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Carbenium ion formation by fragmentation of electrochemically generated oxonium ions

Organic & biomolecular chemistry, 2018, Vol.16 (28), p.5094-5096

2018

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Structure-based identification of salicylic acid derivatives as malarial threonyl tRNA-synthetase inhibitors

PloS one, 2024, Vol.19 (4), p.e0296995-e0296995

2024

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Synthesis of indazoles from 2-formylphenylboronic acids

RSC advances, 2021-06, Vol.11 (37), p.2271-22714

2021

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3-(Adenosylthio)benzoic Acid Derivatives as SARS-CoV-2 Nsp14 Methyltransferase Inhibitors

Molecules (Basel, Switzerland), 2023-01, Vol.28 (2), p.768

2023

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Intramolecular Friedel–Crafts alkylation by electrochemical carbenium ion generation

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2022-12, Vol.58 (12), p.732-736

2022

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Unsaturated syn- and anti-1,2-Amino Alcohols by Cyclization of Allylic Bis-trichloroacetimidates. Stereoselectivity Dependence on Substrate Configuration

Journal of organic chemistry, 2015-01, Vol.80 (2), p.920-927

2015

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Synthesis of Alkynyl-Glycinols by Lewis Acid Catalyzed Propargylic Substitution of Bis-Imidates

European journal of organic chemistry, 2015-11, Vol.2015 (31), p.6900-6908

2015

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Potent SARS-CoV‑2 mRNA Cap Methyltransferase Inhibitors by Bioisosteric Replacement of Methionine in SAM Cosubstrate

ACS medicinal chemistry letters, 2021-07, Vol.12 (7), p.1102-1107

2021

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Lewis Acid Catalyzed Intramolecular Allylic Substitution of Bis(trichloroacetimidates): A Versatile Approach to Racemic Unsaturated Amino Acids

European Journal of Organic Chemistry, 2011-05, Vol.2011 (13), p.2421-2425

2011

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Electrochemical Formation of Oxazolines by 1,3-Oxyfluorination of Non-activated Cyclopropanes

Organic letters, 2024-03, Vol.26 (11), p.2158-2162

2024

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Discovery of SARS-CoV-2 Nsp14 and Nsp16 Methyltransferase Inhibitors by High-Throughput Virtual Screening

Pharmaceuticals (Basel, Switzerland), 2021-11, Vol.14 (12), p.1243

2021

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Synthesis and SAR of phenylazoles, active against Staphylococcus aureus Newman

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2022-12, Vol.58 (12), p.737-748

2022

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Functionalization of Tetrazoles Bearing the Electrochemically Cleavable 1N‑(6-Methylpyridyl-2-methyl) Protecting Group

ACS omega, 2022-05, Vol.7 (21), p.18103-18109

2022

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Inhibition of O-acetylserine sulfhydrylase by fluoroalanine derivatives

Journal of enzyme inhibition and medicinal chemistry, 2018-01, Vol.33 (1), p.1343-1351

2018

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Functionalization of 1N‑Protected Tetrazoles by Deprotonation with the Turbo Grignard Reagent

Journal of organic chemistry, 2022-03, Vol.87 (5), p.3810-3816

2022

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Functionalization of 1 N -Protected Tetrazoles by Deprotonation with the Turbo Grignard Reagent

Journal of organic chemistry, 2022-03, Vol.87 (5), p.3810-3816

2022

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Synthesis of 2-aminopyridopyrimidinones and their plasmepsin I, II, IV inhibition potency

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2020-06, Vol.56 (6), p.786-792

2020

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Refining the structure−activity relationships of 2-phenylcyclopropane carboxylic acids as inhibitors of O-acetylserine sulfhydrylase isoforms

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.31-43

2019

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Friedel–Crafts Alkylation with Carbenium Ions Generated by Electrochemical Oxidation of Stannylmethyl Ethers

European journal of organic chemistry, 2020-08, Vol.2020 (29), p.4510-4516

2020

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Discovery of novel fragments inhibiting O-acetylserine sulphhydrylase by combining scaffold hopping and ligand-based drug design

Journal of enzyme inhibition and medicinal chemistry, 2018-01, Vol.33 (1), p.1444-1452

2018

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Catalytic Enantioselective Synthesis of 4-Vinyl-2-trichloromethyloxazoline: An Access to Enantioenriched Vinylglycinol Surrogate

Journal of organic chemistry, 2010-11, Vol.75 (22), p.7897-7900

2010

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Amide-Group-Directed Protonolysis of Cyclopropane: An Approach to 2,2-Disubstituted Pyrrolidines

Organic letters, 2017-05, Vol.19 (10), p.2478-2481

2017

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Exploiting Structural Dynamics To Design Open-Flap Inhibitors of Malarial Aspartic Proteases

Journal of medicinal chemistry, 2019-10, Vol.62 (20), p.8931-8950

2019

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Carbenium ion formation by fragmentation of electrochemically generated oxonium ionsElectronic supplementary information (ESI) available: Experimental details, cyclic voltammograms, and NMR data. See DOI: 10.1039/c8ob01339j

2018-07

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Synthesis of α-Ethynyl Glycines

European journal of organic chemistry, 2016-09, Vol.2016 (27), p.4591-4602

2016

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Carbenium ion formation by fragmentation of electrochemically generated oxonium ions

Structure-based identification of salicylic acid derivatives as malarial threonyl tRNA-synthetase inhibitors

Synthesis of indazoles from 2-formylphenylboronic acids

3-(Adenosylthio)benzoic Acid Derivatives as SARS-CoV-2 Nsp14 Methyltransferase Inhibitors

Intramolecular Friedel–Crafts alkylation by electrochemical carbenium ion generation

Unsaturated syn- and anti-1,2-Amino Alcohols by Cyclization of Allylic Bis-trichloroacetimidates. Stereoselectivity Dependence on Substrate Configuration

Synthesis of Alkynyl-Glycinols by Lewis Acid Catalyzed Propargylic Substitution of Bis-Imidates

Potent SARS-CoV‑2 mRNA Cap Methyltransferase Inhibitors by Bioisosteric Replacement of Methionine in SAM Cosubstrate

Lewis Acid Catalyzed Intramolecular Allylic Substitution of Bis(trichloroacetimidates): A Versatile Approach to Racemic Unsaturated Amino Acids

Electrochemical Formation of Oxazolines by 1,3-Oxyfluorination of Non-activated Cyclopropanes

Discovery of SARS-CoV-2 Nsp14 and Nsp16 Methyltransferase Inhibitors by High-Throughput Virtual Screening

Synthesis and SAR of phenylazoles, active against Staphylococcus aureus Newman

Functionalization of Tetrazoles Bearing the Electrochemically Cleavable 1N‑(6-Methylpyridyl-2-methyl) Protecting Group

Inhibition of O-acetylserine sulfhydrylase by fluoroalanine derivatives

Functionalization of 1N‑Protected Tetrazoles by Deprotonation with the Turbo Grignard Reagent

Functionalization of 1 N -Protected Tetrazoles by Deprotonation with the Turbo Grignard Reagent

Synthesis of 2-aminopyridopyrimidinones and their plasmepsin I, II, IV inhibition potency

Refining the structure−activity relationships of 2-phenylcyclopropane carboxylic acids as inhibitors of O-acetylserine sulfhydrylase isoforms

Friedel–Crafts Alkylation with Carbenium Ions Generated by Electrochemical Oxidation of Stannylmethyl Ethers

Discovery of novel fragments inhibiting O-acetylserine sulphhydrylase by combining scaffold hopping and ligand-based drug design

Catalytic Enantioselective Synthesis of 4-Vinyl-2-trichloromethyloxazoline: An Access to Enantioenriched Vinylglycinol Surrogate

Amide-Group-Directed Protonolysis of Cyclopropane: An Approach to 2,2-Disubstituted Pyrrolidines

Exploiting Structural Dynamics To Design Open-Flap Inhibitors of Malarial Aspartic Proteases

Carbenium ion formation by fragmentation of electrochemically generated oxonium ionsElectronic supplementary information (ESI) available: Experimental details, cyclic voltammograms, and NMR data. See DOI: 10.1039/c8ob01339j

Synthesis of α-Ethynyl Glycines

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