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Expedient syntheses of N-heterocycles via intermolecular amphoteric diamination of allenes

Nature communications, 2018-02, Vol.9 (1), p.721-11, Article 721

2018

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Assay of Ivermectin Including Determination and Identification of Its Related Substances in Ivermectin Injectable Product by a Stability-Indicating RP-HPLC Method

Chromatographia, 2021-11, Vol.84 (11), p.989-997

2021

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Two-step reaction mechanism reveals new antioxidant capability of cysteine disulfides against hydroxyl radical attack

Proceedings of the National Academy of Sciences - PNAS, 2020-08, Vol.117 (31), p.18216-18223

2020

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Reactivity of hydropersulfides toward the hydroxyl radical unraveled: disulfide bond cleavage, hydrogen atom transfer, and proton-coupled electron transfer

Physical chemistry chemical physics : PCCP, 2018, Vol.20 (7), p.4793-4804

2018

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Thiyl Radical-Based Charge Tagging Enables Sterol Quantitation via Mass Spectrometry

Analytical chemistry (Washington), 2017-12, Vol.89 (23), p.12631-12635

2017

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Acetone/Isopropanol Photoinitiating System Enables Tunable Disulfide Reduction and Disulfide Mapping via Tandem Mass Spectrometry

Analytical chemistry (Washington), 2018-11, Vol.90 (21), p.13036-13043

2018

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Simultaneous determination of ivermectin, clorsulon and their related substances in an injectable finished product by a stability-indicating RP-HPLC method

Journal of pharmaceutical and biomedical analysis, 2022-02, Vol.210, p.114580-114580, Article 114580

2022

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A comprehensive study to identify and characterize major degradation products of Ivermectin drug substance including its degradation pathways using LC-HRMS and NMR

Journal of pharmaceutical and biomedical analysis, 2022-05, Vol.214, p.114730-114730, Article 114730

2022

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Identification and characterization of major degradation products of Eprinomectin drug substance including degradation pathways using LC-HRMS and NMR

Journal of pharmaceutical and biomedical analysis, 2022-06, Vol.215, p.114767-114767, Article 114767

2022

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Structural elucidation of major degradation products of milbemycin oxime drug substance using LC-MS and NMR

Journal of pharmaceutical and biomedical analysis, 2022-08, Vol.217, p.114862-114862, Article 114862

2022

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Development of a Simple Extraction Procedure and an HPLC Method for the Determination of Delmopinol in a Challenging Rubbery Dental Chew

Journal of AOAC International, 2023-05, Vol.106 (3), p.778

2023

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Assay of afoxolaner and determination of its related substances in commercial bulk batches of afoxolaner by reversed-phase HPLC method based on a short octadecyl column

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2021-11, Vol.1184, p.122984-122984, Article 122984

2021

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Shotgun Analysis of Diacylglycerols Enabled by Thiol–ene Click Chemistry

Analytical chemistry (Washington), 2018-04, Vol.90 (8), p.5239-5246

2018

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Comprehensive study on degradation profile of firocoxib and structural elucidation of its key degradation products

Journal of pharmaceutical and biomedical analysis, 2023-02, Vol.224, p.115192-115192, Article 115192

2023

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Top-down analysis of disulfide-linked proteins using photoinduced radical reactions and ET-DDC

International journal of mass spectrometry, 2019-10, Vol.444, p.116173, Article 116173

2019

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Reactivity of hydropersulfides toward the hydroxyl radical unraveled: disulfide bond cleavage, hydrogen atom transfer, and proton-coupled electron transferElectronic supplementary information (ESI) available: The supplementary information contains a figure with the main geometrical parameters of the pre-reactive complexes of the HSSH + OH reaction, and tables including the relative energies of all reactions investigated, the absolute energies, the main topological parameters of selected transiti

2018-02

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Dipolar DC induced collisional activation of non‐dissociated electron‐transfer products

Journal of mass spectrometry., 2019-05, Vol.54 (5), p.459-465

2019

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Radical Chemistry and Mass Spectrometry for Enhanced Biomolecule Analysis

Adhikari, Sarju

2019

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Heptamolybdate: a highly active sulfide oxygenation catalystDedicated to Professor Kim Dunbar on the occasion of her 60th Birthday.Electronic supplementary information (ESI) available. CCDC 1839304. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8dt00583d

2018-08

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Heptamolybdate: a highly active sulfide oxygenation catalyst

Dalton transactions : an international journal of inorganic chemistry, 2018, Vol.47 (34), p.11882-11887

2018

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Palladium-catalyzed ortho-halogenation of diaryl oxime ethers

Tetrahedron letters, 2014-08, Vol.55 (34), p.4801-4806

2014

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Stereospecific Suzuki, Sonogashira, and Negishi Coupling Reactions of N‑Alkoxyimidoyl Iodides and Bromides

Journal of organic chemistry, 2013-04, Vol.78 (8), p.3676-3687

2013

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ChemInform Abstract: Palladium-Catalyzed ortho-Halogenation of Diaryl Oxime Ethers

ChemInform, 2015-01, Vol.46 (3), p.no-no

2015

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Expedient syntheses of N-heterocycles via intermolecular amphoteric diamination of allenes

Assay of Ivermectin Including Determination and Identification of Its Related Substances in Ivermectin Injectable Product by a Stability-Indicating RP-HPLC Method

Two-step reaction mechanism reveals new antioxidant capability of cysteine disulfides against hydroxyl radical attack

Reactivity of hydropersulfides toward the hydroxyl radical unraveled: disulfide bond cleavage, hydrogen atom transfer, and proton-coupled electron transfer

Thiyl Radical-Based Charge Tagging Enables Sterol Quantitation via Mass Spectrometry

Acetone/Isopropanol Photoinitiating System Enables Tunable Disulfide Reduction and Disulfide Mapping via Tandem Mass Spectrometry

Simultaneous determination of ivermectin, clorsulon and their related substances in an injectable finished product by a stability-indicating RP-HPLC method

A comprehensive study to identify and characterize major degradation products of Ivermectin drug substance including its degradation pathways using LC-HRMS and NMR

Identification and characterization of major degradation products of Eprinomectin drug substance including degradation pathways using LC-HRMS and NMR

Structural elucidation of major degradation products of milbemycin oxime drug substance using LC-MS and NMR

Development of a Simple Extraction Procedure and an HPLC Method for the Determination of Delmopinol in a Challenging Rubbery Dental Chew

Assay of afoxolaner and determination of its related substances in commercial bulk batches of afoxolaner by reversed-phase HPLC method based on a short octadecyl column

Shotgun Analysis of Diacylglycerols Enabled by Thiol–ene Click Chemistry

Comprehensive study on degradation profile of firocoxib and structural elucidation of its key degradation products

Top-down analysis of disulfide-linked proteins using photoinduced radical reactions and ET-DDC

Dipolar DC induced collisional activation of non‐dissociated electron‐transfer products

Radical Chemistry and Mass Spectrometry for Enhanced Biomolecule Analysis

Heptamolybdate: a highly active sulfide oxygenation catalystDedicated to Professor Kim Dunbar on the occasion of her 60th Birthday.Electronic supplementary information (ESI) available. CCDC 1839304. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8dt00583d

Heptamolybdate: a highly active sulfide oxygenation catalyst

Palladium-catalyzed ortho-halogenation of diaryl oxime ethers

Stereospecific Suzuki, Sonogashira, and Negishi Coupling Reactions of N‑Alkoxyimidoyl Iodides and Bromides

ChemInform Abstract: Palladium-Catalyzed ortho-Halogenation of Diaryl Oxime Ethers

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