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Jae Nyoung Kim

D-Index & Metrics

Chemistry

D-Index
51
Citations
9188
World Ranking
13957
National Ranking
267

Jae Nyoung Kim 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 Jae Nyoung Kim 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: 428 publications — 83rd percentile

83% of scientists in this discipline score the same or lower.

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

Jae Nyoung Kim 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 Jae Nyoung Kim 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: 51 D-Index — 23rd percentile

23% of scientists in this discipline score the same or lower.

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

Overview

Jae Nyoung Kim is affiliated with Chonnam National University in South Korea. Their research is primarily concentrated in the field of Chemistry, with a strong focus on Organic Chemistry. Additional subfields of study include Molecular Biology, Pharmaceutical Science, and Plant Science.

Kim's published work encompasses various topics related to synthetic organic chemistry and chemical synthesis. Key research themes include:

  • Asymmetric Synthesis and Catalysis
  • Synthetic Organic Chemistry Methods
  • Sulfur-Based Synthesis Techniques
  • Chemical synthesis and alkaloids
  • Advanced Synthetic Organic Chemistry
  • Fluorine in Organic Chemistry
  • Biological Activity of Diterpenoids and Biflavonoids

The scientist's recent publications appear predominantly in the Bulletin of the Korean Chemical Society and Synthetic Communications. Specific papers include:

  • "Synthesis of Spirooxindoles Bearing 1,3-Oxathiolane-2-thione Moiety From Isatin-Derived Propargylic Alcohols" (2021), Bulletin of the Korean Chemical Society
  • "Synthesis of five-ring-fused azepinone derivatives from bis-isatins via sequential 6π-electrocyclic ring closure, ring expansion, and dehydrogenation process" (2023), Bulletin of the Korean Chemical Society
  • "One-pot synthesis of spirooxindoles bearing α-methylene-γ-butyrolactone moiety from Morita-Baylis-Hillman carbonates of isatins and paraformaldehyde" (2024), Bulletin of the Korean Chemical Society
  • "Total synthesis of agastaquinone, a diterpenoid quinone isolated from Agastache rugosa" (2020), Synthetic Communications

Frequent collaborators in Kim's research include Sangku Lee, Junseong Lee, Yoo Jisu, Jae-Kyung Jung, and Myeong Sik Yoon. Sangku Lee and Junseong Lee are notable for multiple co-authorships with Kim.

Best Publications

  • Regioselective synthesis of 1,3,4,5-tetrasubstituted pyrazoles from Baylis–Hillman adducts

    Ka Young Lee;Jeong Mi Kim;Jae Nyoung Kim

  • Baylis-Hillman reaction and chemical transformations of Baylis-Hillman adducts

    Ka Young Lee;Saravanan Gowrisankar;Jae Nyoung Kim

  • Recent advances in the Pd-catalyzed chemical transformations of Baylis–Hillman adducts

    Saravanan Gowrisankar;Hyun Seung Lee;Sung Hwan Kim;Ka Young Lee

  • Synthesis of 3-quinolinecarboxylic acid esters from the Baylis–Hillman adducts of 2-halobenzaldehyde N-tosylimines

    Jae Nyoung Kim;Hong Jung Lee;Ka Young Lee;Hyoung Shik Kim

  • Synthesis of enantiomerically enriched Baylis–Hillman alcohols from their acetates: combination of kinetic resolution during the salt formation with (DHQD)2PHAL and following asymmetric induction during hydrolysis with NaHCO3 as a water surrogate

    Jae Nyoung Kim;Hong Jung Lee;Ji Hyeon Gong

  • Synthesis of N-substituted 1,4-dihydroquinolines from the Baylis–Hillman acetates via the successive SN2′–SNAr isomerization strategy

    Jae Nyoung Kim;Hyoung Shik Kim;Ji Hyeon Gong;Yun Mi Chung

  • Synthesis of 3-ethoxycarbonyl-4-hydroxyquinoline N-oxides from the Baylis-Hillman adducts of o-nitrobenzaldehydes

    Jae Nyoung Kim;Ka Young Lee;Hyoung Shik Kim;Tae Yi Kim

  • Facile synthesis of 2H-indazole derivatives starting from the Baylis–Hillman adducts of 2-cyclohexen-1-one

    Ka Young Lee;Saravanan Gowrisankar;Jae Nyoung Kim

  • Synthesis of quinolines from the Baylis–Hillman acetates via the oxidative cyclization of sulfonamidyl radical as the key step

    Jae Nyoung Kim;Yun Mi Chung;Yang Jin Im

  • An efficient Pd-catalyzed hydration of nitrile with acetaldoxime

    Eun Sun Kim;Hoo Sook Kim;Jae Nyoung Kim

  • Highly efficient Pd-catalyzed synthesis of nitriles from aldoximes

    Hoo Sook Kim;Sung Hwan Kim;Jae Nyoung Kim

  • Regioselective allylic amination of the Baylis-Hillman adducts: An easy and practical access to the Baylis-Hillman adducts of N-tosylimines

    Jae Nyoung Kim;Hong Jung Lee;Ka Young Lee;Ji Hyeon Gong

  • Facile synthesis of α,β-acetylenic ketones and 2,5-disubstituted furans : consecutive activation of triple and double bond with ZnBr2 toward the synthesis of furan ring

    Ka Young Lee;Mi Jung Lee;Jae Nyoung Kim

  • Synthesis of 6-oxacyclopropa[a]indene derivatives starting from Baylis-Hillman adducts via Pd-mediated C(sp3)-H activation

    Hoo Sook Kim;Saravanan Gowrisankar;Sung Hwan Kim;Jae Nyoung Kim

  • Synthesis of 3-substituted-4-hydroxyquinoline N-oxides from the Baylis–Hillman adducts of o-nitrobenzaldehydes

    Ka Young Lee;Jeong Mi Kim;Jae Nyoung Kim

  • An efficient InCl3-catalyzed hydration of nitriles to amides: acetaldoxime as an effective water surrogate

    Eun Sun Kim;Hyun Seung Lee;Sung Hwan Kim;Jae Nyoung Kim

  • An expedient synthesis of 2-substituted naphthalenes from the Baylis–Hillman adducts

    Jae Nyoung Kim;Yang Jin Im;Ji Hyeon Gong;Ka Young Lee

  • Synthesis of ethyl 3-cyano-2-methylcinnamates and 3-cyano-2-methylcinnamonitriles from the Baylis–Hillman acetates

    Yun Mi Chung;Ji Hyeon Gong;Taek Hyeon Kim;Jae Nyoung Kim

  • Chemical transformation of Baylis-Hillman adducts: The reaction of methyl 3-arylamino-2-methylene-3-phenylpropanoates in polyphosphoric acid

    Chang Gon Lee;Ka Young Lee;Sangku Lee;Jae Nyoung Kim

  • Regioselective ortho-hydroxylation of aryl moiety of 2-arylpyridines using Pd(OAC)2/Oxone in PEG-3400/tert-BuOH

    Sung Hwan Kim;Hyun Seung Lee;Se Hee Kim;Jae Nyoung Kim

Frequent Co-Authors

Jin Yong Lee
Jin Yong Lee Sungkyunkwan University
Kwangmeyung Kim
Kwangmeyung Kim Korea Institute of Science and Technology
Song Yub Shin
Song Yub Shin Chosun University
Shim Sung Lee
Shim Sung Lee Gyeongsang National University

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Best Scientists Citing Jae Nyoung Kim

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Xiao-Feng Wu

Xiao-Feng Wu

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Publications: 21

Ying‐Chun Chen

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Publications: 15

Irishi N. N. Namboothiri

Irishi N. N. Namboothiri

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Publications: 14

Min Shi

Min Shi

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Publications: 13

Shi-Kai Tian

Shi-Kai Tian

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Publications: 12

Jhillu S. Yadav

Jhillu S. Yadav

Indian Institute of Chemical Technology

Publications: 12

Bhisma K. Patel

Bhisma K. Patel

Indian Institute of Technology Guwahati

Publications: 9

Helfried Neumann

Helfried Neumann

Leibniz Institute for Catalysis

Publications: 9

Bao-Xiang Zhao

Bao-Xiang Zhao

Shandong University

Publications: 8

Choon-Hong Tan

Choon-Hong Tan

Nanyang Technological University

Publications: 8

Yin Wei

Yin Wei

Chinese Academy of Sciences

Publications: 8

Matthias Beller

Matthias Beller

Leibniz Institute for Catalysis

Publications: 8

Mahmoud Nasrollahzadeh

Mahmoud Nasrollahzadeh

University of Qom

Publications: 8

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Vladimir Gevorgyan

The University of Texas at Dallas

Publications: 8

Fangjun Huo

Fangjun Huo

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Publications: 8

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