World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
57
Citations
12241
World Ranking
11035
National Ranking
1779

Guo-Qiang Lin 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 Guo-Qiang Lin 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: 421 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.

Guo-Qiang Lin 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 Guo-Qiang Lin 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: 57 D-Index — 39th percentile

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

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

Overview

Guo-Qiang Lin is a researcher affiliated with the Chinese Academy of Sciences in China, with a significant body of work spanning chemistry, medicine, and biochemistry, genetics, and molecular biology. Their research output includes 187 publications in chemistry, 116 in medicine, and 87 in biochemistry and related fields. Within these areas, they have contributed extensively to organic chemistry, molecular biology, pharmacology, inorganic chemistry, and pulmonary and respiratory medicine.

Their scientific inquiries focus on several key topics including catalytic C-H functionalization methods, asymmetric hydrogenation and catalysis, synthetic organic chemistry methods, catalytic cross-coupling reactions, asymmetric synthesis and catalysis, cyclopropane reaction mechanisms, and catalytic alkyne reactions.

Guo-Qiang Lin has authored multiple papers in well-regarded scientific journals. Notable publications include:

  • Stereodivergent Synthesis of Tertiary Fluoride-Tethered Allenes via Copper and Palladium Dual Catalysis, 2021, Journal of the American Chemical Society
  • Glycyrrhizic acid exerts inhibitory activity against the spike protein of SARS-CoV-2, 2020, Phytomedicine
  • Bacteria-Anchoring Hybrid Liposome Capable of Absorbing Multiple Toxins for Antivirulence Therapy of Escherichia coli Infection, 2021, ACS Nano
  • Catalytic Asymmetric Hydroalkoxylation and Formal Hydration and Hydroaminoxylation of Conjugated Dienes, 2023, Journal of the American Chemical Society
  • Copper(I)-catalyzed diastereo- and enantio-selective construction of optically pure exocyclic allenes, 2020, Nature Communications

Their frequent publication venues also include Organic Letters, Chemical Communications, PubMed, Advanced Synthesis & Catalysis, and Blood, reflecting diverse interests and interdisciplinary collaboration.

Guo-Qiang Lin has collaborated regularly with several researchers, including Ping Tian, Chen-Guo Feng, Dingding Gao, Zhi-Tao He, and Mengyao Li. These frequent co-authorships indicate active research partnerships contributing to the breadth and depth of their scientific investigations.

The scholar's work emphasizes catalytic methods and asymmetric catalysis, integrating synthetic organic chemistry approaches with biological and pharmacological applications. This multidisciplinary engagement is documented by publications in both chemistry-focused and biomedical journals, illustrating a crossover of chemical synthesis and medical research.

Best Publications

  • Rhodium-Catalyzed Asymmetric Arylation

    Ping Tian;Han-Qing Dong;Guo-Qiang Lin

  • Design of C2-symmetric tetrahydropentalenes as new chiral diene ligands for highly enantioselective Rh-catalyzed arylation of N-tosylarylimines with arylboronic acids.

    Zhi-Qian Wang;Chen-Guo Feng;Ming-Hua Xu;Guo-Qiang Lin

  • An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines.

    Guo-Qiang Lin;Ming-Hua Xu;Yu-Wu Zhong;Xing-Wen Sun

  • Cu-Catalyzed Asymmetric Borylative Cyclization of Cyclohexadienone-Containing 1,6-Enynes

    Ping Liu;Yuki Fukui;Ping Tian;Ping Tian;Zhi-Tao He;Zhi-Tao He

  • Cu-catalyzed asymmetric borylative cyclization of cyclohexadienone-containing 1,6-enynes.

    Ping Liu;Yuki Fukui;Ping Tian;Zhi-Tao He

  • Tunable Arylative Cyclization of 1,6-Enynes Triggered by Rhodium(III)-Catalyzed C–H Activation

    Yuki Fukui;Ping Liu;Qiang Liu;Zhi-Tao He

  • Chiral Drugs: Chemistry and Biological Action

    Guo-Qiang Lin;Qi-Dong You;Jie-Fei Cheng

  • Principles and applications of asymmetric synthesis

    Guo-Qiang Lin;Yue-Ming Li;Albert Sun-Chi Chan

  • Stereodivergent Synthesis of Tertiary Fluoride-Tethered Allenes via Copper and Palladium Dual Catalysis

    Unknown

  • Remarkable salt effect on In-mediated allylation of N-tert-butanesulfinyl imines in aqueous media: highly practical asymmetric synthesis of chiral homoallylic amines and isoindolinones.

    Xing-Wen Sun;Min Liu;Ming-Hua Xu;Guo-Qiang Lin

  • Borylation of Olefin C-H Bond via Aryl to Vinyl Palladium 1,4-Migration.

    Tian-Jiao Hu;Ge Zhang;Ya-Heng Chen;Chen-Guo Feng

  • Rhodium-catalyzed asymmetric conjugate addition of organoboronic acids to nitroalkenes using chiral bicyclo[3.3.0] diene ligands.

    Zhi-Qian Wang;Chen-Guo Feng;Shu-Sheng Zhang;Ming-Hua Xu

  • Room-temperature highly diastereoselective Zn-mediated allylation of chiral N-tert-butanesulfinyl imines: remarkable reaction condition controlled stereoselectivity reversal.

    Xing-Wen Sun;Ming-Hua Xu;Guo-Qiang Lin

  • Chiral Diene as the Ligand for the Synthesis of Axially Chiral Compounds via Palladium-Catalyzed Suzuki−Miyaura Coupling Reaction

    Shu-Sheng Zhang;Zhi-Qian Wang;Ming-Hua Xu;Guo-Qiang Lin

  • A highly efficient and direct approach for synthesis of enantiopure beta-amino alcohols by reductive cross-coupling of chiral N-tert-butanesulfinyl imines with aldehydes.

    Yu-Wu Zhong;Yi-Zhou Dong;Kai Fang;Kenji Izumi

  • Asymmetric Synthesis of β-Substituted γ-Lactams via Rhodium/Diene-Catalyzed 1,4-Additions: Application to the Synthesis of (R)-Baclofen and (R)-Rolipram

    Cheng Shao;Hong-Jie Yu;Nuo-Yi Wu;Ping Tian

  • Glycyrrhizic acid exerts inhibitory activity against the spike protein of SARS-CoV-2

    Unknown

  • Highly Enantioselective Arylation of N-Tosylalkylaldimines Catalyzed by Rhodium-Diene Complexes

    Zhe Cui;Hong-Jie Yu;Rui-Feng Yang;Wen-Yun Gao

  • Catalytic Enantioselective Synthesis of Chiral Phthalides by Efficient Reductive Cyclization of 2-Acylarylcarboxylates under Aqueous Transfer Hydrogenation Conditions

    Bo Zhang;Ming-Hua Xu;Guo-Qiang Lin

  • Efficient Access to Bicyclo[4.3.0]nonanes: Copper‐Catalyzed Asymmetric Silylative Cyclization of Cyclohexadienone‐Tethered Allenes

    Zhi‐Tao He;Xiao‐Qi Tang;Li‐Bo Xie;Mian Cheng

  • Highly practical catalytic asymmetric 1,4-addition of arylboronic acids in water using new hydrophilic chiral bicyclo[3.3.0] diene ligands

    Chen-Guo Feng;Zhi-Qian Wang;Cheng Shao;Ming-Hua Xu

  • Identification, purification and characterization of β-glucosidase from apple seed as a novel catalyst for synthesis of O-glucosides

    Hui-Lei Yu;Jian-He Xu;Wen-Ya Lu;Guo-Qiang Lin

  • Rhodium‐Catalyzed Asymmetric Arylative Cyclization of meso‐1,6‐Dienynes Leading to Enantioenriched cis‐Hydrobenzofurans

    Zhi-Tao He;Bing Tian;Bing Tian;Yuki Fukui;Xiaofeng Tong

  • Asymmetric reduction of ketones by employing Rhodotorula sp. AS2.2241 and synthesis of the β-blocker (R)-nifenalol

    Wei Yang;Jian-He Xu;Yan Xie;Yi Xu

  • Samarium diiodide-induced asymmetric synthesis of optically pure unsymmetrical vicinal diamines by reductive cross-coupling of nitrones with N-tert-butanesulfinyl imines.

    Yu-Wu Zhong;Ming-Hua Xu;Guo-Qiang Lin

Frequent Co-Authors

Ming-Hua Xu
Ming-Hua Xu Southern University of Science and Technology
Min Liu
Min Liu Central South University
Yu-Wu Zhong
Yu-Wu Zhong Chinese Academy of Sciences
Qiang Liu
Qiang Liu Chinese Academy of Sciences
Qidong You
Qidong You China Pharmaceutical University

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