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Benjamin P Vokits

Showing results (1-10 of 7) with videos related to

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Journal of the American Chemical Society|December 30, 2025
Decoding the Nested, Multicycle Mechanism of Ni-Catalyzed Redox-Neutral Cross-Coupling through Temperature Scanning Reaction CalorimetryDavid A Cagan, Áron Péter, Benjamin P Vokits, et al.
Science (New York, N.Y.)|March 6, 2025
Sulfonyl hydrazides as a general redox-neutral platform for radical cross-couplingJiawei Sun, Áron Péter, Jiayan He, et al.
Bioorganic & Medicinal Chemistry|October 2, 2020
Discovery and structure activity relationships of 7-benzyl triazolopyridines as stable, selective, and reversible inhibitors of myeloperoxidaseScott A Shaw, Benjamin P Vokits, Andrew K Dilger, et al.
Medchemcomm|August 16, 2018
Triazolopyrimidines identified as reversible myeloperoxidase inhibitorsFranck Duclos, Lynn M Abell, David G Harden, et al.
Bioorganic & Medicinal Chemistry Letters|February 5, 2013
Discovery of (1R,2R)-N-(4-(6-isopropylpyridin-2-yl)-3-(2-methyl-2H-indazol-5-yl)isothiazol-5-yl)-2-methylcyclopropanecarboxamide, a potent and orally efficacious mGlu5 receptor negative allosteric modulatorJunliang Hao, Veronique Dehlinger, Adam M Fivush, et al.
The Journal of Organic Chemistry|July 8, 2015
Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte DevelopmentScott A Shaw, Balu Balasubramanian, Samuel Bonacorsi, et al.
The Journal of Organic Chemistry|September 3, 2015
Correction to "Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte Development"Scott A Shaw, Balu Balasubramanian, Samuel Bonacorsi, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of the American Chemical Society|December 30, 2025
Decoding the Nested, Multicycle Mechanism of Ni-Catalyzed Redox-Neutral Cross-Coupling through Temperature Scanning Reaction CalorimetryDavid A Cagan, Áron Péter, Benjamin P Vokits, et al.
Science (New York, N.Y.)|March 6, 2025
Sulfonyl hydrazides as a general redox-neutral platform for radical cross-couplingJiawei Sun, Áron Péter, Jiayan He, et al.
Bioorganic & Medicinal Chemistry|October 2, 2020
Discovery and structure activity relationships of 7-benzyl triazolopyridines as stable, selective, and reversible inhibitors of myeloperoxidaseScott A Shaw, Benjamin P Vokits, Andrew K Dilger, et al.
Medchemcomm|August 16, 2018
Triazolopyrimidines identified as reversible myeloperoxidase inhibitorsFranck Duclos, Lynn M Abell, David G Harden, et al.
Bioorganic & Medicinal Chemistry Letters|February 5, 2013
Discovery of (1R,2R)-N-(4-(6-isopropylpyridin-2-yl)-3-(2-methyl-2H-indazol-5-yl)isothiazol-5-yl)-2-methylcyclopropanecarboxamide, a potent and orally efficacious mGlu5 receptor negative allosteric modulatorJunliang Hao, Veronique Dehlinger, Adam M Fivush, et al.
The Journal of Organic Chemistry|July 8, 2015
Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte DevelopmentScott A Shaw, Balu Balasubramanian, Samuel Bonacorsi, et al.
The Journal of Organic Chemistry|September 3, 2015
Correction to "Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte Development"Scott A Shaw, Balu Balasubramanian, Samuel Bonacorsi, et al.
Pageof 1