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Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (−)-Deschloromytilipin A and (−)-Danicalipin A

Journal of the American Chemical Society, 2016-04, Vol.138 (15), p.5150-5158

2016

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Catalytic Enantioselective Dibromination of Allylic Alcohols

Journal of the American Chemical Society, 2013-09, Vol.135 (35), p.12960-12963

2013

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Flow Chemistry Syntheses of Styrenes, Unsymmetrical Stilbenes and Branched Aldehydes

ChemCatChem, 2013-01, Vol.5 (1), p.159-172

2013

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Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products

Chemical reviews, 2016-07, Vol.116 (14), p.7818-7853

2016

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Continuous Multiple Liquid–Liquid Separation: Diazotization of Amino Acids in Flow

Organic letters, 2012-08, Vol.14 (16), p.4246-4249

2012

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Rotamers or Diastereomers? An Overlooked NMR Solution

Journal of organic chemistry, 2012-06, Vol.77 (11), p.5198-5202

2012

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Property-Based Drug Design Merits a Nobel Prize

Journal of medicinal chemistry, 2024-06

2024

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Discovery of Potent, Selective, and Orally Bioavailable Inhibitors of USP7 with In Vivo Antitumor Activity

Journal of medicinal chemistry, 2020-05, Vol.63 (10), p.5398-5420

2020

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Structure-Based Design of Potent, Selective, and Orally Bioavailable VPS34 Kinase Inhibitors

Journal of medicinal chemistry, 2022-09, Vol.65 (17), p.11500-11512

2022

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Novel Piperidinyl-Azetidines as Potent and Selective CCR4 Antagonists Elicit Antitumor Response as a Single Agent and in Combination with Checkpoint Inhibitors

Journal of medicinal chemistry, 2020-08, Vol.63 (15), p.8584-8607

2020

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Novel, Selective Inhibitors of USP7 Uncover Multiple Mechanisms of Antitumor Activity In Vitro and In Vivo

Molecular cancer therapeutics, 2020-10, Vol.19 (10), p.1970-1980

2020

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EBV+ tumors exploit tumor cell-intrinsic and -extrinsic mechanisms to produce regulatory T cell-recruiting chemokines CCL17 and CCL22

PLoS pathogens, 2022-01, Vol.18 (1), p.e1010200-e1010200

2022

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Discovery of a Potent and Selective CCR4 Antagonist That Inhibits Treg Trafficking into the Tumor Microenvironment

Journal of medicinal chemistry, 2019-07, Vol.62 (13), p.6190-6213

2019

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Potent GCN2 Inhibitor Capable of Reversing MDSC-Driven T Cell Suppression Demonstrates In Vivo Efficacy as a Single Agent and in Combination with Anti-Angiogenesis Therapy

Journal of medicinal chemistry, 2022-10, Vol.65 (19), p.12895-12924

2022

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Enantioselective Total Synthesis and Confirmation of the Absolute and Relative Stereochemistry of Streptorubin B

Journal of the American Chemical Society, 2011-02, Vol.133 (6), p.1799-1804

2011

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Discovery of a Potent and Selective CCR4 Antagonist That Inhibits T reg Trafficking into the Tumor Microenvironment

Journal of medicinal chemistry, 2019-07, Vol.62 (13), p.6190-6213

2019

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A Synthesis of the Carbocyclic Core of Maoecrystal V

Organic letters, 2010-07, Vol.12 (13), p.3010-3013

2010

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Elimination of Butylcycloheptylprodigiosin as a Known Natural Product Inspired by an Evolutionary Hypothesis for Cyclic Prodigiosin Biosynthesis

Journal of natural products (Washington, D.C.), 2013-10, Vol.76 (10), p.1937-1945

2013

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EBV.sup.+ tumors exploit tumor cell-intrinsic and -extrinsic mechanisms to produce regulatory T cell-recruiting chemokines CCL17 and CCL22

PLoS pathogens, 2022-01, Vol.18 (1)

2022

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A total synthesis of the ammonium ionophore, (−)-enniatin B

Tetrahedron letters, 2012-08, Vol.53 (32), p.4077-4079

2012

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ChemInform Abstract: Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (‐)‐Deschloromytilipin A and (‐)‐Danicalipin A

ChemInform, 2016-09, Vol.47 (39), p.no-no

2016

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ChemInform Abstract: Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products

ChemInform, 2016-09, Vol.47 (39), p.no-no

2016

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ChemInform Abstract: Catalytic Chemo-, Regio-, and Enantioselective Bromochlorination of Allylic Alcohols

ChemInform, 2015-09, Vol.46 (35), p.no-no

2015

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ChemInform Abstract: Catalytic Enantioselective Dibromination of Allylic Alcohols

ChemInform, 2014-02, Vol.45 (8), p.no-no

2014

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ChemInform Abstract: Enantioselective Total Synthesis and Confirmation of the Absolute and Relative Stereochemistry of Streptorubin B

ChemInform, 2011-05, Vol.42 (19), p.no-no

2011

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Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (−)-Deschloromytilipin A and (−)-Danicalipin A

Catalytic Enantioselective Dibromination of Allylic Alcohols

Flow Chemistry Syntheses of Styrenes, Unsymmetrical Stilbenes and Branched Aldehydes

Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products

Continuous Multiple Liquid–Liquid Separation: Diazotization of Amino Acids in Flow

Rotamers or Diastereomers? An Overlooked NMR Solution

Property-Based Drug Design Merits a Nobel Prize

Discovery of Potent, Selective, and Orally Bioavailable Inhibitors of USP7 with In Vivo Antitumor Activity

Structure-Based Design of Potent, Selective, and Orally Bioavailable VPS34 Kinase Inhibitors

Novel Piperidinyl-Azetidines as Potent and Selective CCR4 Antagonists Elicit Antitumor Response as a Single Agent and in Combination with Checkpoint Inhibitors

Novel, Selective Inhibitors of USP7 Uncover Multiple Mechanisms of Antitumor Activity In Vitro and In Vivo

EBV+ tumors exploit tumor cell-intrinsic and -extrinsic mechanisms to produce regulatory T cell-recruiting chemokines CCL17 and CCL22

Discovery of a Potent and Selective CCR4 Antagonist That Inhibits Treg Trafficking into the Tumor Microenvironment

Potent GCN2 Inhibitor Capable of Reversing MDSC-Driven T Cell Suppression Demonstrates In Vivo Efficacy as a Single Agent and in Combination with Anti-Angiogenesis Therapy

Enantioselective Total Synthesis and Confirmation of the Absolute and Relative Stereochemistry of Streptorubin B

Discovery of a Potent and Selective CCR4 Antagonist That Inhibits T reg Trafficking into the Tumor Microenvironment

A Synthesis of the Carbocyclic Core of Maoecrystal V

Elimination of Butylcycloheptylprodigiosin as a Known Natural Product Inspired by an Evolutionary Hypothesis for Cyclic Prodigiosin Biosynthesis

EBV.sup.+ tumors exploit tumor cell-intrinsic and -extrinsic mechanisms to produce regulatory T cell-recruiting chemokines CCL17 and CCL22

A total synthesis of the ammonium ionophore, (−)-enniatin B

ChemInform Abstract: Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (‐)‐Deschloromytilipin A and (‐)‐Danicalipin A

ChemInform Abstract: Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products

ChemInform Abstract: Catalytic Chemo-, Regio-, and Enantioselective Bromochlorination of Allylic Alcohols

ChemInform Abstract: Catalytic Enantioselective Dibromination of Allylic Alcohols

ChemInform Abstract: Enantioselective Total Synthesis and Confirmation of the Absolute and Relative Stereochemistry of Streptorubin B

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