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Gold(i)-catalyzed enantioselective bromocyclization reactions of allenes

Chemical science (Cambridge), 2013-01, Vol.4 (9), p.3427

2013

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A Nucleophilic Strategy for Enantioselective Intermolecular α‑Amination: Access to Enantioenriched α‑Arylamino Ketones

Journal of the American Chemical Society, 2015-06, Vol.137 (24), p.7632-7635

2015

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Enantioselective Synthesis of N,S‐Acetals by an Oxidative Pummerer‐Type Transformation using Phase‐Transfer Catalysis

Angewandte Chemie International Edition, 2018-01, Vol.57 (2), p.589-593

International ed. in English, 2018

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Discovery of AB680: A Potent and Selective Inhibitor of CD73

Journal of medicinal chemistry, 2020-10, Vol.63 (20), p.11448-11468

2020

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Discovery of Potent and Selective Methylenephosphonic Acid CD73 Inhibitors

Journal of medicinal chemistry, 2021-01, Vol.64 (1), p.845-860

2021

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Discovery of Potent and Selective PI3Kγ Inhibitors

Journal of medicinal chemistry, 2020-10, Vol.63 (19), p.11235-11257

2020

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Design, Synthesis, and Structure-Activity Relationship Optimization of Pyrazolopyrimidine Amide Inhibitors of Phosphoinositide 3-Kinase γ (PI3Kγ)

Journal of medicinal chemistry, 2022-01, Vol.65 (2), p.1418-1444

2022

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Discovery of Potent and Selective 7‑Azaindole Isoindolinone-Based PI3Kγ Inhibitors

ACS medicinal chemistry letters, 2020-11, Vol.11 (11), p.2244-2252

2020

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Enantioselective Synthesis of N,S‐Acetals by an Oxidative Pummerer‐Type Transformation using Phase‐Transfer Catalysis

Angewandte Chemie, 2018-01, Vol.130 (2), p.598-602

2018

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Development of a Robust and Scalable Synthetic Route for a Potent and Selective Isoindolinone PI3Kγ Inhibitor

Organic process research & development, 2022-10, Vol.26 (10), p.2915-2925

2022

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Improved synthesis of sterically encumbered heteroaromatic biaryls from aromatic β-keto esters

Tetrahedron letters, 2020-05, Vol.61 (20), p.151855, Article 151855

2020

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Enantioselective Synthesis of N,S-Acetals by an Oxidative Pummerer Type Transformation Using Anionic Phase-Transfer Catalysis

Angewandte Chemie International Edition, 2017-12, Vol.57 (2), p.589-593

2017

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Development of a Scalable and Practical Synthesis of AB928, a Dual A 2a /A 2b Receptor Antagonist

Organic process research & development, 2020-07, Vol.24 (7), p.1254-1261

2020

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Kinetic and Mechanistic Characterization of a Potent and Selective Inhibitor for Human AXL Receptor Tyrosine Kinase

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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Stabilization and functionalization of single-walled carbon nanotubes with polyvinylpyrrolidone copolymers for applications in aqueous media

Journal of polymer science. Part A, Polymer chemistry, 2015-01, Vol.53 (2), p.337-343

2015

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Abstract P253: Potent and selective AXL tyrosine kinase inhibition demonstrates significant anti-tumor efficacy in combination with standard of care therapeutics in preclinical models

Molecular cancer therapeutics, 2021-12, Vol.20 (12_Supplement), p.P253-P253

2021

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Abstract 518: AB801 is a highly potent and selective AXL kinase inhibitor that demonstrates significant anti-tumor activity

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.518-518

2023

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Abstract A162: AB928, a dual antagonist of the A2aR and A2bR adenosine receptors, relieves adenosine-mediated immune suppression

Cancer immunology research, 2019-02, Vol.7 (2_Supplement), p.A162-A162

2019

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ChemInform Abstract: Gold(I)-Catalyzed Enantioselective Bromocyclization Reactions of Allenes

ChemInform, 2014-02, Vol.45 (6), p.no-no

2014

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Development of a Scalable and Practical Synthesis of AB928, a Dual A2a/A2b Receptor Antagonist

Organic process research & development, 2020-07, Vol.24 (7), p.1254-1261

2020

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ChemInform Abstract: A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones

ChemInform, 2015-12, Vol.46 (48), p.no-no

2015

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ChemInform Abstract: A Nucleophilic Strategy for Enantioselective Intermolecular [alpha]-Amination: Access to Enantioenriched [alpha]-Arylamino Ketones

ChemInform, 2015-12, Vol.46 (48)

2015

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Enantioselective Gold-Catalyzed Synthesis of Heterocyclic Compounds

Au-Catalyzed Synthesis and Functionalization of Heterocycles, 2016, Vol.46, p.227-248

2016

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Changes in anger and aggression after treatment for PTSD in active duty military

Journal of clinical psychology, 2020-03, Vol.76 (3), p.493-507

2020

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Accuracy of electrical impedance cardiography for measuring cardiac output in children with congenital heart defects

The American journal of cardiology, 1988-03, Vol.61 (8), p.612-616

1988

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Gold(i)-catalyzed enantioselective bromocyclization reactions of allenes

A Nucleophilic Strategy for Enantioselective Intermolecular α‑Amination: Access to Enantioenriched α‑Arylamino Ketones

Enantioselective Synthesis of N,S‐Acetals by an Oxidative Pummerer‐Type Transformation using Phase‐Transfer Catalysis

Discovery of AB680: A Potent and Selective Inhibitor of CD73

Discovery of Potent and Selective Methylenephosphonic Acid CD73 Inhibitors

Discovery of Potent and Selective PI3Kγ Inhibitors

Design, Synthesis, and Structure-Activity Relationship Optimization of Pyrazolopyrimidine Amide Inhibitors of Phosphoinositide 3-Kinase γ (PI3Kγ)

Discovery of Potent and Selective 7‑Azaindole Isoindolinone-Based PI3Kγ Inhibitors

Enantioselective Synthesis of N,S‐Acetals by an Oxidative Pummerer‐Type Transformation using Phase‐Transfer Catalysis

Development of a Robust and Scalable Synthetic Route for a Potent and Selective Isoindolinone PI3Kγ Inhibitor

Improved synthesis of sterically encumbered heteroaromatic biaryls from aromatic β-keto esters

Enantioselective Synthesis of N,S-Acetals by an Oxidative Pummerer Type Transformation Using Anionic Phase-Transfer Catalysis

Development of a Scalable and Practical Synthesis of AB928, a Dual A 2a /A 2b Receptor Antagonist

Kinetic and Mechanistic Characterization of a Potent and Selective Inhibitor for Human AXL Receptor Tyrosine Kinase

Stabilization and functionalization of single-walled carbon nanotubes with polyvinylpyrrolidone copolymers for applications in aqueous media

Abstract P253: Potent and selective AXL tyrosine kinase inhibition demonstrates significant anti-tumor efficacy in combination with standard of care therapeutics in preclinical models

Abstract 518: AB801 is a highly potent and selective AXL kinase inhibitor that demonstrates significant anti-tumor activity

Abstract A162: AB928, a dual antagonist of the A2aR and A2bR adenosine receptors, relieves adenosine-mediated immune suppression

ChemInform Abstract: Gold(I)-Catalyzed Enantioselective Bromocyclization Reactions of Allenes

Development of a Scalable and Practical Synthesis of AB928, a Dual A2a/A2b Receptor Antagonist

ChemInform Abstract: A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones

ChemInform Abstract: A Nucleophilic Strategy for Enantioselective Intermolecular [alpha]-Amination: Access to Enantioenriched [alpha]-Arylamino Ketones

Enantioselective Gold-Catalyzed Synthesis of Heterocyclic Compounds

Changes in anger and aggression after treatment for PTSD in active duty military

Accuracy of electrical impedance cardiography for measuring cardiac output in children with congenital heart defects

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