World's Best Scientists 2026 revealed!
Richard Goddard

Richard Goddard

D-Index & Metrics

Chemistry

D-Index
75
Citations
22098
World Ranking
4407
National Ranking
325

Richard Goddard 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 Richard Goddard 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: 506 publications — 89th percentile

89% of scientists in this discipline score the same or lower.

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

Richard Goddard 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 Richard Goddard 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: 75 D-Index — 76th percentile

76% of scientists in this discipline score the same or lower.

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

Overview

Richard Goddard is affiliated with the Max Planck Society in Germany and conducts research primarily in materials science and chemistry. Their scholarly work spans multiple subfields, including materials chemistry, organic chemistry, molecular biology, inorganic chemistry, and physical and theoretical chemistry.

The main topics of Goddard's research encompass crystallization and solubility studies, X-ray diffraction in crystallography, quinazolinone synthesis and applications, phenothiazines and benzothiazines synthesis and activities, synthesis and biological activity, crystallography and molecular interactions, and cancer therapeutics and mechanisms.

The scientist has published extensively in several key venues, reflecting a focus on crystallographic and chemical research. Frequent publication venues include:

  • The Cambridge Structural Database
  • Acta Crystallographica Section E Crystallographic Communications
  • Journal of Chemical Crystallography
  • Molbank
  • Journal of the American Chemical Society

Richard Goddard's recent papers span from 2020 to 2025 and cover a wide range of chemical and materials science topics. Notable publications include:

  • "Synthesis and isolation of a triplet bismuthinidene with a quenched magnetic response" (2023, Science)
  • "A New Ligand Design Based on London Dispersion Empowers Chiral Bismuth-Rhodium Paddlewheel Catalysts" (2021, Journal of the American Chemical Society)
  • "Hydrogenative Metathesis of Enynes via Piano-Stool Ruthenium Carbene Complexes Formed by Alkyne gem-Hydrogenation" (2020, Journal of the American Chemical Society)
  • "Synthesis and Characterization of Phenylalanine Amides Active against Mycobacterium abscessus and Other Mycobacteria" (2023, Journal of Medicinal Chemistry)
  • "Spiro-C(sp 3)-atom transfer: Creating rigid three-dimensional structures with Ph2 SCN2" (2025, Science)

Frequent collaborators in Goddard's research include:

  • Rüdiger W. Seidel
  • Adrian Richter
  • Peter Imming
  • Nils Nöthling
  • Christoph Lehmann

Best Publications

  • Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands.

    Alois Fürstner;Lutz Ackermann;Barbara Gabor;Richard Goddard

  • Preparation, Structure, and Reactivity of Nonstabilized Organoiron Compounds. Implications for Iron-Catalyzed Cross Coupling Reactions

    Alois Fürstner;Rubén Martin;Helga Krause;Günter Seidel

  • Novel Coordination of (Benzoylmethylene)triphenylphosphorane in a Nickel Oligomerization Catalyst

    Wilhelm Keim;Frank H. Kowaldt;Richard Goddard;Carl Krüger

  • Coordination Chemistry of Ene‐1,1‐diamines and a Prototype “Carbodicarbene”

    Alois Fürstner;Manuel Alcarazo;Richard Goddard;Christian W. Lehmann

  • An N-heterocyclic carbene ligand with flexible steric bulk allows Suzuki cross-coupling of sterically hindered aryl chlorides at room temperature.

    Gereon Altenhoff;Richard Goddard;Christian W. Lehmann;Frank Glorius

  • A Cheap Metal for a “Noble” Task: Preparative and Mechanistic Aspects of Cycloisomerization and Cycloaddition Reactions Catalyzed by Low-Valent Iron Complexes

    Alois Fürstner;Kaisuke Majima;Rubén Martín;Helga Krause

  • Practical new silyloxy-based alkyne metathesis catalysts with optimized activity and selectivity profiles.

    Johannes Heppekausen;Robert Stade;Richard Goddard;Alois Fürstner

  • Direct catalytic asymmetric synthesis of cyclic aminals from aldehydes.

    Xu Cheng;Sreekumar Vellalath;Richard Goddard;Benjamin List

  • Oxazolines as chiral building blocks for imidazolium salts and N-heterocyclic carbene ligands

    Frank Glorius;Gereon Altenhoff;Richard Goddard;Christian W. Lehmann

  • Multifunctional “Clickates” as Versatile Extended Heteroaromatic Building Blocks: Efficient Synthesis via Click Chemistry, Conformational Preferences, and Metal Coordination

    Robert M. Meudtner;Marc Ostermeier;Richard Goddard;Christian Limberg

  • Enantioselective Gold Catalysis: Opportunities Provided by Monodentate Phosphoramidite Ligands with an Acyclic TADDOL Backbone

    Henrik Teller;Susanne Flügge;Richard Goddard;Alois Fürstner

  • Efficient asymmetric hydrogenation of pyridines.

    Frank Glorius;Nick Spielkamp;Sigrid Holle;Richard Goddard

  • Crystallization of Large Planar Polycyclic Aromatic Hydrocarbons: The Molecular and Crystal Structures of Hexabenzo[bc,ef,hi,kl,no,qr]coronene and Benzo[1,2,3-bc:4,5,6-b'c']dicoronene

    Richard Goddard;Matthias W. Haenel;William C. Herndon;Carl Krueger

  • Total syntheses of the phytotoxic lactones herbarumin I and II and a synthesis-based solution of the pinolidoxin puzzle.

    Alois Fürstner;Karin Radkowski;Conny Wirtz;Richard Goddard

  • First enantioselective catalysis using a helical diphosphane

    Manfred T Reetz;Eckart W Beuttenmüller;Richard Goddard

  • Optimized synthesis, structural investigations, ligand tuning and synthetic evaluation of silyloxy-based alkyne metathesis catalysts.

    Johannes Heppekausen;Robert Stade;Azusa Kondoh;Günter Seidel

  • One-Point Binding Ligands for Asymmetric Gold Catalysis: Phosphoramidites with a TADDOL-Related but Acyclic Backbone

    Henrik Teller;Matthieu Corbet;Luca Mantilli;Gopinadhanpillai Gopakumar

  • Synthesis of TRIP and Analysis of Phosphate Salt Impurities

    Martin Klussmann;Lars Ratjen;Sebastian Hoffmann;Vijay Wakchaure

  • Direct catalytic asymmetric three-component Kabachnik-Fields reaction.

    Xu Cheng;Richard Goddard;Gernot Buth;Benjamin List

  • Synthesis of Versatile Chiral N,P Ligands Derived from Pyridine and Quinoline

    William J. Drury;Nicole Zimmermann;Martine Keenan;Masahiko Hayashi

  • Comparative Investigation of Ruthenium-Based Metathesis Catalysts Bearing N-Heterocyclic Carbene (NHC) Ligands.

    Alois Fuerstner;Lutz Ackermann;Barbara Gabor;Richard Goddard

  • Preparation, Structure, and Reactivity of Nonstabilized Organoiron Compounds. Implications for Iron-Catalyzed Cross-Coupling Reactions.

    Alois Fuerstner;Ruben Martin;Helga Krause;Guenter Seidel

Frequent Co-Authors

Carl Krüger
Carl Krüger Max Planck Society
Manfred T. Reetz
Manfred T. Reetz Max Planck Society
Alois Fürstner
Alois Fürstner Max Planck Society
Christian W. Lehmann
Christian W. Lehmann Max Planck Society
Manuel Alcarazo
Manuel Alcarazo University of Göttingen
Walter Thiel
Walter Thiel Max Planck Society
Richard Mynott
Richard Mynott Max Planck Society
Eckhard Bill
Eckhard Bill Max Planck Society
Günther Wilke
Günther Wilke Max Planck Society
Benjamin List
Benjamin List Max Planck Society

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Related Online Degrees & Career Pathways

Studying Chemistry in the USA opens doors to diverse career opportunities, many of which can be enhanced through specialized online degrees. For those interested in the healthcare sector, becoming a pharmacist is a popular path. However, it’s important to consider how much does it cost to become a pharmacist, as the educational investment can be significant.

Another promising option involves the pharmaceutical industry, where careers like pharmaceutical sales representatives offer dynamic roles. Before pursuing this path, understanding the pharmaceutical rep salary and related career paths can help set realistic expectations.

For those drawn to forensic science, starting as a forensic autopsy technician can be both challenging and rewarding. To explore this field, check detailed insights on becoming a forensic autopsy technician, including the education requirements and job outlook.

Additionally, students interested in cost-effective training options can explore programs like the cheapest online forensic science degree, which provide affordable routes to enter the forensic chemistry field.

Best Scientists Citing Richard Goddard

Trending Scientists

Recently Published Articles