World's Best Scientists 2026 revealed!

Bo Jiang 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 Bo Jiang 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+

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

Bo Jiang 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 Bo Jiang 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+

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

Overview

Bo Jiang is affiliated with Jiangsu Normal University in China and has established a research profile primarily in the field of Chemistry, with a strong focus on Organic Chemistry.

The research topics that Bo Jiang has contributed to include:

  • Catalytic C-H Functionalization Methods
  • Sulfur-Based Synthesis Techniques
  • Catalytic Alkyne Reactions
  • Radical Photochemical Reactions
  • Wheat and Barley Genetics and Pathology
  • Asymmetric Synthesis and Catalysis
  • Cyclopropane Reaction Mechanisms

Bo Jiang has coauthored extensively with several researchers. The most frequent collaborators include:

  • Wen-Juan Hao (92 publications)
  • Shu-Jiang Tu (46 publications)
  • Lianquan Zhang (29 publications)
  • Dengcai Liu (28 publications)
  • Shunzong Ning (25 publications)

Bo Jiang's scholarly work has appeared in a range of publication venues, with significant representation in:

  • Chemical Communications (14 publications)
  • The Journal of Organic Chemistry (13 publications)
  • Organic Letters (12 publications)
  • Chinese Journal of Organic Chemistry (12 publications)
  • Advanced Synthesis & Catalysis (11 publications)

Among recent papers authored or coauthored by Bo Jiang are the following:

  • Recent developments in 1,6-addition reactions of para-quinone methides (p-QMs), 2020, Organic Chemistry Frontiers
  • The Resurgence of Introgression Breeding, as Exemplified in Wheat Improvement, 2020, Frontiers in Plant Science
  • Electrochemical Annulation-Iodosulfonylation of 1,5-Enyne-containing para-Quinone Methides (p-QMs) to Access (E)-Spiroindenes, 2020, Organic Letters
  • A Palladium Complex as an Asymmetric π-Lewis Base Catalyst for Activating 1,3-Dienes, 2021, Journal of the American Chemical Society
  • Electrocatalytic three-component annulation-halosulfonylation of 1,6-enynes toward 1-indanones using sodium halides as both halogen sources and electrolytes, 2020, Green Chemistry

Bo Jiang has contributed to book publications as well, including a 2023 publication titled Seeds that give revisited: Participatory plant breeding and rural revitalization, published by the Centre de Coopération Internationale en Recherche Agronomique pour le Développement.

Best Publications

  • Multicomponent Reactions for the Synthesis of Heterocycles

    Bo Jiang;Trideep Rajale;Walter Wever;Shu-Jiang Tu

  • Recent developments in 1,6-addition reactions of para-quinone methides (p-QMs)

    Jia-Yin Wang;Wen-Juan Hao;Shu-Jiang Tu;Bo Jiang

  • Catalytic Dual 1,1-H-Abstraction/Insertion for Domino Spirocyclizations

    Jiang-Kai Qiu;Jiang-Kai Qiu;Bo Jiang;Yi-Long Zhu;Yi-Long Zhu;Wen-Juan Hao

  • Recent advances in radical transformations of internal alkynes

    Min-Hua Huang;Wen-Juan Hao;Guigen Li;Guigen Li;Shu-Jiang Tu

  • Four-Component Domino Reaction Leading to Multifunctionalized Quinazolines

    Bo Jiang;Shu-Jiang Tu;Parminder Kaur;Walter Wever

  • New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines

    Ning Ma;Bo Jiang;Ge Zhang;Shu-Jiang Tu

  • Catalytic arylsulfonyl radical-triggered 1,5-enyne-bicyclizations and hydrosulfonylation of α,β-conjugates

    Zhen-Zhen Chen;Shuai Liu;Wen-Juan Hao;Ge Xu

  • Merging [2+2] Cycloaddition with Radical 1,4-Addition: Metal-Free Access to Functionalized Cyclobuta[a]naphthalen-4-ols.

    Feng Liu;Jia-Yin Wang;Peng Zhou;Guigen Li;Guigen Li

  • Recent Advances in Radical-Enabled Bicyclization and Annulation/1,n-Bifunctionalization Reactions.

    Min-Hua Huang;Min-Hua Huang;Wen-Juan Hao;Bo Jiang

  • Ligand-Dependent Activity Engineering of Glutathione Peroxidase-Mimicking MIL-47(V) Metal–Organic Framework Nanozyme for Therapy

    Jiangjiexing Wu;Yijun Yu;Yuan Cheng;Chaoqun Cheng

  • A new cascade halosulfonylation of 1,7-enynes toward 3,4-dihydroquinolin-2(1H)-ones via sulfonyl radical-triggered addition/6-exo-dig cyclization

    Yi-Long Zhu;Bo Jiang;Wen-Juan Hao;Ai-Fang Wang

  • Microwave-Assisted Multicomponent Reactions in the Heterocyclic Chemistry

    Bo Jiang;Feng Shi;Shu-Jiang Tu

  • Asymmetric Barton–Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons

    Unknown

  • Kröhnke reaction in aqueous media: one-pot clean synthesis of 4′-aryl-2,2′:6′,2″-terpyridines

    Shujiang Tu;Runhong Jia;Bo Jiang;Junyong Zhang

  • Stereoselective synthesis of sulfonated 1-indenones via radical-triggered multi-component cyclization of β-alkynyl propenones

    Zheng-Jia Shen;Ya-Nan Wu;Chun-Lan He;Long He

  • Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations

    Yi Long Zhu;Bo Jiang;Wen Juan Hao;Jiang Kai Qiu

  • An efficient one-pot, three-component synthesis of indeno[1,2-b]quinoline-9,11(6H,10H)-dione, acridine-1,8(2H,5H)-dione and quinoline-3-carbonitrile derivatives from enaminones

    Shu-Jiang Tu;Bo Jiang;Run-Hong Jia;Jun-Yong Zhang

  • A multi-component domino reaction for the direct access to polyfunctionalized indolesvia intermolecular allylic esterification and indolation

    Bo Jiang;Mian-Shuai Yi;Feng Shi;Shu-Jiang Tu

  • A novel synthesis of fluorinated pyrazoles via gold(I)-catalyzed tandem aminofluorination of alkynes in the presence of Selectfluor.

    Unknown

  • Ag/Brønsted Acid Co-Catalyzed Spiroketalization of β-Alkynyl Ketones toward Spiro[chromane-2,1′-isochromene] Derivatives

    Shuai Liu;Xin-Chan Lan;Ke Chen;Wen-Juan Hao

  • An efficient and chemoselective synthesis of N-substituted 2-aminopyridines via a microwave-assisted multicomponent reaction.

    Shujiang Tu;Bo Jiang;Yan Zhang;Runhong Jia

  • Highly selective domino multicyclizations for forming polycyclic fused acridines and azaheterocyclic skeletons.

    Bo Jiang;Xue Wang;Hai-Wei Xu;Man-Su Tu

Frequent Co-Authors

Shu-Jiang Tu
Shu-Jiang Tu Jiangsu Normal University
Guigen Li
Guigen Li Texas Tech University
Feng Shi
Feng Shi Jiangsu Normal University
Xiaohong Zhang
Xiaohong Zhang Soochow University
Hui Wei
Hui Wei Nanjing University
Shun-Jun Ji
Shun-Jun Ji Soochow University
Wei Chen
Wei Chen Jiangnan University

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