World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
62
Citations
13114
World Ranking
8861
National Ranking
492

Keisuke Suzuki 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 Keisuke Suzuki 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: 413 publications — 82nd percentile

82% of scientists in this discipline score the same or lower.

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

Keisuke Suzuki 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 Keisuke Suzuki 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: 62 D-Index — 52nd percentile

52% of scientists in this discipline score the same or lower.

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

Overview

Keisuke Suzuki is affiliated with the University of Sussex in the United Kingdom and specializes in the field of Chemistry, with a strong focus on Organic Chemistry. The breadth of their research includes Toxicology, Pharmacology, Molecular Biology, and Materials Chemistry, highlighting a multidisciplinary approach to chemical sciences.

The researcher's work addresses several main topics, including:

  • Bioactive Compounds and Antitumor Agents
  • Chemical synthesis and alkaloids
  • Synthesis of Indole Derivatives
  • Oxidative Organic Chemistry Reactions
  • Synthetic Organic Chemistry Methods
  • Synthesis and Catalytic Reactions
  • Traditional and Medicinal Uses of Annonaceae

Keisuke Suzuki has contributed extensively to scientific literature, with notable recent papers such as:

  • "Intramolecular Benzyne-Phenolate [4+2] Cycloadditions" (2020, Angewandte Chemie International Edition)
  • "Enantioselective Total Syntheses of Preussomerins: Control of Spiroacetal Stereogenicity by Photochemical Reaction of a Naphthoquinone through 1,6-Hydrogen Atom Transfer" (2022, Angewandte Chemie International Edition)
  • "Evaluation of Amyloid Polypeptide Aggregation Inhibition and Disaggregation Activity of A-Type Procyanidins" (2021, Pharmaceuticals)
  • "Model Study toward Total Synthesis of Dimeric Pyranonaphthoquinones: Synthesis of Hemi-Actinorhodin" (2021, Bulletin of the Chemical Society of Japan)
  • "Understanding the reaction behavior of alanine under hydrothermal conditions through a network model" (2023, Chemical Engineering Journal)

Frequent co-authors in Suzuki's collaborations include:

  • Ken Ohmori
  • Yoshio Ando
  • Daichi Ogawa
  • Vipul V. Betkekar
  • Takumi Fukazawa

Keisuke Suzuki's work is regularly published in a range of scientific journals. Frequent publication venues comprise:

  • Synlett
  • Angewandte Chemie International Edition
  • Angewandte Chemie
  • Organic Letters
  • The Cambridge Structural Database

Their research spans various methods and applications within synthetic and oxidative organic chemistry, extending to medicinal chemistry and studies of bioactive natural products. This range reflects a focus on synthesis, catalytic reactions, and exploration of chemical compounds with biological activity, contributing to knowledge in multiple intersecting domains of chemistry.

Best Publications

  • Finite, Spherical Coordination Networks that Self‐Organize from 36 Small Components

    Masahide Tominaga;Keisuke Suzuki;Masaki Kawano;Takahiro Kusukawa

  • Total Synthesis of Aryl C-Glycoside Natural Products: Strategies and Tactics

    Kei Kitamura;Yoshio Ando;Takashi Matsumoto;Keisuke Suzuki

  • Enantioface-differentiating (asymmetric) addition of alkyllithium and dialkylmagnesium to aldehydes by using (2S,2'S)-2-hydroxymethyl-1-[(1-alkylpyrrolidin-2-yl)methyl]pyrrolidines as chiral ligands

    Teruaki Mukaiyama;Kenso Soai;Toshio Sato;Hisashi Shimizu

  • Total synthesis of the gilvocarcins

    Takamitsu Hosoya;Eiji Takashiro;Takashi Matsumoto;Keisuke Suzuki

  • Catalytic enantioselective crossed aldehyde-ketone benzoin cyclization

    Hiroshi Takikawa;Yoshifumi Hachisu;Jeffrey W. Bode;Jeffrey W. Bode;Keisuke Suzuki

  • New glycosidation reaction 1: Combinational use of Cp2ZrCl2-AgClO4 for activation of glycosyl fluorides and application to highly β-selective gylcosidation of D-mycinose

    Takashi Matsumoto;Hideki Maeta;Keisuke Suzuki;late Gen-ichi Tsuchihashi

  • Aryne-based strategy in the total synthesis of naturally occurring polycyclic compounds.

    Hiroshi Takikawa;Arata Nishii;Takahiro Sakai;Keisuke Suzuki

  • Catalytic intramolecular crossed aldehyde--ketone benzoin reactions: a novel synthesis of functionalized preanthraquinones.

    Yoshifumi Hachisu;Jeffrey W. Bode;Keisuke Suzuki

  • New approach to C-aryl glycosides starting from phenol and glycosyl fluoride. Lewis acid-catalyzed rearrangement of O-glycoside to C-glycoside

    Takashi Matsumoto;Miyoko Katsuki;Keisuke Suzuki

  • An improved procedure for metallocene-promoted glycosidation. Enhanced reactivity by employing 1:2-ratio of Cp2HfCl2-AgClO4

    Keisuke Suzuki;Hideki Maeta;Takashi Matsumoto

  • 4-O-Benzyl-23-O-isopropylidene-L-threose: A useful building block for stereoselective synthesis of monosaccharides

    Teruaki Mukaiyama;Keisuke Suzuki;Tohru Yamada;Fujio Tabusa

  • Total synthesis and absolute stereochemical assignment of gilvocarcin M.

    Takashi Matsumoto;Takamitsu Hosoya;Keisuke Suzuki

  • Modified Chiral Triazolium Salts for Enantioselective Benzoin Cyclization of Enolizable Keto-Aldehydes: Synthesis of (+)-Sappanone B

    Hiroshi Takikawa;Keisuke Suzuki

  • New efficient protocol for aryne generation. Selective synthesis of differentially protected 1,4,5-naphthalenetriols

    Takashi Matsumoto;Takamitsu Hosoya;Miyoko Katsuki;Keisuke Suzuki

  • New glycosidation reaction 2. preparation of 1-fluoro-d-desosamine derivative and its efficient glycosidation by the use of Cp2HfCl2-AgClO4 as the activator

    Keisuke Suzuki;Hideki Maeta;Takashi Matsumoto;late Gen-ichi Tsuchihashi

  • From Axial Chirality to Central Chiralities: Pinacol Cyclization of 2,2'-Biaryldicarbaldehyde to trans-9,10-Dihydrophenanthrene-9,10-diol.

    Ken Ohmori;Mitsuru Kitamura;Keisuke Suzuki

  • Epoxy silyl ether rearrangements: a new, stereoselective approach to the synthesis of .beta.-hydroxy carbonyl compounds

    Keiji. Maruoka;Masaichi. Hasegawa;Hisashi. Yamamoto;Keisuke. Suzuki

  • Convergent total synthesis of vineomycinone B2 methyl ester and its C(12)-epimer

    Takashi Matsumoto;Miyoko Katsuki;Hideki Jona;Keisuke Suzuki

  • On the stereochemistry of aryl C-glycosides: Unusual behavior of bis-TBDPS protected aryl C-olivosides

    Takamitsu Hosoya;Yoriko Ohashi;Takashi Matsumoto;Keisuke Suzuki

  • Cp2ZrCl2AgBF4 in Benzene: A new reagent system for rapid and highly selective α-mannoside synthesis from tetra-O-benzyl-d-mannosyl fluoride

    Keisuke Suzuki;Hideki Maeta;Toshiyuki Suzuki;Takashi Matsumoto

Frequent Co-Authors

Takashi Matsumoto
Takashi Matsumoto Tokyo University of Pharmacy and Life Sciences
Teruaki Mukaiyama
Teruaki Mukaiyama Kitasato University
Hidehiro Uekusa
Hidehiro Uekusa Tokyo Institute of Technology
Tohru Yamada
Tohru Yamada Keio University
Makoto Fujita
Makoto Fujita University of Tokyo
Takeshi Ohkuma
Takeshi Ohkuma Hokkaido University
Kenso Soai
Kenso Soai Tokyo University of Science
Keiji Maruoka
Keiji Maruoka Kyoto University
Masaki Kawano
Masaki Kawano Tokyo Institute of Technology

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