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Rational Design, Synthesis, and Evaluation of Tetrahydroxamic Acid Chelators for Stable Complexation of Zirconium(IV)

Chemistry : a European journal, 2014-05, Vol.20 (19), p.5584-5591

2014

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Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts

Chemistry : a European journal, 2016-08, Vol.22 (35), p.12332-12339

2016

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Origin of the Isomer Stability of Polymethylated DOTA Chelates Complexed with Ln3+ Ions

European journal of inorganic chemistry, 2021-04, Vol.2021 (15), p.1428-1440

2021

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Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms

Chemistry : a European journal, 2017-03, Vol.23 (18), p.4353-4363

2017

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Analysis of the isomer ratios of polymethylated-DOTA complexes and the implications on protein structural studies

Dalton transactions : an international journal of inorganic chemistry, 2016-01, Vol.45 (11), p.4673-4687

2016

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Navigation of automated guided vehicles using magnet spot guidance method

Robotics and computer-integrated manufacturing, 2012-06, Vol.28 (3), p.425-436

2012

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The Intriguing Effects of Substituents in the N -Phenethyl Moiety of Norhydromorphone: A Bifunctional Opioid from a Set of "Tail Wags Dog" Experiments

Molecules (Basel, Switzerland), 2020-06, Vol.25 (11), p.2640

2020

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G-Protein biased opioid agonists: 3-hydroxy- N -phenethyl-5-phenylmorphans with three-carbon chain substituents at C9

RSC medicinal chemistry, 2020-08, Vol.11 (8), p.896-904

2020

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Cover Picture: Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts (Chem. Eur. J. 35/2016)

Chemistry : a European journal, 2016-08, Vol.22 (35), p.12201-12201

2016

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Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts

Chemistry : a European journal, 2016-08, Vol.22 (35), p.12205-12205

2016

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Conformational Structure and Energetics of 2-Methylphenyl(2′-methoxyphenyl)iodonium Chloride: Evidence for Solution Clusters

Chemistry : a European journal, 2010-09, Vol.16 (34), p.10418-10423

2010

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Cannabinoformins: Designing Biguanide-Embedded, Orally Available, Peripherally Selective Cannabinoid‑1 Receptor Antagonists for Metabolic Syndrome Disorders

Journal of medicinal chemistry, 2023-09, Vol.66 (17), p.11985-12004

2023

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Reply to the ‘Comment on “Investigation of Zr(iv) and 89Zr(iv) complexation with hydroxamates: progress towards designing a better chelator than desferrioxamine B for immuno-PET imaging”’ by A. Bianchi and M. Savastano, Chem. Commun., 2020, 56, D0CC01189D

Chemical communications (Cambridge, England), 2020-10, Vol.56 (83), p.12667-12668

2020

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Fast and High-Yield Microreactor Syntheses of ortho-Substituted [18F]Fluoroarenes from Reactions of [18F]Fluoride Ion with Diaryliodonium Salts

Journal of organic chemistry, 2010-05, Vol.75 (10), p.3332-3338

2010

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Origin of the Isomer Stability of Polymethylated DOTA Chelates Complexed with Ln 3+ ions

European journal of inorganic chemistry, 2021-04, Vol.2021 (15), p.1428-1440

2021

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The rules of attraction

Nature (London), 2003-09, Vol.425 (6956), p.357-359

2003

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A Toxoplasma gondii O-glycosyltransferase that modulates bradyzoite cyst wall rigidity is distinct from host homologues

Nature communications, 2024-05, Vol.15 (1), p.3792-3792, Article 3792

2024

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Dynamics of Proton Transfer in Bacteriorhodopsin

Journal of the American Chemical Society, 2004-02, Vol.126 (7), p.2225-2230

2004

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Synthesis, Biological Evaluation, and Molecular Modeling Studies of 3,4-Diarylpyrazoline Series of Compounds as Potent, Nonbrain Penetrant Antagonists of Cannabinoid‑1 (CB1R) Receptor with Reduced Lipophilicity

Journal of medicinal chemistry, 2022-02, Vol.65 (3), p.2374-2387

2022

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An Investigation of (Diacetoxyiodo)arenes as Precursors for Preparing No-Carrier-Added [18F]Fluoroarenes from Cyclotron-Produced [18F]Fluoride Ion

Journal of organic chemistry, 2016-01, Vol.81 (1), p.297-302

2016

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Substrate specificity of the deazaflavin‐dependent nitroreductase from Mycobacterium tuberculosis responsible for the bioreductive activation of bicyclic nitroimidazoles

The FEBS journal, 2012-01, Vol.279 (1), p.113-125

2012

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Structure of Ddn, the Deazaflavin-Dependent Nitroreductase from Mycobacterium tuberculosis Involved in Bioreductive Activation of PA-824

Structure (London), 2012-01, Vol.20 (1), p.101-112

2012

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Structural Basis of Species-Dependent Differential Affinity of 6-Alkoxy-5-Aryl-3-Pyridinecarboxamide Cannabinoid-1 Receptor Antagonists

Molecular pharmacology, 2015-08, Vol.88 (2), p.238-244

2015

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Modulation of opioid receptor affinity and efficacy via N-substitution of 9β-hydroxy-5-(3-hydroxyphenyl)morphan: Synthesis and computer simulation study

Bioorganic & medicinal chemistry, 2017-04, Vol.25 (8), p.2406-2422

2017

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Synthesis and evaluation of two new candidate high-affinity full agonist PET radioligands for imaging 5-HT1B receptors

Nuclear medicine and biology, 2019-03, Vol.70, p.1-13

2019

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Rational Design, Synthesis, and Evaluation of Tetrahydroxamic Acid Chelators for Stable Complexation of Zirconium(IV)

Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts

Origin of the Isomer Stability of Polymethylated DOTA Chelates Complexed with Ln3+ Ions

Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms

Analysis of the isomer ratios of polymethylated-DOTA complexes and the implications on protein structural studies

Navigation of automated guided vehicles using magnet spot guidance method

The Intriguing Effects of Substituents in the N -Phenethyl Moiety of Norhydromorphone: A Bifunctional Opioid from a Set of "Tail Wags Dog" Experiments

G-Protein biased opioid agonists: 3-hydroxy- N -phenethyl-5-phenylmorphans with three-carbon chain substituents at C9

Cover Picture: Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts (Chem. Eur. J. 35/2016)

Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts

Conformational Structure and Energetics of 2-Methylphenyl(2′-methoxyphenyl)iodonium Chloride: Evidence for Solution Clusters

Cannabinoformins: Designing Biguanide-Embedded, Orally Available, Peripherally Selective Cannabinoid‑1 Receptor Antagonists for Metabolic Syndrome Disorders

Reply to the ‘Comment on “Investigation of Zr(iv) and 89Zr(iv) complexation with hydroxamates: progress towards designing a better chelator than desferrioxamine B for immuno-PET imaging”’ by A. Bianchi and M. Savastano, Chem. Commun., 2020, 56, D0CC01189D

Fast and High-Yield Microreactor Syntheses of ortho-Substituted [18F]Fluoroarenes from Reactions of [18F]Fluoride Ion with Diaryliodonium Salts

Origin of the Isomer Stability of Polymethylated DOTA Chelates Complexed with Ln 3+ ions

The rules of attraction

A Toxoplasma gondii O-glycosyltransferase that modulates bradyzoite cyst wall rigidity is distinct from host homologues

Dynamics of Proton Transfer in Bacteriorhodopsin

Synthesis, Biological Evaluation, and Molecular Modeling Studies of 3,4-Diarylpyrazoline Series of Compounds as Potent, Nonbrain Penetrant Antagonists of Cannabinoid‑1 (CB1R) Receptor with Reduced Lipophilicity

An Investigation of (Diacetoxyiodo)arenes as Precursors for Preparing No-Carrier-Added [18F]Fluoroarenes from Cyclotron-Produced [18F]Fluoride Ion

Substrate specificity of the deazaflavin‐dependent nitroreductase from Mycobacterium tuberculosis responsible for the bioreductive activation of bicyclic nitroimidazoles

Structure of Ddn, the Deazaflavin-Dependent Nitroreductase from Mycobacterium tuberculosis Involved in Bioreductive Activation of PA-824

Structural Basis of Species-Dependent Differential Affinity of 6-Alkoxy-5-Aryl-3-Pyridinecarboxamide Cannabinoid-1 Receptor Antagonists

Modulation of opioid receptor affinity and efficacy via N-substitution of 9β-hydroxy-5-(3-hydroxyphenyl)morphan: Synthesis and computer simulation study

Synthesis and evaluation of two new candidate high-affinity full agonist PET radioligands for imaging 5-HT1B receptors

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