Year |
Citation |
Score |
2022 |
Shen K, Lowary TL. Synthesis of the Canetti Lipooligosaccharide II Nonasaccharide. Organic Letters. PMID 36005851 DOI: 10.1021/acs.orglett.2c02518 |
0.5 |
|
2021 |
Lowary T, Shen K, Bai B, Liu YH. Synthesis of a Tridecasaccharide Lipooligosaccharide Antigen from the Opportunistic Pathogen Mycobacterium kansasii. Angewandte Chemie (International Ed. in English). PMID 34553821 DOI: 10.1002/anie.202111549 |
0.563 |
|
2018 |
Sigal GB, Pinter A, Lowary TL, Kawasaki M, Li A, Mathew A, Tsionsky M, Zheng RB, Plisova T, Shen K, Katsuragi K, Choudhary A, Honnen WJ, Nahid P, Denkinger CM, et al. A novel sensitive immunoassay targeting the MTX-Lipoarabinomannan epitope meets the WHO's performance target for Tuberculosis diagnosis. Journal of Clinical Microbiology. PMID 30257899 DOI: 10.1128/Jcm.01338-18 |
0.4 |
|
2018 |
Zhang L, Shen K, Taha HA, Lowary TL. Stereocontrolled synthesis of α-xylofuranosides using a conformationally-restricted donor. The Journal of Organic Chemistry. PMID 29895148 DOI: 10.1021/Acs.Joc.8B00410 |
0.512 |
|
2018 |
Choudhary A, Patel D, Honnen W, Lai Z, Prattipati RS, Zheng RB, Hsueh YC, Gennaro ML, Lardizabal A, Restrepo BI, Garcia-Viveros M, Joe M, Bai Y, Shen K, Sahloul K, et al. Characterization of the Antigenic Heterogeneity of Lipoarabinomannan, the Major Surface Glycolipid of, and Complexity of Antibody Specificities toward This Antigen. Journal of Immunology (Baltimore, Md. : 1950). PMID 29610143 DOI: 10.4049/Jimmunol.1701673 |
0.425 |
|
2017 |
Zheng RB, Jégouzo SAF, Joe M, Bai Y, Tran HA, Shen K, Saupe J, Xia L, Ahmed MF, Liu YH, Patil PS, Tripathi A, Hung SC, Taylor ME, Lowary TL, et al. Insights into mycobacteria interactions with the host innate immune system from a novel array of synthetic mycobacterial glycans. Acs Chemical Biology. PMID 29048873 DOI: 10.1021/Acschembio.7B00797 |
0.668 |
|
2016 |
Shen K, Ma X, Zhu C, Wu X, Jia H. Safety and Efficacy of Trastuzumab Emtansine in Advanced Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer: a Meta-analysis. Scientific Reports. 6: 23262. PMID 26979925 DOI: 10.1038/srep23262 |
0.337 |
|
2015 |
Poopari MR, Dezhahang Z, Shen K, Wang L, Lowary TL, Xu Y. Absolute Configuration and Conformation of Two Fráter-Seebach Alkylation Reaction Products by Film VCD and ECD Spectroscopic Analyses. The Journal of Organic Chemistry. 80: 428-37. PMID 25437116 DOI: 10.1021/Jo502438A |
0.463 |
|
2012 |
Shen K, Liu X, Lin L, Feng X. Recent progress in enantioselective synthesis of C3-functionalized oxindoles: rare earth metals take action Chem. Sci.. 3: 327-334. DOI: 10.1039/C1Sc00544H |
0.526 |
|
2011 |
Shen K, Liu X, Wang G, Lin L, Feng X. Facile and efficient enantioselective hydroxyamination reaction: synthesis of 3-hydroxyamino-2-oxindoles using nitrosoarenes. Angewandte Chemie (International Ed. in English). 50: 4684-8. PMID 21495145 DOI: 10.1002/Anie.201100758 |
0.594 |
|
2010 |
Li W, Wang J, Hu X, Shen K, Wang W, Chu Y, Lin L, Liu X, Feng X. Catalytic asymmetric Roskamp reaction of alpha-alkyl-alpha-diazoesters with aromatic aldehydes: highly enantioselective synthesis of alpha-alkyl-beta-keto esters. Journal of the American Chemical Society. 132: 8532-3. PMID 20527752 DOI: 10.1021/Ja102832F |
0.655 |
|
2010 |
Cai Y, Wang W, Shen K, Wang J, Hu X, Lin L, Liu X, Feng X. Highly enantioselective alpha-chlorination of cyclic beta-ketoesters catalyzed by N,N'-dioxide using NCS as the chlorine source. Chemical Communications (Cambridge, England). 46: 1250-2. PMID 20449266 DOI: 10.1039/B922769E |
0.68 |
|
2010 |
Yang Z, Wang Z, Bai S, Shen K, Chen D, Liu X, Lin L, Feng X. Highly enantioselective synthesis of 3-amino-2-oxindole derivatives: catalytic asymmetric alpha-amination of 3-substituted 2-oxindoles with a chiral scandium complex. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 6632-7. PMID 20408167 DOI: 10.1002/Chem.201000126 |
0.695 |
|
2010 |
Shen K, Liu X, Zheng K, Li W, Hu X, Lin L, Feng X. Catalytic asymmetric synthesis of 3-(alpha-hydroxy-beta-carbonyl) oxindoles by a Sc(III)-catalyzed direct aldol-type reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3736-42. PMID 20175165 DOI: 10.1002/Chem.200903471 |
0.663 |
|
2010 |
Shen K, Liu X, Wang W, Wang G, Cao W, Li W, Hu X, Lin L, Feng X. Highly enantioselective synthesis of 1,3-bis(hydroxymethyl)-2-oxindoles from unprotected oxindoles and formalin using a chiral NdIII complex Chemical Science. 1: 590. DOI: 10.1039/C0Sc00385A |
0.652 |
|
2009 |
Wang J, Wang W, Li W, Hu X, Shen K, Tan C, Liu X, Feng X. Asymmetric cyanation of aldehydes, ketones, aldimines, and ketimines catalyzed by a versatile catalyst generated from cinchona alkaloid, achiral substituted 2,2'-biphenol and tetraisopropyl titanate. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11642-59. PMID 19774566 DOI: 10.1002/Chem.200900936 |
0.666 |
|
2009 |
Shen K, Liu X, Cai Y, Lin L, Feng X. Facile and efficient enantioselective Strecker reaction of ketimines by chiral sodium phosphate. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 6008-14. PMID 19418513 DOI: 10.1002/Chem.200900210 |
0.714 |
|
2009 |
Feng X, Wang W, Shen K, Hu X, Wang J, Liu X. Highly Enantioselective Synthesis
of α-Diazo-β-hydroxy Esters Using a Bifunctional
Titanium Complex Synlett. 2009: 1655-1658. DOI: 10.1055/S-0029-1217322 |
0.627 |
|
2009 |
Wang W, Shen K, Hu X, Wang J, Liu X, Feng X. ChemInform Abstract: Highly Enantioselective Synthesis of α-Diazo-β-hydroxy Esters Using a Bifunctional Titanium Complex. Cheminform. 40. DOI: 10.1002/chin.200943083 |
0.399 |
|
2008 |
Shen K, Liu X, Li Q, Feng X. Highly enantioselective cyanosilylation of ketones catalyzed by a bifunctional Ti(IV) complex Tetrahedron. 64: 147-153. DOI: 10.1016/J.Tet.2007.10.093 |
0.609 |
|
2006 |
Li Q, Liu X, Wang J, Shen K, Feng X. Corrigendum to “Asymmetric cyanosilylation of ketones catalyzed by novel chiral N,N′-dioxide titanium complexes” Tetrahedron Letters. 47: 7395-7396. DOI: 10.1016/J.Tetlet.2006.08.031 |
0.608 |
|
2006 |
Li Q, Liu X, Wang J, Shen K, Feng X. Asymmetric Cyanosilylation of Ketones Catalyzed by Novel Chiral N,N′-Dioxide Titanium Complexes. Cheminform. 37. DOI: 10.1016/J.Tetlet.2006.04.003 |
0.645 |
|
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