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Chihiro Kibayashi

Chihiro Kibayashi

University of Tokyo
Japan

D-Index & Metrics

Chemistry

D-Index
49
Citations
6597
World Ranking
15012
National Ranking
1171

Chihiro Kibayashi 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 Chihiro Kibayashi 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: 279 publications — 58th percentile

58% of scientists in this discipline score the same or lower.

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

Chihiro Kibayashi 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 Chihiro Kibayashi 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: 49 D-Index — 19th percentile

19% of scientists in this discipline score the same or lower.

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

Overview

Chihiro Kibayashi is affiliated with the University of Tokyo in Japan. Their academic profile is characterized by research contributions tied to this institution.

At present, there are no specific records of recent papers, frequent co-authors, or publication venues commonly associated with their work. Likewise, there is no available information regarding book publications or detailed lists of main fields, subfields, or main topics of study.

There is also no publicly recorded information on awards received by Chihiro Kibayashi.

This lack of detailed publication or citation data suggests that either the scientist's work is emerging in the academic community or records are not currently available in the accessible databases. The affiliation with a major research university such as the University of Tokyo indicates involvement in a research environment with opportunities for scientific inquiry and scholarly activities.

Further details about their areas of specialization, research impact, and collaborative networks remain unspecified based on the present dataset.

Best Publications

  • DNA damage by fasicularin

    Sanjay Dutta;Hideki Abe;Sakae Aoyagi;Chihiro Kibayashi

  • First Total Synthesis of the Marine Alkaloids (±)-Fasicularin and (±)-Lepadiformine Based on Stereocontrolled Intramolecular Acylnitroso-Diels−Alder Reaction

    Hideki Abe;and Sakae Aoyagi;Chihiro Kibayashi

  • Total synthesis of (+)-nojirimycin and (+)-1-deoxynojirimycin

    Hideo Iida;Naoki Yamazaki;Chihiro Kibayashi

  • Total synthesis of (-)-incarvilline, (+)-incarvine C, and (-)-incarvillateine.

    Masaya Ichikawa;Masaki Takahashi;Sakae Aoyagi;Chihiro Kibayashi

  • Intramolecular cyclization of enaminones involving arylpalladium complexes. Synthesis of carbazoles

    Hideo Iida;Yoshifumi Yuasa;Chihiro Kibayashi

  • Asymmetric synthesis with α,β-bis[(methoxymethyl)oxy] ketones. Enantioselective total synthesis of natural (+)-indolizidine 195B (bicyclic gephyrotoxin 195B) and (-)-pinidine and their enantiomers from a common chiral synthon

    Naoki Yamazaki;Chihiro Kibayashi

  • Total synthesis of the tricyclic marine alkaloids (-)-lepadiformine, (+)-cylindricine c, and (-)-fasicularin via a common intermediate formed by formic acid-induced intramolecular conjugate azaspirocyclization.

    Hideki Abe;Sakae Aoyagi;Chihiro Kibayashi

  • Enantioselective total synthesis of (+)-negamycin and (−)-epinegamycin by an asymmetric 1,3-dipolar cycloaddition

    Hideo. Iida;Katsura. Kasahara;Chihiro. Kibayashi

  • Asymmetric total synthesis of (+)-negamycin and (−)-3-epinegamycin via enantioselective 1,3-dipolar cycloaddition

    Katsura Kasahara;Hideo Iida;Chihiro Kibayashi

  • Enantiogenic total syntheses of (-)-indolizidines (bicyclic gephyrotoxins) 205A, 207A, 209B, and 235B via the intramolecular Diels-Alder reaction of a chiral N-acylnitroso compound

    Yuji Shishido;Chihiro Kibayashi

  • New Chiral Route to (-)-Swainsonine via an Aqueous Acylnitroso Cycloaddition Approach

    Masaichi Naruse;Sakae Aoyagi;Chihiro Kibayashi

  • Total synthesis of (.+-.)-dihydropinidine, (.+-.)-monomorine I, and (.+-.)-indolizidine 223AB (gephyrotoxin 223AB) by intramolecular nitroso Diels-Alder reaction

    Yohya Watanabe;Hideo Iida;Chihiro Kibayashi

  • Total synthesis of the marine alkaloids (-)-lepadins a, b, and c based on stereocontrolled intramolecular acylnitroso-Diels-Alder reaction.

    Tetsuji Ozawa;Sakae Aoyagi;Chihiro Kibayashi

  • Asymmetric synthesis of 2-substituted pyrrolidines and piperidines by nucleophilic addition to N-acyliminium ions bearing pyrrolidine chiral auxiliaries

    Hideaki Suzuki;Sakae Aoyagi;Chihiro Kibayashi

  • Enantioselective total synthesis of (+)-azimine and (+)-carpaine.

    Taro Sato;Sakae Aoyagi;Chihiro Kibayashi

  • TOTAL SYNTHESIS OF (-)-EPIBATIDINE USING AN ASYMMETRIC DIELS-ALDER REACTION WITH A CHIRAL N-ACYLNITROSO DIENOPHILE

    Sakae Aoyagi;Ryuta Tanaka;Masaichi Naruse;Chihiro Kibayashi

  • STEREOSPECIFIC TOTAL SYNTHESIS OF (.+-.)-GEPHYROTOXIN 223AB

    Hideo Iida;Yohya Watanabe;Chihiro Kibayashi

  • Highly stereoselective total syntheses of (+)-allopumiliotoxins 267A and 339A via intramolecular nickel(II)/chromium(II)-mediated cyclization

    Sakae Aoyagi;Tzu Chueh Wang;Chihiro Kibayashi

  • Enantioselective Allylation of Aldehydes with (Dialkoxyallyl)chromium(III) Complexes.

    Kazuyuki Sugimoto;Sakae Aoyagi;Chihiro Kibayashi

  • Development of new synthetic methods and its application to total synthesis of nitrogen-containing bioactive natural products

    Chihiro Kibayashi

Frequent Co-Authors

Hideki Abe
Hideki Abe National Institute for Materials Science
Tetsuji Kametani
Tetsuji Kametani Tohoku University
John W. Daly
John W. Daly National Institutes of Health
Andrew B. Holmes
Andrew B. Holmes University of Melbourne
Kent S. Gates
Kent S. Gates University of Missouri

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Related Online Degrees & Career Pathways

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