World's Best Scientists 2026 revealed!
Yong-Qiang Tu

Yong-Qiang Tu

D-Index & Metrics

Chemistry

D-Index
60
Citations
11969
World Ranking
9759
National Ranking
1635

Yong-Qiang Tu 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 Yong-Qiang Tu 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: 256 publications — 51st percentile

51% of scientists in this discipline score the same or lower.

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

Yong-Qiang Tu 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 Yong-Qiang Tu 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: 60 D-Index — 47th percentile

47% of scientists in this discipline score the same or lower.

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

Overview

Yong-Qiang Tu is affiliated with Lanzhou University in China and has contributed extensively to the fields of Chemistry and Materials Science. Their work spans a wide array of subfields including Organic Chemistry, Materials Chemistry, Molecular Biology, Pharmacology, and Inorganic Chemistry.

The research topics covered by Yong-Qiang Tu showcase a significant focus on crystallization and solubility studies, as well as X-ray diffraction techniques in crystallography. Other prominent areas include asymmetric synthesis and catalysis, synthetic organic chemistry methods, catalytic C-H functionalization methods, asymmetric hydrogenation and catalysis, and the synthesis and pharmacology of alkaloids.

Yong-Qiang Tu has published frequently in high-impact scientific venues. Regular publication venues include:

  • The Cambridge Structural Database
  • Angewandte Chemie International Edition
  • Angewandte Chemie
  • Organic Letters
  • Journal of the American Chemical Society

Their recent significant papers include:

  • Recent development and applications of semipinacol rearrangement reactions (2021, Chemical Science)
  • Enantioselective Synthesis of 3,3'-Disubstituted 2-Amino-2'-hydroxy-1,1'-binaphthyls by Copper-Catalyzed Aerobic Oxidative Cross-Coupling (2020, Angewandte Chemie International Edition)
  • Atroposelective Synthesis of Axially Chiral 3-Arylindoles by Copper-Catalyzed Asymmetric Cross-Coupling of Indoles with Quinones and Naphthoquinones (2020, Organic Letters)
  • Enantioselective Construction of 2-Aryl-2,3-dihydrobenzofuran Scaffolds Using Cu/SPDO-Catalyzed [3 + 2] Cycloaddition (2021, Organic Letters)
  • An efficient approach to angular tricyclic molecular architecture via Nazarov-like cyclization and double ring-expansion cascade (2022, Nature Communications)

Collaboration is a notable aspect of their research, with frequent co-authors including Xiao-Ming Zhang, Fu-Min Zhang, Ka Lu, and Si-Hua Hou, reflecting active teamwork in advancing their scientific investigations.

Best Publications

  • Direct Sp3α-C-H activation and functionalization of alcohol and ether.

    Shu-Yu Zhang;Fu-Min Zhang;Yong-Qiang Tu

  • Semipinacol rearrangement in natural product synthesis.

    Zhen-Lei Song;Zhen-Lei Song;Chun-An Fan;Yong-Qiang Tu

  • Stereoselective Construction of Quaternary Carbon Stereocenters via a Semipinacol Rearrangement Strategy

    Baomin Wang;Yong Qiang Tu

  • Radical aryl migration reactions and synthetic applications.

    Zhi-Min Chen;Xiao-Ming Zhang;Yong-Qiang Tu;Yong-Qiang Tu

  • Microwave-promoted three-component coupling of aldehyde, alkyne, and amine via C-H activation catalyzed by copper in water.

    Lei Shi;Yong-Qiang Tu;Min Wang;Fu-Min Zhang

  • Copper-catalyzed tandem trifluoromethylation/semipinacol rearrangement of allylic alcohols.

    Zhi-Min Chen;Wei Bai;Shao-Hua Wang;Bin-Miao Yang

  • Highly efficient and recyclable heterogeneous asymmetric transfer hydrogenation of ketones in water.

    Pei Nian Liu;Jin Gen Deng;Yong Qiang Tu;Shao Hua Wang

  • Efficient heterogeneous asymmetric transfer hydrogenation of ketones using highly recyclable and accessible silica-immobilized Ru-TsDPEN catalysts.

    Pei Nian Liu;Pei Ming Gu;Fei Wang;Yong Qiang Tu

  • Organocatalytic Asymmetric Vinylogous α-Ketol Rearrangement: Enantioselective Construction of Chiral All-Carbon Quaternary Stereocenters in Spirocyclic Diketones via Semipinacol-Type 1,2-Carbon Migration

    En Zhang;Chun-An Fan;Yong-Qiang Tu;Fu-Min Zhang

  • Organocatalytic asymmetric halogenation/semipinacol rearrangement: highly efficient synthesis of chiral α-oxa-quaternary β-haloketones.

    Zhi-Min Chen;Qing-Wei Zhang;Zhi-Hua Chen;Hui Li

  • A reaction for sp(3)-sp(3) C-C bond formation via cooperation of Lewis acid-promoted/Rh-catalyzed C-H bond activation.

    Lei Shi;Yong-Qiang Tu;Min Wang;Fu-Min Zhang

  • Iron(III)‐Catalyzed and Air‐Mediated Tandem Reaction of Aldehydes, Alkynes and Amines: An Efficient Approach to Substituted Quinolines

    Ke Cao;Fu-Min Zhang;Yong-Qiang Tu;Xiao-Tao Zhuo

  • Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis

    Xiao-Ming Zhang;Yong-Qiang Tu;Yong-Qiang Tu;Fu-Min Zhang;Zhi-Hua Chen

  • Brønsted Acid catalyzed enantioselective semipinacol rearrangement for the synthesis of chiral spiroethers.

    Qing-Wei Zhang;Chun-An Fan;Hai-Jun Zhang;Yong-Qiang Tu

  • Iron‐Catalyzed C(sp3)C(sp3) Bond Formation through C(sp3)H Functionalization: A Cross‐Coupling Reaction of Alcohols with Alkenes

    Shu-Yu Zhang;Yong-Qiang Tu;Chun-An Fan;Fu-Min Zhang

  • Rapid and efficient microwave-assisted amination of electron-rich aryl halides without a transition-metal catalyst.

    Lei Shi;Min Wang;Chun-An Fan;Fu-Min Zhang

  • Organocatalytic Asymmetric Direct C sp 3H Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers

    Zhi-Wei Jiao;Shu-Yu Zhang;Chuan He;Yong-Qiang Tu

  • Catalytic asymmetric semipinacol rearrangements

    Shao-Hua Wang;Bao-Sheng Li;Yong-Qiang Tu

  • Enantioselective bromination/semipinacol rearrangement for the synthesis of β-bromoketones containing an all-α-carbon quaternary center

    Hui Li;Fu-Min Zhang;Yong-Qiang Tu;Qing-Wei Zhang

  • Copper-Complex-Catalyzed Asymmetric Aerobic Oxidative Cross-Coupling of 2-Naphthols: Enantioselective Synthesis of 3,3'-Substituted C1 -Symmetric BINOLs.

    Jin-Miao Tian;Ai-Fang Wang;Ju-Song Yang;Xiao-Jing Zhao

  • Efficient Heterogeneous Asymmetric Transfer Hydrogenation Catalyzed by Recyclable Silica‐Supported Ruthenium Complexes

    Pei-Nian Liu;Pei-Ming Gu;Jin-Gen Deng;Yong-Qiang Tu

Frequent Co-Authors

Shu-Yu Zhang
Shu-Yu Zhang Shanghai Jiao Tong University
Jingen Deng
Jingen Deng Sichuan University
Zhi-Xiang Yu
Zhi-Xiang Yu Peking University
Albert S. C. Chan
Albert S. C. Chan Sun Yat-sen University
Qi-Lin Zhou
Qi-Lin Zhou Nankai University
Yong Lu
Yong Lu East China Normal University
Jian-Hua Xie
Jian-Hua Xie Nankai University
Chuan He
Chuan He University of Chicago
Yong-Tang Zheng
Yong-Tang Zheng Kunming Institute of Zoology
Jiantao Zai
Jiantao Zai Shanghai Jiao Tong University

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