World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
88
Citations
21402
World Ranking
2351
National Ranking
433

Feng Shi 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 Feng Shi 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: 343 publications — 72nd percentile

72% of scientists in this discipline score the same or lower.

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

Feng Shi 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 Feng Shi 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: 88 D-Index — 88th percentile

88% of scientists in this discipline score the same or lower.

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

Overview

Feng Shi is affiliated with Jiangsu Normal University in China and specializes primarily in the field of Chemistry, with a significant focus on Organic Chemistry. The research spans various subfields including Spectroscopy, Pharmacology, Molecular Biology, and Materials Chemistry.

Their research topics explore a range of subjects such as:

  • Axial and Atropisomeric Chirality Synthesis
  • Asymmetric Synthesis and Catalysis
  • Molecular spectroscopy and chirality
  • Synthesis of Indole Derivatives
  • Oxidative Organic Chemistry Reactions
  • Alkaloids: synthesis and pharmacology
  • Catalytic C-H Functionalization Methods

Feng Shi has contributed to several recent papers notable within the scientific community, including:

  • Organocatalytic Atroposelective Synthesis of Indole Derivatives Bearing Axial Chirality: Strategies and Applications, 2022, Accounts of Chemical Research
  • Catalytic Asymmetric Construction of Axially Chiral Indole-Based Frameworks: An Emerging Area, 2020, Chemistry - A European Journal
  • Progresses in organocatalytic asymmetric dearomatization reactions of indole derivatives, 2020, Organic Chemistry Frontiers
  • Atroposelective Access to Oxindole-Based Axially Chiral Styrenes via the Strategy of Catalytic Kinetic Resolution, 2020, Journal of the American Chemical Society
  • Organocatalytic Atroposelective Synthesis of N−N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation, 2022, Angewandte Chemie International Edition

Frequent co-authors collaborating with Feng Shi include:

  • Yu-Chen Zhang
  • Wei Tan
  • Shao-Fei Ni
  • Tian-Zhen Li
  • Shufang Wu

Their research outputs are published in notable venues such as:

  • Angewandte Chemie International Edition
  • The Journal of Organic Chemistry
  • Angewandte Chemie
  • Chinese Journal of Organic Chemistry
  • arXiv (Cornell University)

Best Publications

  • Brønsted-Acid-Catalyzed Asymmetric Multicomponent Reactions for the Facile Synthesis of Highly Enantioenriched Structurally Diverse Nitrogenous Heterocycles

    Jie Yu;Feng Shi;Liu-Zhu Gong

  • Organocatalytic Asymmetric Synthesis of Indole-Based Chiral Heterocycles: Strategies, Reactions, and Outreach.

    Yu-Chen Zhang;Fei Jiang;Feng Shi

  • Catalytic asymmetric synthesis of spirooxindoles: recent developments

    Guang-Jian Mei;Feng Shi

  • Organocatalytic Atroposelective Synthesis of Indole Derivatives Bearing Axial Chirality: Strategies and Applications.

    Unknown

  • C-H activation/borylation/oxidation: a one-pot unified route to meta-substituted phenols bearing ortho-/para-directing groups.

    Robert E. Maleczka;Feng Shi;Daniel Holmes;Milton R. Smith

  • Design and Enantioselective Construction of Axially Chiral Naphthyl‐Indole Skeletons

    Hong-Hao Zhang;Cong-Shuai Wang;Can Li;Guang-Jian Mei

  • Design and Catalytic Asymmetric Construction of Axially Chiral 3,3′-Bisindole Skeletons

    Chun Ma;Fei Jiang;Feng-Tao Sheng;Yinchun Jiao

  • Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles

    Jia-Jia Zhao;Si-Bing Sun;Sai-Huan He;Qiong Wu

  • Catalytic Asymmetric Construction of Axially Chiral Indole-Based Frameworks: An Emerging Area.

    Tian-Zhen Li;Si-Jia Liu;Wei Tan;Feng Shi

  • Progresses in organocatalytic asymmetric dearomatization reactions of indole derivatives

    Feng-Tao Sheng;Jing-Yi Wang;Wei Tan;Yu-Chen Zhang

  • Organocatalytic Asymmetric Arylative Dearomatization of 2,3‐Disubstituted Indoles Enabled by Tandem Reactions

    Yu-Chen Zhang;Jia-Jia Zhao;Fei Jiang;Si-Bing Sun

  • A Catalytic Asymmetric Isatin-Involved Povarov Reaction: Diastereo- and Enantioselective Construction of Spiro[indolin-3,2′-quinoline] Scaffold

    Feng Shi;Gui-Juan Xing;Ren-Yi Zhu;Wei Tan

  • Catalytic Asymmetric (4+3) Cyclizations of In Situ Generated ortho-Quinone Methides with 2-Indolylmethanols.

    Meng Sun;Chun Ma;Si-Jia Zhou;Sai-Fan Lou

  • Benzyne click chemistry: synthesis of benzotriazoles from benzynes and azides.

    Unknown

  • Diastereo- and Enantioselective Construction of 3,3'-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions.

    Wei Dai;Xiao-Li Jiang;Qiong Wu;Feng Shi

  • Synthesis of 2H-indazoles by the [3 + 2] cycloaddition of arynes and sydnones.

    Chunrui Wu;Yuesi Fang;Richard C. Larock;Feng Shi

  • Organocatalytic Atroposelective Synthesis of N-N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation.

    Unknown

  • Catalytic asymmetric chemoselective 1,3-dipolar cycloadditions of an azomethine ylide with isatin-derived imines: diastereo- and enantioselective construction of a spiro[imidazolidine-2,3′-oxindole] framework

    Yue-Ming Wang;Hong-Hao Zhang;Can Li;Tao Fan

  • Indolylmethanols as Reactants in Catalytic Asymmetric Reactions.

    Guang-Jian Mei;Feng Shi

  • Highly diastereo- and enantioselective construction of a spiro[cyclopenta[b]indole-1,3′-oxindole] scaffold via catalytic asymmetric formal [3+2] cycloadditions

    Wei Tan;Xin Li;Yu-Xin Gong;Meng-Di Ge

  • Catalytic Asymmetric Formal [3+3] Cycloaddition of an Azomethine Ylide with 3-Indolylmethanol: Enantioselective Construction of a Six-Membered Piperidine Framework

    Feng Shi;Ren-Yi Zhu;Wei Dai;Cong-Shuai Wang

  • A Strategy for Synthesizing Axially Chiral Naphthyl‐Indoles: Catalytic Asymmetric Addition Reactions of Racemic Substrates

    Fei Jiang;Ke-Wei Chen;Ping Wu;Yu-Chen Zhang

  • Remote C-H activation via through-space palladium and rhodium migrations.

    Feng Shi;Richard C. Larock

Frequent Co-Authors

Shu-Jiang Tu
Shu-Jiang Tu Jiangsu Normal University
Bo Jiang
Bo Jiang Jiangsu Normal University
Xiaohong Zhang
Xiaohong Zhang Soochow University
Guigen Li
Guigen Li Texas Tech University
Can Li
Can Li Dalian Institute of Chemical Physics
Daqing Shi
Daqing Shi Soochow University
Shun-Jun Ji
Shun-Jun Ji Soochow University
Xian-Yong Wei
Xian-Yong Wei China University of Mining and Technology
Benjamin List
Benjamin List Max Planck Society

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