World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
56
Citations
12105
World Ranking
11552
National Ranking
3119

Joseph M. Fox 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 Joseph M. Fox 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: 134 publications — 9th percentile

9% of scientists in this discipline score the same or lower.

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

Joseph M. Fox 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 Joseph M. Fox 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: 56 D-Index — 36th percentile

36% of scientists in this discipline score the same or lower.

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

Overview

Joseph M. Fox is affiliated with the University of Delaware in the United States. Their research spans multiple areas within chemistry and related fields, with a focus on organic chemistry and molecular biology. Their work intersects various disciplines including biochemistry, genetics, molecular biology, and medicine.

Fox's primary fields of study include:

  • Chemistry
  • Biochemistry, Genetics and Molecular Biology
  • Medicine

The subfields Fox has contributed to are:

  • Organic Chemistry
  • Molecular Biology
  • Radiology, Nuclear Medicine and Imaging
  • Biomedical Engineering
  • Atomic and Molecular Physics, and Optics

The main topics of their research work involve:

  • Click Chemistry and Applications
  • Chemical Synthesis and Analysis
  • Monoclonal and Polyclonal Antibodies Research
  • Advanced biosensing and bioanalysis techniques
  • Synthesis and Catalytic Reactions
  • Molecular Junctions and Nanostructures
  • Radiopharmaceutical Chemistry and Applications

Their recent papers include:

  • Bioorthogonal chemistry, 2021, published in Nature Reviews Methods Primers
  • Enabling In Vivo Photocatalytic Activation of Rapid Bioorthogonal Chemistry by Repurposing Silicon-Rhodamine Fluorophores as Cytocompatible Far-Red Photocatalysts, 2021, Journal of the American Chemical Society
  • Catalytic Activation of Bioorthogonal Chemistry with Light (CABL) Enables Rapid, Spatiotemporally Controlled Labeling and No-Wash, Subcellular 3D-Patterning in Live Cells Using Long Wavelength Light, 2022, Journal of the American Chemical Society
  • Divergent Synthesis of Monosubstituted and Unsymmetrical 3,6-Disubstituted Tetrazines from Carboxylic Ester Precursors, 2020, Angewandte Chemie International Edition
  • Ligand-Directed Photocatalysts and Far-Red Light Enable Catalytic Bioorthogonal Uncaging inside Live Cells, 2023, Journal of the American Chemical Society

Frequent co-authors who have collaborated with Fox include:

  • Xinqiao Jia
  • He Zhang
  • Christopher W. am Ende
  • Hanyuan Gao
  • Zibo Li

Fox's research has been published predominantly in the following venues:

  • Journal of the American Chemical Society
  • Angewandte Chemie International Edition
  • Angewandte Chemie
  • bioRxiv (Cold Spring Harbor Laboratory)
  • ACS Applied Materials & Interfaces

Best Publications

  • Tetrazine ligation: fast bioconjugation based on inverse-electron-demand Diels-Alder reactivity.

    Melissa L. Blackman;Maksim Royzen;Joseph M. Fox

  • Genetic Encoding of bicyclononynes and trans-cyclooctenes for site-specific protein labeling in vitro and in live mammalian cells via rapid fluorogenic Diels-Alder reactions.

    Kathrin Lang;Lloyd Davis;Stephen Wallace;Mohan Mahesh

  • Highly Active and Selective Catalysts for the Formation of α-Aryl Ketones

    Joseph M. Fox;Xiaohua Huang;and André Chieffi;Stephen L. Buchwald

  • Bioorthogonal chemistry

    Unknown

  • Design and synthesis of highly reactive dienophiles for the tetrazine-trans-cyclooctene ligation.

    Michael T. Taylor;Melissa L. Blackman;Olga Dmitrenko;Joseph M. Fox

  • Genetically encoded tetrazine amino acid directs rapid site-specific in vivo bioorthogonal ligation with trans-cyclooctenes.

    Jason L. Seitchik;Jennifer C. Peeler;Michael T. Taylor;Melissa L. Blackman

  • Diels-Alder cycloaddition for fluorophore targeting to specific proteins inside living cells.

    Daniel S. Liu;Anupong Tangpeerachaikul;Ramajeyam Selvaraj;Michael T. Taylor

  • Conformationally strained trans-cyclooctene with improved stability and excellent reactivity in tetrazine ligation

    Ampofo Darko;Stephen Wallace;Olga Dmitrenko;Melodie M. Machovina

  • trans-Cyclooctene — a stable, voracious dienophile for bioorthogonal labeling

    Ramajeyam Selvaraj;Joseph M Fox

  • Synthesis, Self-Assembly, and Nonlinear Optical Properties of Conjugated Helical Metal Phthalocyanine Derivatives

    Joseph M. Fox;Thomas J. Katz;Sven Van Elshocht;Thierry Verbiest

  • A photochemical synthesis of functionalized trans-cyclooctenes driven by metal complexation.

    Maksim Royzen;Glenn P A Yap;Joseph M Fox

  • Catalytic asymmetric vinylation of ketone enolates.

    André Chieffi;Ken Kamikawa;Jens Åhman;Joseph M. Fox

  • Tetrazine-trans-cyclooctene ligation for the rapid construction of 18F labeled probes

    Zibo Li;Hancheng Cai;Matthew Hassink;Melissa L. Blackman

  • Systematic Evaluation of Bioorthogonal Reactions in Live Cells with Clickable HaloTag Ligands: Implications for Intracellular Imaging.

    Heather E. Murrey;Joshua C. Judkins;Christopher W. am Ende;T. Eric Ballard

  • Chiral Crown Conformation of Rh2(S-PTTL)4: Enantioselective Cyclopropanation with α-Alkyl-α-diazoesters

    Andrew DeAngelis;Olga Dmitrenko;Glenn P. A. Yap;Joseph M. Fox

  • Rhodium(II)-catalyzed enantioselective C-H functionalization of indoles.

    Andrew DeAngelis;Valerie W. Shurtleff;Olga Dmitrenko;Joseph M. Fox

  • Rapid Bioorthogonal Chemistry Turn-on through Enzymatic or Long Wavelength Photocatalytic Activation of Tetrazine Ligation

    Han Zhang;William S. Trout;Shuang Liu;Gabriel A. Andrade

  • Rh-Catalyzed Intermolecular Reactions of Alkynes with α-Diazoesters That Possess β-Hydrogens: Ligand-Based Control over Divergent Pathways

    Patricia Panne;Joseph M. Fox

  • Rh-Catalyzed Intermolecular Reactions of α-Alkyl-α-Diazo Carbonyl Compounds with Selectivity over β-Hydride Migration

    Andrew DeAngelis;Robert Panish;Joseph M. Fox

  • The Use of Catalytic Amounts of CuCl and Other Improvements in the Benzyne Route to Biphenyl‐Based Phosphine Ligands

    Steven Kaye;Joseph M. Fox;Joseph M. Fox;Frederick A. Hicks;Stephen L. Buchwald

  • Rhodium(II)-Catalyzed Enantioselective C-H Functionalizationof Indoles

    A. DeAngelis;V. W. Shurtleff;O. Dmitrenko;J. M. Fox

Frequent Co-Authors

Glenn P. A. Yap
Glenn P. A. Yap University of Delaware
Xinqiao Jia
Xinqiao Jia University of Delaware
Xiaoyuan Chen
Xiaoyuan Chen National University of Singapore
Thomas J. Katz
Thomas J. Katz Columbia University
Jason W. Chin
Jason W. Chin MRC Laboratory of Molecular Biology
Robert D. Bach
Robert D. Bach University of Delaware
David L. Burris
David L. Burris University of Delaware
Richard C. D. Brown
Richard C. D. Brown University of Southampton
Colin Thorpe
Colin Thorpe University of Delaware

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