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Concise Synthesis of Pauciflorol F Using a Larock Annulation

Organic letters, 2009-12, Vol.11 (23), p.5450-5453

2009

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Intramolecular C(sp3)–H amination

Chemical science (Cambridge), 2013-09, Vol.4 (11), p.4092

2013

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An approach to the synthesis of dimeric resveratrol natural products via a palladium-catalyzed domino reaction

Tetrahedron letters, 2009-04, Vol.50 (17), p.1969-1972

2009

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O–H hydrogen bonding promotes H-atom transfer from α C–H bonds for C-alkylation of alcohols

Science (American Association for the Advancement of Science), 2015-09, Vol.349 (6255), p.1532-1536

2015

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Targeting Metabolism of Extracellular Nucleotides via Inhibition of Ectonucleotidases CD73 and CD39

Journal of medicinal chemistry, 2020-11, Vol.63 (22), p.13444-13465

2020

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Selective Radical–Radical Cross-Couplings: Design of a Formal β‑Mannich Reaction

Journal of the American Chemical Society, 2015-07, Vol.137 (26), p.8404-8407

2015

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Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor

Tetrahedron, 2019-08, Vol.75 (32), p.4222-4227

2019

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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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Chichibabin-Type Direct Alkylation of Pyridyl Alcohols with Alkyl Lithium Reagents

Organic letters, 2012-11, Vol.14 (21), p.5400-5403

2012

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Discovery of Potent and Selective Non-Nucleotide Small Molecule Inhibitors of CD73

Journal of medicinal chemistry, 2020-04, Vol.63 (8), p.3935-3955

2020

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Intramolecular C(sp3)N Coupling by Oxidation of Benzylic C,N-Dianions

Angewandte Chemie (International ed.), 2013-02, Vol.52 (8), p.2194-2197

International ed. in English, 2013

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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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O-H hydrogen bonding promotes H-atom transfer from [alpha] C-H bonds for C-alkylation of alcohols

Science (American Association for the Advancement of Science), 2015-09, Vol.349 (6255), p.1532-1536

2015

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Intramolecular C(sp 3 )N Coupling by Oxidation of Benzylic C,N‐Dianions

Angewandte Chemie, 2013-02, Vol.125 (8), p.2250-2253

2013

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Synthesis of 1-Substituted Benzo[c]isoxazol-3(1H)-imines via Tandem Nitroso-Ene/Intramolecular Cyclizations of 2-Nitrosobenzonitrile

Journal of organic chemistry, 2008-04, Vol.73 (8), p.3288-3291

2008

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Corrigendum to Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor® [Tetrahedron. 75(32), 9 August 2019, 4222-4227]

Tetrahedron, 2023-07, Vol.141, p.133493, Article 133493

2023

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Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor

Tetrahedron, 2023-07, Vol.141, p.133494, Article 133494

2023

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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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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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Abstract 1756: Discovery and characterization of AB680, a potent and selective small-molecule CD73 inhibitor for cancer immunotherapy

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.1756-1756

2018

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Abstract 3168: Methods for assessment of the “adenosine fingerprint” in clinical trials of AB928

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.3168-3168

2019

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Abstract A10: The dual A2aR/A2bR antagonist AB928 reverses adenosine-mediated immune suppression and inhibits tumor growth in vivo

Cancer immunology research, 2020-04, Vol.8 (4_Supplement), p.A10-A10

2020

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ChemInform Abstract: Intramolecular C(sp3)-H Amination

ChemInform, 2014-01, Vol.45 (1), p.no-no

2014

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Concise Synthesis of Pauciflorol F Using a Larock Annulation

Intramolecular C(sp3)–H amination

An approach to the synthesis of dimeric resveratrol natural products via a palladium-catalyzed domino reaction

O–H hydrogen bonding promotes H-atom transfer from α C–H bonds for C-alkylation of alcohols

Targeting Metabolism of Extracellular Nucleotides via Inhibition of Ectonucleotidases CD73 and CD39

Selective Radical–Radical Cross-Couplings: Design of a Formal β‑Mannich Reaction

Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor

Discovery of AB680: A Potent and Selective Inhibitor of CD73

Chichibabin-Type Direct Alkylation of Pyridyl Alcohols with Alkyl Lithium Reagents

Discovery of Potent and Selective Non-Nucleotide Small Molecule Inhibitors of CD73

Intramolecular C(sp3)N Coupling by Oxidation of Benzylic C,N-Dianions

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

O-H hydrogen bonding promotes H-atom transfer from [alpha] C-H bonds for C-alkylation of alcohols

Intramolecular C(sp 3 )N Coupling by Oxidation of Benzylic C,N‐Dianions

Synthesis of 1-Substituted Benzo[c]isoxazol-3(1H)-imines via Tandem Nitroso-Ene/Intramolecular Cyclizations of 2-Nitrosobenzonitrile

Corrigendum to Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor® [Tetrahedron. 75(32), 9 August 2019, 4222-4227]

Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor

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

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

Abstract 1756: Discovery and characterization of AB680, a potent and selective small-molecule CD73 inhibitor for cancer immunotherapy

Abstract 3168: Methods for assessment of the “adenosine fingerprint” in clinical trials of AB928

Abstract A10: The dual A2aR/A2bR antagonist AB928 reverses adenosine-mediated immune suppression and inhibits tumor growth in vivo

ChemInform Abstract: Intramolecular C(sp3)-H Amination

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