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Davis–Beirut Reaction: Diverse Chemistries of Highly Reactive Nitroso Intermediates in Heterocycle Synthesis

Accounts of chemical research, 2019-08, Vol.52 (8), p.2256-2265

2019

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Mechanistic interpretation of selective catalytic hydrogenation and isomerization of alkenes and dienes by ligand deactivated Pd nanoparticles

Nanoscale, 2015-11, Vol.7 (42), p.17786-17790

2015

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Diverting Reactive Intermediates Toward Unusual Chemistry: Unexpected Anthranil Products from Davis–Beirut Reaction

Journal of organic chemistry, 2017-10, Vol.82 (20), p.10875-10882

2017

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Colloidal Palladium Nanoparticles for Selective Hydrogenation of Styrene Derivatives with Reactive Functional Groups

ACS omega, 2019-12, Vol.4 (24), p.20819-20828

2019

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Ligand Oxidation Activates a Ruthenium(II) Precatalyst for C–H Hydroxylation

Journal of the American Chemical Society, 2024-08, Vol.146 (33), p.23067-23074

2024

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Novel 2‑(5-Imino‑5H‑isoquinolones[3,4‑b]quinoxalin-7-ylmethyl)-benzonitrile (DIQ3) and Other Related Derivatives Targeting Colon Cancer Cells: Syntheses and in Vitro Models

ACS omega, 2019-02, Vol.4 (2), p.3205-3212

2019

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Photochemical Preparation of 1,2-Dihydro-3 H-indazol-3-ones in Aqueous Solvent at Room Temperature

Journal of organic chemistry, 2018-12, Vol.83 (24), p.15493-15498

2018

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Photochemical Preparation of 1,2-Dihydro‑3H‑indazol-3-ones in Aqueous Solvent at Room Temperature

Journal of organic chemistry, 2018-12, Vol.83 (24), p.15493-15498

2018

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Accessing Multiple Classes of 2H‑Indazoles: Mechanistic Implications for the Cadogan and Davis–Beirut Reactions

Journal of the American Chemical Society, 2019-04, Vol.141 (15), p.6247-6253

2019

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Accessing Multiple Classes of 2 H-Indazoles: Mechanistic Implications for the Cadogan and Davis-Beirut Reactions

Journal of the American Chemical Society, 2019-04, Vol.141 (15), p.6247-6253

2019

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Davis–Beirut reaction inspired nitroso Diels–Alder reaction

Tetrahedron letters, 2021-04, Vol.69, p.152951, Article 152951

2021

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Davis-Beirut Reaction: A Photochemical Brønsted Acid Catalyzed Route to N -Aryl 2 H -Indazoles

Organic letters, 2019-08, Vol.21 (15), p.6058-6062

2019

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Davis–Beirut Reaction: A Photochemical Brønsted Acid Catalyzed Route to N‑Aryl 2H‑Indazoles

Organic letters, 2019-08, Vol.21 (15), p.6058-6062

2019

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N–N Bond Formation between Primary Amines and Nitrosos: Direct Synthesis of 2‑Substituted Indazolones with Mechanistic Insights

Organic letters, 2018-08, Vol.20 (16), p.4736-4739

2018

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Multicomponent Assembly of Highly Substituted Indoles by Dual Palladium-Catalyzed Coupling Reactions

Angewandte Chemie (International ed.), 2012-10, Vol.51 (42), p.10588-10591

International ed. in English, 2012

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1-BENZYLSPIRO[PIPERIDINE-4,1′-PYRIDO[3,4-b]indole] ‘co-potentiators’ for minimal function CFTR mutants

European journal of medicinal chemistry, 2021-01, Vol.209, p.112888-112888, Article 112888

2021

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High-Potency Phenylquinoxalinone Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activators

Journal of medicinal chemistry, 2017-03, Vol.60 (6), p.2401-2410

2017

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A Redox Isomerization Strategy for Accessing Modular Azobenzene Photoswitches with Near Quantitative Bidirectional Photoconversion

Organic letters, 2019-11, Vol.21 (21), p.8765-8770

2019

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Synthesis and evaluation of tetrahydropyrazolopyridine inhibitors of anion exchange protein SLC26A4 (pendrin)

Bioorganic & medicinal chemistry letters, 2019-08, Vol.29 (16), p.2119-2123

2019

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Davis–Beirut Reaction: Alkoxide versus Hydroxide Addition to the Key o‑Nitrosoimine Intermediate

Organic letters, 2018-03, Vol.20 (5), p.1308-1311

2018

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Correction to “Diverting Reactive Intermediates Toward Unusual Chemistry: Unexpected Anthranil Products from Davis–Beirut Reaction”

Journal of organic chemistry, 2017-12, Vol.82 (23), p.12946-12946

2017

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Phenylquinoxalinone CFTR activator as potential prosecretory therapy for constipation

Translational research : the journal of laboratory and clinical medicine, 2017-04, Vol.182, p.14-26.e4

2017

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Expedient Synthesis of a 72-Membered Isoxazolino-β-ketoamide Library by a 2·3-Component Reaction

ACS combinatorial science, 2012-02, Vol.14 (2), p.85-88

2012

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Expedient Synthesis of a 72-Membered Isoxazolino- beta -ketoamide Library by a 2.3-Component Reaction

ACS combinatorial science, 2012-02, Vol.14 (2), p.85-88-85-88

2012

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