World's Best Scientists 2026 revealed!
Gérald Guillaumet

Gérald Guillaumet

D-Index & Metrics

Chemistry

D-Index
44
Citations
8919
World Ranking
16697
National Ranking
732

Gérald Guillaumet 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 Gérald Guillaumet 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: 570 publications — 92nd percentile

92% of scientists in this discipline score the same or lower.

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

Gérald Guillaumet 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 Gérald Guillaumet 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: 44 D-Index — 7th percentile

7% of scientists in this discipline score the same or lower.

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

Overview

Gérald Guillaumet is affiliated with the University of Orléans in France and has contributed extensively to the field of Chemistry, particularly focusing on Organic Chemistry. Their research encompasses multiple subfields, including Molecular Biology, Materials Chemistry, Physiology, and Infectious Diseases, reflecting a multidisciplinary approach to chemical science.

The scientist's primary research interests include Catalytic C-H Functionalization Methods, Synthesis and biological activity, Catalytic Cross-Coupling Reactions, Synthesis and Biological Evaluation, Synthesis and Catalytic Reactions, Synthesis and Characterization of Heterocyclic Compounds, and Sulfur-Based Synthesis Techniques.

Notable recent publications by Gérald Guillaumet include:

  • Synthesis, Anticancer Activities and Molecular Docking Studies of a Novel Class of 2-Phenyl-5,6,7,8-tetrahydroimidazo [1,2-b]pyridazine Derivatives Bearing Sulfonamides (2022, Molecules)
  • Efficient microwave-assisted Suzuki-Miyaura cross-coupling reaction of 3-bromo pyrazolo[1,5-a]pyrimidin-5(4H)-one: towards a new access to 3,5-diarylated 7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine derivatives (2021, RSC Advances)
  • "On Water" Palladium Catalyzed Direct Arylation of 1H-Indazole and 1H-7-Azaindazole (2020, Molecules)
  • Synthesis and biological evaluation of ethacrynic acid derivatives bearing sulfonamides as potent anti-cancer agents (2020, Bioorganic & Medicinal Chemistry Letters)
  • Synthesis and evaluation of a novel class of ethacrynic acid derivatives containing triazoles as potent anticancer agents (2021, Bioorganic Chemistry)

Gérald Guillaumet has frequently collaborated with co-authors including Saïd El Kazzouli, Franck Suzenet, Nabil El Brahmi, Abdelmoula El Abbouchi, and Mohamed Akssira, indicating a collaborative research environment.

The scientist has published in several reputable venues emphasizing chemistry and synthesis research. Frequent publication venues include:

  • Molecules
  • Advanced Synthesis & Catalysis
  • RSC Advances
  • European Journal of Organic Chemistry
  • The Cambridge Structural Database

The cumulative body of work by Gérald Guillaumet demonstrates a consistent focus on chemical synthesis, catalytic processes, and evaluation of bioactive compounds, with significant engagement in the development of heterocyclic compounds and applications related to anticancer activities.

Best Publications

  • New selective ligands of human cloned melatonin MT1 and MT2 receptors.

    Valérie Audinot;François Mailliet;Chantal Lahaye-Brasseur;Anne Bonnaud

  • 3-Aryl-2-quinolone derivatives: synthesis and characterization of in vitro and in vivo antitumor effects with emphasis on a new therapeutical target connected with cell migration.

    Benoît Joseph;Francis Darro;Aurélie Béhard;Brigitte Lesur

  • Functionalization of Imidazo[1,2‐a]pyridines by Means of Metal‐Catalyzed Cross‐Coupling Reactions

    Jamal Koubachi;Saïd El Kazzouli;Mosto Bousmina;Gérald Guillaumet

  • An efficient and reusable heterogeneous catalyst Animal Bone Meal for facile synthesis of benzimidazoles, benzoxazoles, and benzothiazoles

    Yassin Riadi;Yassin Riadi;Rachid Mamouni;Rachid Azzalou;Mohammadine El Haddad

  • Characterization of the melatoninergic MT3 binding site on the NRH:quinone oxidoreductase 2 enzyme.

    François Mailliet;Gilles Ferry;Fanny Vella;Sylvie Berger

  • Copper(I)-Promoted Palladium-Catalyzed Cross-Coupling of Unsaturated Tri-n-butylstannane with Heteroaromatic Thioether

    France-Aimée Alphonse;Franck Suzenet;Anne Keromnes;Bruno Lebret

  • Pyridine-based lanthanide complexes: towards bimodal agents operating as near infrared luminescent and MRI reporters.

    Laurent Pellegatti;Laurent Pellegatti;Jian Zhang;Bohuslav Drahos;Sandrine Villette

  • Synthesis and biological evaluation of new 2-(4,5-dihydro-1H-imidazol-2-yl)-3,4-dihydro-2H-1,4-benzoxazine derivatives.

    Frédérique Touzeau;Axelle Arrault;Gérald Guillaumet;Elizabeth Scalbert

  • Synthesis of polysubstituted imidazo[1,2-a]pyridines via microwave-assisted one-pot cyclization/Suzuki coupling/palladium-catalyzed heteroarylation.

    Jamal Koubachi;Saïd El Kazzouli;Sabine Berteina-Raboin, ,†;and Abderrahim Mouaddib

  • Synthesis and biological evaluation of N-(7-indazolyl)benzenesulfonamide derivatives as potent cell cycle inhibitors

    Unknown

  • New substituted 1,4-benzoxazine derivatives with potential intracellular calcium activity

    A.-S. Bourlot;I. Sanchez;G. Dureng;G. Guillaumet

  • Advances in direct C–H arylation of 5,5- 6,5- and 6,6-fused-heterocycles containing heteroatoms (N, O, S)

    Saïd El Kazzouli;Jamal Koubachi;Nabil El Brahmi;Gérald Guillaumet

  • Design, Synthesis, and Biological Activity of Pyridopyrimidine Scaffolds as Novel PI3K/mTOR Dual Inhibitors

    Thibault Saurat;Frédéric Buron;Nuno Rodrigues;Marie-Ludivine de Tauzia

  • Palladium-catalyzed 3-Thiomethyltriazine-boronic Acid Cross Coupling: Easy Access to 3-Substituted-1,2,4-triazines

    France-Aimée Alphonse;Franck Suzenet;Anne Keromnes;Bruno Lebret

  • Aggressive behavior induced by the steroid sulfatase inhibitor COUMATE and by DHEAS in CBA/H mice.

    Laurent B Nicolas;Walter Pinoteau;Sébastien Papot;Sylvain Routier

  • Expeditious synthesis and cytotoxic activity of new cyanoindolo[3,2-c]quinolines and benzimidazo[1,2-c]quinazolines.

    Christelle Lamazzi;Stéphane Léonce;Bruno Pfeiffer;Pierre Renard

  • SYNTHESIS OF NEW MELATONINERGIC LIGANDS INCLUDING AZAINDOLE MOIETY

    Daniel Mazéas;Gérald Guillaumet;Marie-Claude Viaud

  • Palladium-Catalyzed Oxidative Direct C3- and C7-Alkenylations of Indazoles: Application to the Synthesis of Gamendazole.

    Mohammed Naas;Saïd El Kazzouli;El Mokhtar Essassi;Mosto Bousmina

  • Easy Access to 3- or 5-Heteroarylamino-1,2,4-triazines by SNAr, SNH, and Palladium-Catalyzed N-Heteroarylations

    Ethel Garnier;Jérôme Audoux;Eric Pasquinet;Franck Suzenet

  • Synthesis of 4- and 6-Azaindoles via the Fischer Reaction

    Matthieu Jeanty;Jérôme Blu;Franck Suzenet;Gérald Guillaumet

  • N-substituted oxazolo[5,4-b]pyridin-2(1H)-ones: a new class of non-opiate antinociceptive agents.

    Marie-Claude Viaud;Patricia Jamoneau;Christine Flouzat;Jean-Guy Bizot-Espiard

Frequent Co-Authors

Jean-Michel Léger
Jean-Michel Léger University of Poitiers
Thierry Besson
Thierry Besson University of Rouen
Robert Kiss
Robert Kiss Université Libre de Bruxelles
Philippe Delagrange
Philippe Delagrange Centre national de la recherche scientifique, CNRS
Jean A. Boutin
Jean A. Boutin Institut de Recherches Internationales Servier
Laurent Meijer
Laurent Meijer Perha Pharmaceuticals
Stéphane Petoud
Stéphane Petoud Centre national de la recherche scientifique, CNRS
Christiane Guguen-Guillouzo
Christiane Guguen-Guillouzo University of Rennes
Jean-Pierre Vilardaga
Jean-Pierre Vilardaga University of Pittsburgh

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