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C‑Glycosidation of Unprotected Di- and Trisaccharide Aldopyranoses with Ketones Using Pyrrolidine-Boric Acid Catalysis

Journal of organic chemistry, 2018-04, Vol.83 (8), p.4581-4597

2018

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Structure- and fragment-based approaches to protease inhibition

Current topics in medicinal chemistry, 2006-02, Vol.6 (4), p.317-329

2006

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Chelator Fragment Libraries for Targeting Metalloproteinases

ChemMedChem, 2010-02, Vol.5 (2), p.195-199

2010

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Aldol reactions of 1,2-diketones catalyzed by amines to afford furanose derivatives

Tetrahedron letters, 2015-01, Vol.56 (5), p.735-738

2015

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Direct synthesis of C-glycosides from unprotected 2-N-acyl-aldohexoses via aldol condensation-oxa-Michael reactions with unactivated ketones

Organic & biomolecular chemistry, 2016-01, Vol.14 (1), p.259-264

2016

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Biochemical Characterization of the Cellular Glycosylphosphatidylinositol-linked Membrane Type-6 Matrix Metalloproteinase

The Journal of biological chemistry, 2010-05, Vol.285 (21), p.16076-16086

2010

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Efficient Synthetic Inhibitors of Anthrax Lethal Factor

Proceedings of the National Academy of Sciences - PNAS, 2005-07, Vol.102 (27), p.9499-9504

2005

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Synthesis of Furanose Spirooxindoles via 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-Catalyzed Aldol Reactions of a Pyruvic Aldehyde Derivative

Asian journal of organic chemistry, 2014-04, Vol.3 (4), p.391-394

2014

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Anthrax Lethal Factor Protease Inhibitors: Synthesis, SAR, and Structure-Based 3D QSAR Studies

Journal of medicinal chemistry, 2006-01, Vol.49 (1), p.27-30

2006

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Direct synthesis of C-glycosides from unprotected 2-N-acyl-aldohexoses via aldol condensation-oxa-Michael reactions with unactivated ketonesElectronic supplementary information (ESI) available: Synthesis and characterization of compounds, and X-ray crystal structures of compounds 2a and 6b. CCDC 1422504 and 1422505. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ob02094h

2015-12

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Structure–activity relationship studies of a novel series of anthrax lethal factor inhibitors

Bioorganic & medicinal chemistry, 2009-05, Vol.17 (9), p.3352-3368

2009

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Rhodanine Derivatives as Selective Protease Inhibitors Against Bacterial Toxins

Chemical biology & drug design, 2008-02, Vol.71 (2), p.131-139

2008

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A high-throughput screening approach to anthrax lethal factor inhibition

Bioorganic chemistry, 2007-08, Vol.35 (4), p.306-312

2007

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C-Glycosidation of Unprotected Aldopentoses with Ketones Using Proline-Triethylamine as Catalyst

Heterocycles, 2019, Vol.99 (1), p.633

2019

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Novel Pharmacophore Model for the Design of Anthrax Lethal Factor Inhibitors

Chemical biology & drug design, 2010-09, Vol.76 (3), p.263-268

2010

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Element selective characterization of stability and reactivity of selenium species in selenized yeast

Journal of analytical atomic spectrometry, 2004-01, Vol.19 (1), p.65

2004

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Targeting Metalloproteins by Fragment-Based Lead Discovery

Chemical biology & drug design, 2011-08, Vol.78 (2), p.211-223

2011

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Identification and Synthesis of a Novel Selenium−Sulfur Amino Acid Found in Selenized Yeast: Rapid Indirect Detection NMR Methods for Characterizing Low-Level Organoselenium Compounds in Complex Matrices

Journal of agricultural and food chemistry, 2004-06, Vol.52 (12), p.3761-3771

2004

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Targeting Metallo-proteins by Fragment-Based Lead Discovery

Chemical biology & drug design, 2011-06, Vol.78 (2), p.211-223

2011

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The Sulfur Chemistry of Shiitake Mushroom

Journal of the American Chemical Society, 2004-01, Vol.126 (2), p.458-459

2004

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WITHDRAWN: A High-throughput Screening Approach to Anthrax Lethal Factor Inhibition

Bioorganic chemistry, 2006-12

2006

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Studies of organosulfur and organoselenium compounds from selenized yeast and mushrooms

Johnson, Sherida

2006

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Insights into the Chemical Biology of Selenium

Phosphorus, sulfur, and silicon and the related elements, 2008-04, Vol.183 (4), p.924-930

2008

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ChemInform Abstract: Aldol Reactions of 1,2-Diketones Catalyzed by Amines to Afford Furanose Derivatives

ChemInform, 2015-06, Vol.46 (23), p.no-no

2015

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New compounds with extended structure latticesfrom the reactions of cuprous iodide with cyclicpolydisulfides

Polyhedron, 1998-08, Vol.17 (17), p.2775-2780

1998

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C‑Glycosidation of Unprotected Di- and Trisaccharide Aldopyranoses with Ketones Using Pyrrolidine-Boric Acid Catalysis

Structure- and fragment-based approaches to protease inhibition

Chelator Fragment Libraries for Targeting Metalloproteinases

Aldol reactions of 1,2-diketones catalyzed by amines to afford furanose derivatives

Direct synthesis of C-glycosides from unprotected 2-N-acyl-aldohexoses via aldol condensation-oxa-Michael reactions with unactivated ketones

Biochemical Characterization of the Cellular Glycosylphosphatidylinositol-linked Membrane Type-6 Matrix Metalloproteinase

Efficient Synthetic Inhibitors of Anthrax Lethal Factor

Synthesis of Furanose Spirooxindoles via 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-Catalyzed Aldol Reactions of a Pyruvic Aldehyde Derivative

Anthrax Lethal Factor Protease Inhibitors: Synthesis, SAR, and Structure-Based 3D QSAR Studies

Structure–activity relationship studies of a novel series of anthrax lethal factor inhibitors

Rhodanine Derivatives as Selective Protease Inhibitors Against Bacterial Toxins

A high-throughput screening approach to anthrax lethal factor inhibition

C-Glycosidation of Unprotected Aldopentoses with Ketones Using Proline-Triethylamine as Catalyst

Novel Pharmacophore Model for the Design of Anthrax Lethal Factor Inhibitors

Element selective characterization of stability and reactivity of selenium species in selenized yeast

Targeting Metalloproteins by Fragment-Based Lead Discovery

Identification and Synthesis of a Novel Selenium−Sulfur Amino Acid Found in Selenized Yeast: Rapid Indirect Detection NMR Methods for Characterizing Low-Level Organoselenium Compounds in Complex Matrices

Targeting Metallo-proteins by Fragment-Based Lead Discovery

The Sulfur Chemistry of Shiitake Mushroom

WITHDRAWN: A High-throughput Screening Approach to Anthrax Lethal Factor Inhibition

Studies of organosulfur and organoselenium compounds from selenized yeast and mushrooms

Insights into the Chemical Biology of Selenium

ChemInform Abstract: Aldol Reactions of 1,2-Diketones Catalyzed by Amines to Afford Furanose Derivatives

New compounds with extended structure latticesfrom the reactions of cuprous iodide with cyclicpolydisulfides

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