World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
47
Citations
8056
World Ranking
15637
National Ranking
678

Philippe Dauban publication distribution in Chemistry in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Chemistry in 2026. The highlighted bar marks where Philippe Dauban sits on this spectrum.

61–80 publications: 66 scientists 81–100 publications: 302 scientists 101–120 publications: 623 scientists 121–140 publications: 918 scientists 141–160 publications: 1,218 scientists 161–180 publications: 1,350 scientists 181–200 publications: 1,344 scientists 201–220 publications: 1,281 scientists 221–240 publications: 1,216 scientists 241–260 publications: 1,100 scientists 261–280 publications: 979 scientists 281–300 publications: 939 scientists 301–320 publications: 764 scientists 321–340 publications: 643 scientists 341–360 publications: 628 scientists 361–380 publications: 522 scientists 381–400 publications: 459 scientists 401–420 publications: 397 scientists 421–440 publications: 327 scientists 441–460 publications: 270 scientists 461–480 publications: 265 scientists 481–500 publications: 252 scientists 501–520 publications: 201 scientists 521–540 publications: 185 scientists 541–560 publications: 148 scientists 561–580 publications: 148 scientists 581–600 publications: 132 scientists 601–620 publications: 114 scientists 621–640 publications: 104 scientists 641–660 publications: 91 scientists 661–680 publications: 92 scientists 681–700 publications: 73 scientists 701–720 publications: 57 scientists 721–740 publications: 54 scientists 741–760 publications: 67 scientists 761–780 publications: 45 scientists 781–800 publications: 46 scientists 801–820 publications: 39 scientists 821–840 publications: 32 scientists 841–860 publications: 36 scientists 861–880 publications: 29 scientists 881–900 publications: 26 scientists 901–920 publications: 24 scientists 921–940 publications: 14 scientists 941–960 publications: 23 scientists 961–980 publications: 28 scientists 981–1,000 publications: 15 scientists 1,001–1,020 publications: 29 scientists 1,021–1,040 publications: 12 scientists 1,041–1,060 publications: 19 scientists 1,061–1,080 publications: 12 scientists 1,081–1,100 publications: 6 scientists 1,101–1,120 publications: 8 scientists 1,121–1,140 publications: 12 scientists 1,141–1,160 publications: 5 scientists 1,161–1,180 publications: 6 scientists 1,181–1,200 publications: 14 scientists 1,201–1,220 publications: 7 scientists 1,221–1,240 publications: 2 scientists 1,241–1,260 publications: 6 scientists 1,261–1,280 publications: 4 scientists 1,281–1,294 publications: 6 scientists 1,295+ publications: 100 scientists
61 publications 1,295+

This scientist: 139 publications — 10th percentile

10% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 1,295 publications or more.

Philippe Dauban D-index placement in Chemistry in 2026

The chart shows the D-index (discipline H-index) distribution of Chemistry scientists ranked by Research.com in 2026. The highlighted bar marks where Philippe Dauban sits on this spectrum.

40–41 D-Index: 289 scientists 42–43 D-Index: 612 scientists 44–45 D-Index: 808 scientists 46–47 D-Index: 776 scientists 48–49 D-Index: 835 scientists 50–51 D-Index: 861 scientists 52–53 D-Index: 872 scientists 54–55 D-Index: 933 scientists 56–57 D-Index: 1,051 scientists 58–59 D-Index: 930 scientists 60–61 D-Index: 882 scientists 62–63 D-Index: 834 scientists 64–65 D-Index: 731 scientists 66–67 D-Index: 775 scientists 68–69 D-Index: 683 scientists 70–71 D-Index: 646 scientists 72–73 D-Index: 561 scientists 74–75 D-Index: 501 scientists 76–77 D-Index: 437 scientists 78–79 D-Index: 388 scientists 80–81 D-Index: 354 scientists 82–83 D-Index: 292 scientists 84–85 D-Index: 275 scientists 86–87 D-Index: 254 scientists 88–89 D-Index: 235 scientists 90–91 D-Index: 185 scientists 92–93 D-Index: 192 scientists 94–95 D-Index: 155 scientists 96–97 D-Index: 163 scientists 98–99 D-Index: 125 scientists 100–101 D-Index: 105 scientists 102–103 D-Index: 105 scientists 104–105 D-Index: 112 scientists 106–107 D-Index: 88 scientists 108–109 D-Index: 68 scientists 110–111 D-Index: 69 scientists 112–113 D-Index: 65 scientists 114–115 D-Index: 79 scientists 116–117 D-Index: 61 scientists 118–119 D-Index: 44 scientists 120–121 D-Index: 37 scientists 122–123 D-Index: 40 scientists 124–125 D-Index: 33 scientists 126–127 D-Index: 26 scientists 128–129 D-Index: 34 scientists 130–131 D-Index: 35 scientists 132–133 D-Index: 25 scientists 134–135 D-Index: 27 scientists 136–137 D-Index: 17 scientists 138–139 D-Index: 16 scientists 140–141 D-Index: 20 scientists 142–143 D-Index: 20 scientists 144–145 D-Index: 15 scientists 146–147 D-Index: 9 scientists 148–149 D-Index: 9 scientists 150–151 D-Index: 16 scientists 152–153 D-Index: 11 scientists 154–155 D-Index: 9 scientists 156–157 D-Index: 3 scientists 158 D-Index: 3 scientists 159+ D-Index: 98 scientists
40 D-Index 159+

This scientist: 47 D-Index — 14th percentile

14% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 159 D-Index or more.

Overview

Philippe Dauban is affiliated with the Institut de Chimie des Substances Naturelles in France. Their research is primarily situated within the fields of chemistry and materials science, with a strong focus on organic chemistry and materials chemistry as subfields.

Their scholarly output covers a range of topics related to catalysis, synthesis, and crystallography. Key topics addressed in their work include:

  • Catalytic C-H Functionalization Methods
  • Synthesis and Catalytic Reactions
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Cyclopropane Reaction Mechanisms
  • Asymmetric Hydrogenation and Catalysis
  • Sulfur-Based Synthesis Techniques

Dauban's recent papers illustrate a strong emphasis on catalytic and asymmetric synthesis methods, with a focus on C(sp3)-H amination and intermolecular functionalization processes. Selected recent publications include:

  • "Catalytic Intermolecular C(sp3)-H Amination: Selective Functionalization of Tertiary C-H Bonds vs Activated Benzylic C-H Bonds" (2021), Journal of the American Chemical Society
  • "Rhodium(II)-Catalyzed Enantioselective Intermolecular Aziridination of Alkenes" (2022), Journal of the American Chemical Society
  • "Asymmetric Intramolecular Buchner Reaction: From High Stereoselectivity to Coexistence of Norcaradiene, Cycloheptatriene, and an Intermediate Form in the Solid State" (2021), Organic Letters
  • "Catalyst-Controlled Intermolecular Homobenzylic C(sp3)-H Amination for the Synthesis of β-Arylethylamines" (2024), Journal of the American Chemical Society
  • "Asymmetric Synthesis of Enantiopure Pyrrolidines by C(sp3)−H Amination of Hydrocarbons" (2021), Angewandte Chemie International Edition

Dauban frequently publishes in several scientific venues, including:

  • The Cambridge Structural Database
  • European Journal of Organic Chemistry
  • Journal of the American Chemical Society
  • Organic Letters
  • Angewandte Chemie International Edition

The scientist collaborates regularly with a group of frequent coauthors, such as:

  • Tanguy Saget
  • Benjamin Darses
  • Erwan Brunard
  • Vincent Boquet
  • Pascal Retailleau

Best Publications

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

    Florence Collet;Robert H. Dodd;Philippe Dauban

  • Catalytic C–H amination: the stereoselectivity issue

    Florence Collet;Camille Lescot;Philippe Dauban

  • Nitrene Chemistry in Organic Synthesis: Still in Its Infancy?

    Geoffroy Dequirez;Valérie Pons;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

  • Transition metal-catalyzed iodine( iii )-mediated nitrene transfer reactions: efficient tools for challenging syntheses

    B. Darses;R. Rodrigues;L. Neuville;M. Mazurais

  • 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

  • A Masked 1,3‐Dipole Revealed from Aziridines

    Philippe Dauban;Guillaume Malik

  • 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

  • Nitren‐Chemie in der organischen Synthese: noch in den Kinderschuhen?

    Geoffroy Dequirez;Valérie Pons;Philippe Dauban

  • 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

  • Studies in catalytic C-H amination involving nitrene C-H insertion.

    Florence Collet;Camille Lescot;Chungen Liang;Philippe Dauban

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

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

Robert H. Dodd
Robert H. Dodd Centre national de la recherche scientifique, CNRS
Martial Ruat
Martial Ruat Centre national de la recherche scientifique, CNRS
Pascal Retailleau
Pascal Retailleau Centre national de la recherche scientifique, CNRS
Pierre Potier
Pierre Potier Institut de Chimie des Substances Naturelles
Vincent Gandon
Vincent Gandon University of Paris-Saclay
Didier Rognan
Didier Rognan University of Strasbourg
Jean-Philippe Pin
Jean-Philippe Pin University of Montpellier
M. Mar Díaz-Requejo
M. Mar Díaz-Requejo University of Huelva
Paul Müller
Paul Müller University of Geneva
Laurent Prézeau
Laurent Prézeau University of Montpellier

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