, a Potent and Selective Smoothened Antagonist.

M. Warmuth, J. Williams, S. Peukert, 2010, ACS medicinal chemistry letters.

Application of the Nucleotidylyltransferase Ep toward the Chemoenzymatic Synthesis of dTDP‐Desosamine Analogues

J. Thorson, C. Albermann, Jiqing Jiang, 2003, Chembiochem : a European journal of chemical biology.

Natures Carbohydrate Chemists The Enzymatic Glycosylation of Bioactive Bacterial Metabolites

J. Thorson, J. Biggins, Jiqing Jiang, 2001 .

A new strategy for the stereospecific syntheses of C‐furanosides

Bing Yang, Jiqing Jiang, Hou-Ming Wu, 1997 .

Expanding pyrimidine diphosphosugar libraries via structure-based nucleotidylyltransferase engineering

Jon S Thorson, Jiqing Jiang, J. Thorson, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Structure, mechanism and engineering of a nucleotidylyltransferase as a first step toward glycorandomization

P. Jeffrey, J. Thorson, K. Rajashankar, 2001, Nature Structural Biology.

Synthesis of (2S,1′ S,2′ S)-2-methyl-2-(carboxycyclopropyl)glycine and (S)-2-amino-2-methyl-4-phosphonobutyric acid from l-alanine

Zhenqiang Yang, D. Ma, Jiqing Jiang, 1997 .

Identification of NVP-TAE684, a potent, selective, and efficacious inhibitor of NPM-ALK

Peter G. Schultz, Yi Liu, Jiqing Jiang, 2007, Proceedings of the National Academy of Sciences.

Efficacy and Tolerability of Pyrazolo[1,5-a]pyrimidine RET Kinase Inhibitors for the Treatment of Lung Adenocarcinoma.

Nanxin Li, J. Shaffer, S. Kasibhatla, 2020, ACS medicinal chemistry letters.

Synthesis, structure-activity relationships, and in vivo efficacy of the novel potent and selective anaplastic lymphoma kinase (ALK) inhibitor 5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (LDK378) currently in phase 1 and phase 2

Sungjoon Kim, Nanxin Li, M. Warmuth, 2013, Journal of medicinal chemistry.

Antitarget Selectivity and Tolerability of Novel Pyrrolo[2,3-d]pyrimidine RET Inhibitors.

Nanxin Li, J. Shaffer, S. Kasibhatla, 2021, ACS medicinal chemistry letters.