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The Nitrosocarbonyl Hetero-Diels-Alder Reaction as a Useful Tool for Organic Syntheses

Angewandte Chemie (International ed.), 2011-06, Vol.50 (25), p.5630-5647

International ed. in English, 2011

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Nitroso Diels-Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products

Organic & biomolecular chemistry, 2014-10, Vol.12 (38), p.7445-7468

2014

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Iron Transport-Mediated Drug Delivery: Practical Syntheses and In Vitro Antibacterial Studies of Tris-Catecholate Siderophore–Aminopenicillin Conjugates Reveals Selectively Potent Antipseudomonal Activity

Journal of the American Chemical Society, 2012-06, Vol.134 (24), p.9898-9901

2012

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A dual read-out assay to evaluate the potency of compounds active against Mycobacterium tuberculosis

PloS one, 2013-04, Vol.8 (4), p.e60531

2013

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Antibacterials: Volume II

1, 2018

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Antibacterials: Volume I

1, 2018

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Targeting the Mycobacterium ulcerans cytochrome bc 1 :aa 3 for the treatment of Buruli ulcer

Nature communications, 2018-12, Vol.9 (1), p.1-9

2018

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Dual inhibition of the terminal oxidases eradicates antibiotic‐tolerant Mycobacterium tuberculosis

EMBO molecular medicine, 2021-01, Vol.13 (1), p.e13207-n/a

2021

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In Vivo Dearomatization of the Potent Antituberculosis Agent BTZ043 via Meisenheimer Complex Formation

Angewandte Chemie International Edition, 2017-02, Vol.56 (8), p.2187-2191

2017

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Bactericidal activity of an imidazo[1, 2-a]pyridine using a mouse M. tuberculosis infection model

PloS one, 2014-01, Vol.9 (1), p.e87483

2014

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Design and Syntheses of New Antibiotics Inspired by Nature’s Quest for Iron in an Oxidative Climate

Accounts of chemical research, 2021-04, Vol.54 (7), p.1646-1661

2021

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Stereo- and regioselectivity of the hetero-Diels-Alder reaction of nitroso derivatives with conjugated dienes

Beilstein journal of organic chemistry, 2016-09, Vol.12 (1), p.1949-1980

2016

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Intracellular and in vivo evaluation of imidazo[2,1-b]thiazole-5-carboxamide anti-tuberculosis compounds

PloS one, 2020-01, Vol.15 (1), p.e0227224-e0227224

2020

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Structure–activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters

European journal of medicinal chemistry, 2010-05, Vol.45 (5), p.1703-1716

2010

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N–O Chemistry for Antibiotics: Discovery of N-Alkyl-N-(pyridin-2-yl)hydroxylamine Scaffolds as Selective Antibacterial Agents Using Nitroso Diels–Alder and Ene Chemistry

Journal of medicinal chemistry, 2011-10, Vol.54 (19), p.6843-6858

2011

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Improved in vitro potency of Clofazimine derivatives against Neisseria species

European journal of medicinal chemistry reports, 2024-08, Vol.11, p.100147, Article 100147

2024

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Studies at the ionizable position of cephalosporins and penicillins: hydroxamates as substitutes for the traditional carboxylate group

Journal of antibiotics, 2017-03, Vol.70 (3), p.292-296

2017

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Enzymatic Deprotection of the Cephalosporin 3′-Acetoxy Group Using Candida antarctica Lipase B

Journal of organic chemistry, 2010-02, Vol.75 (4), p.1289-1292

2010

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Titanocene(III) Chloride-Mediated Reductions of Oxazines, Hydroxamic Acids, and N-Hydroxy Carbamates

Journal of organic chemistry, 2009-01, Vol.74 (1), p.448-451

2009

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Preparation and Evaluation of Potent Pentafluorosulfanyl‐Substituted Anti‐Tuberculosis Compounds

ChemMedChem, 2017-07, Vol.12 (14), p.1108-1115

2017

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GaMF1.39's antibiotic efficacy and its enhanced antitubercular activity in combination with clofazimine, Telacebec, ND-011992, or TBAJ-876

Microbiology spectrum, 2023-12, Vol.11 (6), p.e0228223-e0228223

2023

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A Synthetic Dual Drug Sideromycin Induces Gram-Negative Bacteria To Commit Suicide with a Gram-Positive Antibiotic

Journal of medicinal chemistry, 2018-05, Vol.61 (9), p.3845-3854

2018

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Biscatecholate–Monohydroxamate Mixed Ligand Siderophore–Carbacephalosporin Conjugates are Selective Sideromycin Antibiotics that Target Acinetobacter baumannii

Journal of medicinal chemistry, 2013-05, Vol.56 (10), p.4044-4052

2013

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Syntheses and Structure-Activity Relationships of N -Phenethyl-Quinazolin-4-yl-Amines as Potent Inhibitors of Cytochrome bd Oxidase in Mycobacterium tuberculosis

Applied sciences, 2021-10, Vol.11 (19), p.9092

2021

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Cyclopropanation of nitroso Diels–Alder cycloadducts and application to the synthesis of a 2′,3′-methano carbocyclic nucleoside

Tetrahedron letters, 2010-07, Vol.51 (29), p.3789-3791

2010

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The Nitrosocarbonyl Hetero-Diels-Alder Reaction as a Useful Tool for Organic Syntheses

Nitroso Diels-Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products

Iron Transport-Mediated Drug Delivery: Practical Syntheses and In Vitro Antibacterial Studies of Tris-Catecholate Siderophore–Aminopenicillin Conjugates Reveals Selectively Potent Antipseudomonal Activity

A dual read-out assay to evaluate the potency of compounds active against Mycobacterium tuberculosis

Antibacterials: Volume II

Antibacterials: Volume I

Targeting the Mycobacterium ulcerans cytochrome bc 1 :aa 3 for the treatment of Buruli ulcer

Dual inhibition of the terminal oxidases eradicates antibiotic‐tolerant Mycobacterium tuberculosis

In Vivo Dearomatization of the Potent Antituberculosis Agent BTZ043 via Meisenheimer Complex Formation

Bactericidal activity of an imidazo[1, 2-a]pyridine using a mouse M. tuberculosis infection model

Design and Syntheses of New Antibiotics Inspired by Nature’s Quest for Iron in an Oxidative Climate

Stereo- and regioselectivity of the hetero-Diels-Alder reaction of nitroso derivatives with conjugated dienes

Intracellular and in vivo evaluation of imidazo[2,1-b]thiazole-5-carboxamide anti-tuberculosis compounds

Structure–activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters

N–O Chemistry for Antibiotics: Discovery of N-Alkyl-N-(pyridin-2-yl)hydroxylamine Scaffolds as Selective Antibacterial Agents Using Nitroso Diels–Alder and Ene Chemistry

Improved in vitro potency of Clofazimine derivatives against Neisseria species

Studies at the ionizable position of cephalosporins and penicillins: hydroxamates as substitutes for the traditional carboxylate group

Enzymatic Deprotection of the Cephalosporin 3′-Acetoxy Group Using Candida antarctica Lipase B

Titanocene(III) Chloride-Mediated Reductions of Oxazines, Hydroxamic Acids, and N-Hydroxy Carbamates

Preparation and Evaluation of Potent Pentafluorosulfanyl‐Substituted Anti‐Tuberculosis Compounds

GaMF1.39's antibiotic efficacy and its enhanced antitubercular activity in combination with clofazimine, Telacebec, ND-011992, or TBAJ-876

A Synthetic Dual Drug Sideromycin Induces Gram-Negative Bacteria To Commit Suicide with a Gram-Positive Antibiotic

Biscatecholate–Monohydroxamate Mixed Ligand Siderophore–Carbacephalosporin Conjugates are Selective Sideromycin Antibiotics that Target Acinetobacter baumannii

Syntheses and Structure-Activity Relationships of N -Phenethyl-Quinazolin-4-yl-Amines as Potent Inhibitors of Cytochrome bd Oxidase in Mycobacterium tuberculosis

Cyclopropanation of nitroso Diels–Alder cycloadducts and application to the synthesis of a 2′,3′-methano carbocyclic nucleoside

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