World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
40
Citations
5496
World Ranking
17913
National Ranking
13

Stojan Stavber 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 Stojan Stavber 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: 234 publications — 44th percentile

44% of scientists in this discipline score the same or lower.

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

Stojan Stavber 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 Stojan Stavber 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: 40 D-Index — 1st percentile

1% of scientists in this discipline score the same or lower.

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

Overview

Stojan Stavber is affiliated with the Jožef Stefan Institute in Slovenia and specializes in the field of Chemistry, with a strong focus on Organic Chemistry and related subfields. Their research encompasses various aspects of chemical synthesis, catalytic reactions, and corrosion behavior.

The scientist's main fields of study include:

  • Chemistry

Within this broad domain, they concentrate on several subfields:

  • Organic Chemistry
  • Inorganic Chemistry
  • Molecular Biology
  • Materials Chemistry
  • Civil and Structural Engineering

Their research topics cover a spectrum of areas relevant to synthesis and catalysis, corrosion science, and molecular interactions:

  • Chemical Synthesis and Reactions
  • Synthesis and Catalytic Reactions
  • Catalytic C-H Functionalization Methods
  • Corrosion Behavior and Inhibition
  • Concrete Corrosion and Durability
  • Asymmetric Hydrogenation and Catalysis
  • Crystallography and Molecular Interactions

Stavber has contributed to several peer-reviewed articles in scientific journals, including:

  • "Simplistic correlations between molecular electronic properties and inhibition efficiencies: Do they really exist?", 2020, Corrosion Science
  • "Editors' Choice-The Effect of Anchor Group and Alkyl Backbone Chain on Performance of Organic Compounds as Corrosion Inhibitors for Aluminum Investigated Using an Integrative Experimental-Modeling Approach", 2020, Journal of The Electrochemical Society
  • "Electrophilic Iodination of Organic Compounds Using Elemental Iodine or Iodides: Recent Advances 2008-2021: Part I", 2022, Compounds
  • "N-Halosuccinimides as Precatalysts for C-, N-, O-, and X-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions", 2020, Catalysts
  • "N-Iodosuccinimide as a Precatalyst for Direct Cross-Coupling of Alcohols with C-Nucleophiles under Solvent-Free Reaction Conditions", 2020, Catalysts

Their publications have appeared in multiple venues, with the most frequent being:

  • Catalysts (5 publications)
  • Corrosion Science
  • Journal of The Electrochemical Society
  • Compounds
  • Tetrahedron Letters

Collaboration is a notable component of Stavber's research, with frequent co-authors including:

  • Njomza Ajvazi
  • Anton Kokalj
  • Ingrid Milošev
  • Bojan Božić
  • Matic Lozinšek

Best Publications

  • Electrophilic Iodination of Organic Compounds Using Elemental Iodine or Iodides

    Stojan Stavber;Marjan Jereb;Marko Zupan

  • Bromination of ketones with H2O2–HBr “on water”

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Marko Zupan;Jernej Iskra

  • Halogenation of ketones with N-halosuccinimides under solvent-free reaction conditions

    Igor Pravst;Marko Zupan;Marko Zupan;Stojan Stavber

  • Environmentally benign electrophilic and radical bromination 'on water': H2O2-HBr system versus N-bromosuccinimide

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Jernej Iskra

  • Simplistic correlations between molecular electronic properties and inhibition efficiencies: Do they really exist?

    Anton Kokalj;Matic Lozinšek;Barbara Kapun;Peyman Taheri

  • Iodine as a catalyst for efficient conversion of ketones to gem-dihydroperoxides by aqueous hydrogen peroxide.

    Katja Zmitek;Marko Zupan;Stojan Stavber;Jernej Iskra

  • The effect of iodine on the peroxidation of carbonyl compounds.

    Katja Zmitek;Marko Zupan;Stojan Stavber;Jernej Iskra

  • Halogenation of organic compounds in ionic liquids

    Jasminka Pavlinac;Marko Zupan;Kenneth K. Laali;Stojan Stavber

  • Selective and effective fluorination of organic compounds in water using Selectfluor F-TEDA-BF4.

    Gaj Stavber;Marko Zupan;Marjan Jereb;Stojan Stavber

  • Visible light induced ‘on water’ benzylic bromination with N-bromosuccinimide

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Jernej Iskra

  • Recent Advances in the Application of SelectfluorTMF-TEDA-BF4 as a Versatile Mediator or Catalyst in Organic Synthesis

    Stojan Stavber

  • Directed regioselectivity of bromination of ketones with NBS: solvent-free conditions versus water

    Igor Pravst;Marko Zupan;Marko Zupan;Stojan Stavber

  • Selective aerobic oxidative dibromination of alkenes with aqueous HBr and sodium nitrite as a catalyst

    Ajda Podgoršek;Marco Eissen;Jens Fleckenstein;Stojan Stavber

  • Free radical bromination by the H2O2–HBr system on water

    Ajda Podgoršek;Stojan Stavber;Marko Zupan;Marko Zupan;Jernej Iskra

  • Fluorination with cesium fluoroxysulfate. Room-temperature fluorination of benzene and naphthalene derivatives

    Stojan Stavber;Marko Zupan

  • Nonmetal-Catalyzed Iodination of Arenes with Iodide and Hydrogen Peroxide

    Jernej Iskra;Stojan Stavber;Marko Zupan

  • Solvent-free bromination of 1,3-diketones and β-keto esters with NBS

    Igor Pravst;Marko Zupan;Marko Zupan;Stojan Stavber

  • High yield direct fluorofunctionalisation of ketones using AccufluorTM-NFTh fluorinating reagent

    Stojan Stavber;Marko Zupan

  • Ritter-type fluorofunctionalisation as a new, effective method for conversion of alkenes to vicinal fluoroamides

    Stojan Stavber;Tjasa Sotler Pecan;Maja Papež;Marko Zupan

  • Micellar-System-Mediated DirectFluorination of Ketones in Water

    Gaj Stavber;Marko Zupan;Stojan Stavber

Frequent Co-Authors

Ingrid Milošev
Ingrid Milošev Jožef Stefan Institute
Anton Kokalj
Anton Kokalj Jožef Stefan Institute
Boris Sket
Boris Sket University of Ljubljana
John A. Gladysz
John A. Gladysz Texas A&M University
Jean'ne M. Shreeve
Jean'ne M. Shreeve University of Idaho
Barbara Malič
Barbara Malič Jožef Stefan Institute
Kaoru Nakamura
Kaoru Nakamura Kobe University
Atta-ur-Rahman
Atta-ur-Rahman University of Karachi
Marija Kosec
Marija Kosec Jožef Stefan Institute
G. K. Surya Prakash
G. K. Surya Prakash University of Southern California

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