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Chemistry

D-Index
46
Citations
8050
World Ranking
16017
National Ranking
695

Overview

Robert H. Dodd is affiliated with the Centre national de la recherche scientifique (CNRS) in France. Their research primarily focuses on materials science and chemistry, with a significant emphasis on materials chemistry and organic chemistry. Additional areas of study encompass neurology, molecular medicine, and ophthalmology.

Their scientific contributions span several key topics in their fields of study, including:

  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Synthesis and Catalytic Reactions
  • Neurosurgical Procedures and Complications
  • Carbohydrate Chemistry and Synthesis
  • Click Chemistry and Applications
  • Antibiotic Resistance in Bacteria

Dodd has published frequently in several venues, notably:

  • The Cambridge Structural Database (12 publications)
  • European Journal of Medicinal Chemistry (2 publications)
  • Frontiers in Ophthalmology (1 publication)
  • Bioorganic & Medicinal Chemistry Letters (1 publication)
  • Advanced Synthesis & Catalysis (1 publication)

They have collaborated repeatedly with coauthors including Pascal Retailleau (14 collaborations), Maurício Frota Saraiva (7 collaborations), Kevin Cariou (5 collaborations), Eugénie Romero (4 collaborations), and Agathe C. A. D'Hollander (4 collaborations).

Notable recent publications cover a range of topics, such as medicinal chemistry, neurology, and synthetic chemistry:

  • "Azetidinimines as a novel series of non-covalent broad-spectrum inhibitors of β-lactamases with submicromolar activities against carbapenemases KPC-2 (class A), NDM-1 (class B) and OXA-48 (class D)" (2021), European Journal of Medicinal Chemistry
  • "Improved Ophthalmic Outcomes Following Venous Sinus Stenting in Idiopathic Intracranial Hypertension" (2022), Frontiers in Ophthalmology
  • "EGCG-like non-competitive inhibitor of DYRK1A rescues cognitive defect in a down syndrome model" (2024), European Journal of Medicinal Chemistry
  • "Synthesis of tetracyclic oxindoles and evaluation of their α-glucosidase inhibitory and glucose consumption-promoting activity" (2020), Bioorganic & Medicinal Chemistry Letters
  • "Base-Mediated Generation of Ketenimines from Ynamides: [3+2] Annulation with Azaallyl Anions" (2021), Advanced Synthesis & Catalysis

Best Publications

  • Catalytic C-H amination: recent progress and future directions.

    Florence Collet;Robert H. Dodd;Philippe Dauban

  • Toward a Synthetically Useful Stereoselective C−H Amination of Hydrocarbons

    Chungen Liang;Florence Collet;Fabien Robert-Peillard;Paul Muller

  • Copper-catalyzed nitrogen transfer mediated by iodosylbenzene PhI=O.

    Philippe Dauban;Laurent Sanière;and Aurélie Tarrade;Robert H. Dodd

  • Efficient diastereoselective intermolecular rhodium-catalyzed C-H amination.

    Chungen Liang;Fabien Robert-Peillard;Corinne Fruit;Paul Müller

  • Iminoiodanes and C-NBond Formation in Organic Synthesis

    Philippe Dauban;Robert H. Dodd

  • Positive and negative allosteric modulators of the Ca2+-sensing receptor interact within overlapping but not identical binding sites in the transmembrane domain.

    Christophe Petrel;Albane Kessler;Philippe Dauban;Robert H. Dodd

  • Anxiogenic effects of methyl-β-carboline-3-carboxylate in a light/dark choice situation

    Catherine Belzung;René Misslin;Elise Vogel;Robert H. Dodd

  • PTH-independent regulation of blood calcium concentration by the calcium-sensing receptor.

    Alexandre Loupy;Suresh Krishna Ramakrishnan;Bharath Wootla;Régine Chambrey

  • Synthesis of Cyclic Sulfonamides via Intramolecular Copper-Catalyzed Reaction of Unsaturated Iminoiodinanes

    and Philippe Dauban;Robert H. Dodd

  • Evidence in Favor of a Calcium-Sensing Receptor in Arterial Endothelial Cells: Studies With Calindol and Calhex 231

    Arthur H. Weston;Mais Absi;Donald T. Ward;Jacqueline Ohanian

  • Modeling and Mutagenesis of the Binding Site of Calhex 231, a Novel Negative Allosteric Modulator of the Extracellular Ca2+-sensing Receptor

    Christophe Petrel;Albane Kessler;Fouzia Maslah;Philippe Dauban

  • PhINSes: A New Iminoiodinane Reagent for the Copper-Catalyzed Aziridination of Olefins

    Philippe Dauban;Robert H. Dodd

  • Intramolecular PhIO Mediated Copper-Catalyzed Aziridination of Unsaturated Sulfamates: A New Direct Access to Polysubstituted Amines from Simple Homoallylic Alcohols

    Fernando Javier Duran;Loïc Leman;Alberto Antonio Ghini;Gerardo Burton

  • Ketenimines Generated from Ynamides: Versatile Building Blocks for Nitrogen-Containing Scaffolds

    Robert H. Dodd;Kevin Cariou

  • Stereoselective rhodium-catalyzed imination of sulfides.

    Florence Collet;Robert H. Dodd;Philippe Dauban

  • Catalytic Oxyamidation of Indoles

    Stéphane Beaumont;Valérie Pons;Pascal Retailleau;Robert H. Dodd

  • Sulfonimidamides: efficient chiral iminoiodane precursors for diastereoselective copper-catalyzed aziridination of olefins.

    Pablo H Di Chenna;Fabien Robert-Peillard;Philippe Dauban;Robert H Dodd

  • Recent Progress in Iminoiodane-Mediated Aziridination of Olefins

    Delphine Karila;Robert H. Dodd

  • Design and synthesis of cyclic sulfonamides and sulfamates as new calcium sensing receptor agonists.

    Lionel Kiefer;Tatiana Gorojankina;Philippe Dauban;Hélène Faure

  • N2-benzyl-N1-(1-(1-naphthyl)ethyl)-3-phenylpropane-1,2-diamines and conformationally restrained indole analogues: development of calindol as a new calcimimetic acting at the calcium sensing receptor.

    Albane Kessler;Hélène Faure;Christophe Petrel;Martial Ruat

Frequent Co-Authors

Philippe Dauban
Philippe Dauban Institut de Chimie des Substances Naturelles
Pierre Potier
Pierre Potier Institut de Chimie des Substances Naturelles
Martial Ruat
Martial Ruat Centre national de la recherche scientifique, CNRS
Pascal Retailleau
Pascal Retailleau Centre national de la recherche scientifique, CNRS
Jean Rossier
Jean Rossier Sorbonne University
Werner Sieghart
Werner Sieghart Medical University of Vienna
Erwin Sigel
Erwin Sigel University of Bern
Didier Rognan
Didier Rognan University of Strasbourg
Thierry Naas
Thierry Naas University of Paris-Saclay
Yann Herault
Yann Herault Institute of Genetics and Molecular and Cellular Biology

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