World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
54
Citations
11145
World Ranking
12549
National Ranking
710

John A. Murphy 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 John A. Murphy 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: 218 publications — 39th percentile

39% of scientists in this discipline score the same or lower.

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

John A. Murphy 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 John A. Murphy 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: 54 D-Index — 31st percentile

31% of scientists in this discipline score the same or lower.

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

Research.com Recognitions

  • 2016 - Charles Rees Award, Royal Society of Chemistry (UK) "for his highly innovative studies on the preparation
  • 2012 - Bader Award, Royal Society of Chemistry (UK)
  • 2001 - Fellow of the Royal Society of Edinburgh

Overview

John A. Murphy is affiliated with the University of Strathclyde in the United Kingdom and has a significant publication record in the field of chemistry, particularly within organic chemistry. Their body of work encompasses 82 publications in the main field of chemistry, with 80 focused specifically on organic chemistry. Additional subfields include molecular biology, pulmonary and respiratory medicine, astronomy and astrophysics, and materials chemistry.

Their research topics cover a diverse range of areas within organic chemistry, with notable concentrations in:

  • Catalytic C-H Functionalization Methods
  • Radical Photochemical Reactions
  • Oxidative Organic Chemistry Reactions
  • Sulfur-Based Synthesis Techniques
  • Catalytic Cross-Coupling Reactions
  • Synthesis and Catalytic Reactions
  • Cyclopropane Reaction Mechanisms

Murphy's recent published papers include:

  • "Recent advances in visible light-activated radical coupling reactions triggered by (i) ruthenium, (ii) iridium and (iii) organic photoredox agents" (2021), published in Chemical Society Reviews
  • "Nitrogen-Centered Radicals in Functionalization of sp2 Systems: Generation, Reactivity, and Applications in Synthesis" (2022), published in Chemical Reviews
  • "Bridge Functionalisation of Bicyclo[1.1.1]pentane Derivatives" (2021), published in Angewandte Chemie International Edition
  • "Hi-JAK-ing the ubiquitin system: The design and physicochemical optimisation of JAK PROTACs" (2020), published in Bioorganic & Medicinal Chemistry
  • "Computational Study on the Boundary Between the Concerted and Stepwise Mechanism of Bimolecular SNAr Reactions" (2020), published in Journal of the American Chemical Society

Frequent publication venues for Murphy include:

  • Chemistry - A European Journal
  • Organic Letters
  • Chemical Science
  • Molecules
  • Journal of the American Chemical Society

Their frequent co-authors are Kenneth Clark, Darren L. Poole, Laura Evans, Joseph M. Anderson, and Nicholas D. Measom.

John A. Murphy has been recognized with several awards including the Charles Rees Award from the Royal Society of Chemistry (UK) in 2016 for highly innovative studies, the Bader Award from the Royal Society of Chemistry (UK) in 2012, and was named a Fellow of the Royal Society of Edinburgh in 2001.

Best Publications

  • Reactions of oxyl radicals with DNA.

    Anthony P. Breen;John A. Murphy

  • Recent advances in visible light-activated radical coupling reactions triggered by (i) ruthenium, (ii) iridium and (iii) organic photoredox agents.

    Jonathan D. Bell;John A. Murphy

  • Nitrogen-Centered Radicals in Functionalization of sp2 Systems: Generation, Reactivity, and Applications in Synthesis.

    Unknown

  • KOtBu: A Privileged Reagent for Electron Transfer Reactions?

    Joshua P. Barham;Graeme Coulthard;Katie J. Emery;Eswararao Doni

  • Concerted Nucleophilic Aromatic Substitution Reactions.

    Simon Rohrbach;Andrew J. Smith;Jia Hao Pang;Darren L. Poole

  • Azide rearrangements in electron-deficient systems.

    Stuart Lang;John Murphy

  • Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): Efficient formation of products derived from aryl radicals

    Mohan Mahesh;John A Murphy;Franck LeStrat;Hans Peter Wessel

  • Discovery and development of organic super-electron-donors

    John A. Murphy

  • Organic super-electron-donors: initiators in transition metal-free haloarene–arene coupling

    Shengze Zhou;Greg M. Anderson;Bhaskar Mondal;Eswararao Doni

  • Highly Efficient Reduction of Unactivated Aryl and Alkyl Iodides by a Ground‐State Neutral Organic Electron Donor

    John A. Murphy;Tanweer A. Khan;Sheng-ze Zhou;Douglas W. Thomson

  • Reductive Cleavage of Sulfones and Sulfonamides by a Neutral Organic Super-Electron-Donor (S.E.D.) Reagent

    Fransziska Schoenebeck;John A. Murphy;Sheng-ze Zhou;Yoshitaka Uenoyama

  • Homoleptic crown N-heterocyclic carbene complexes.

    Ross McKie;John A. Murphy;Stuart R. Park;Mark D. Spicer

  • Identifying the roles of amino acids, alcohols and 1,2-diamines as mediators in coupling of haloarenes to arenes

    Shengze Zhou;Eswararao Doni;Greg M. Anderson;Ryan G. Kane

  • The Generation of Aryl Anions by Double Electron Transfer to Aryl Iodides from a Neutral Ground-State Organic Super-Electron Donor

    John A. Murphy;Sheng-ze Zhou;Douglas W. Thomson;Franziska Schoenebeck

  • Applications of organocatalysed visible-light photoredox reactions for medicinal chemistry.

    Michael K. Bogdos;Emmanuel Pinard;John A. Murphy

  • Evolution of neutral organic super-electron-donors and their applications

    Eswararao Doni;John A. Murphy

  • Super-Electron Donors: Bis-pyridinylidene Formation by Base Treatment of Pyridinium Salts

    John A Murphy;Jean Garnier;Stuart R Park;Franziska Schoenebeck

  • A powerful palladium-catalyzed multicomponent process for the preparation of oxazolines and benzoxazoles.

    Patrick J. Boissarie;Zoë E. Hamilton;Stuart Lang;John A. Murphy

  • Electron Transfer to Benzenes by Photoactivated Neutral Organic Electron Donor Molecules

    Elise Cahard;Franziska Schoenebeck;Jean Garnier;Sylvain P. Y. Cutulic

  • Bridge Functionalisation of Bicyclo[1.1.1]pentane Derivatives.

    Joseph M. Anderson;Nicholas D. Measom;John A. Murphy;Darren Lee Poole

  • Concise synthesis of (±)-horsfiline and (±)-coerulescine by tandem cyclisation of iodoaryl alkenyl azides

    Dimitrios E. Lizos;John A. Murphy

  • Metal-free reductive cleavage of C-N and S-N bonds by photoactivated electron transfer from a neutral organic donor

    Steven O'Sullivan;Eswararao Doni;Tell Tuttle;John A Murphy

Frequent Co-Authors

Tell Tuttle
Tell Tuttle University of Strathclyde
Alan R. Kennedy
Alan R. Kennedy University of Strathclyde
Franziska Schoenebeck
Franziska Schoenebeck RWTH Aachen University
Jack E. Baldwin
Jack E. Baldwin University of Oxford
Robert M. Adlington
Robert M. Adlington University of Oxford
James Staunton
James Staunton University of Cambridge
John Parkinson
John Parkinson University of Toronto
Andrew Turner
Andrew Turner Plymouth University
Shunsuke Chiba
Shunsuke Chiba Nanyang Technological University
David C. Sherrington
David C. Sherrington University of Strathclyde

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