World's Best Scientists 2026 revealed!
Shuji Kanemasa

Shuji Kanemasa

D-Index & Metrics

Chemistry

D-Index
45
Citations
7943
World Ranking
16378
National Ranking
1289

Shuji Kanemasa 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 Shuji Kanemasa 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: 393 publications — 79th percentile

79% of scientists in this discipline score the same or lower.

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

Shuji Kanemasa 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 Shuji Kanemasa 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: 45 D-Index — 10th percentile

10% of scientists in this discipline score the same or lower.

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

Overview

Shuji Kanemasa is affiliated with Kyushu University in Japan. Their academic profile includes engagement primarily in research activities associated with this institution.

No specific data is available regarding recent papers by Shuji Kanemasa, including titles, years of publication, or publication venues.

There are no frequent co-authors or collaborative partnerships documented, indicating either independent research work or limited available metadata on collaborations.

Shuji Kanemasa's publication record does not list any recurrent venues for dissemination of research findings, which may suggest either a broad range of publication outlets or a lack of concentrated publication activity in specific journals or conferences.

The scientist has not recorded any book publications linked to particular publishers, nor is there information on the number or scope of such publications.

Information regarding main fields, subfields of study, or primary research topics is not provided, so no specific domains or areas of specialization can be identified within their scholarly profile.

There are no awards or honors listed, which may reflect either a lack of such recognitions or unreported data on these aspects.

Best Publications

  • Highly Enantioselective Catalytic Fluorination and Chlorination Reactions of Carbonyl Compounds Capable of Two‐Point Binding

    Norio Shibata;Junji Kohno;Kazumi Takai;Takehisa Ishimaru

  • Lewis Acid-Catalyzed Enantioselective Hydroxylation Reactions of Oxindoles and β-Keto Esters Using DBFOX Ligand

    Takehisa Ishimaru;Norio Shibata;Jun Nagai;Shuichi Nakamura

  • Transition-Metal Aqua Complexes of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyloxazoline). Effective Catalysis in Diels−Alder Reactions Showing Excellent Enantioselectivity, Extreme Chiral Amplification, and High Tolerance to Water, Alcohols, Amines, and Acids

    Shuji Kanemasa;Yoji Oderaotoshi;Shin Ichi Sakaguchi;Hidetoshi Yamamoto

  • Recent Advances in Azomethine Ylide Chemistry

    Otohiko Tsuge;Shuji Kanemasa

  • Recent advances in synthetic applications of nitrile oxide cycloaddition (1981-1989)

    Shuji Kanemasa;Otohiko Tsuge

  • ASYMMETRIC CONJUGATE ADDITION OF THIOLS TO A 3-(2-ALKENOYL)-2-OXAZOLIDINONE CATALYZED BY THE DBFOX/PH AQUA COMPLEX OF NICKEL(II) PERCHLORATE

    Shuji Kanemasa;and Yoji Oderaotoshi;Eiji Wada

  • Lithium bromide-triethylamine induced cycloaddition of N-alkylidene 2-amino esters and amides to electron-deficient olefins with high regio- and stereoselectivity

    Otohiko Tsuge;Shuji Kanemasa;Manabu Yoshioka

  • Simple generation of nonstabilized azomethine ylides through decarboxylative condensation of α-amino acids with carbonyl compounds via 5-oxazolidinone intermediates

    Otohiko Tsuge;Shuji Kanemasa;Masayuki Ohe;Shigeori Takenaka

  • Highly Endo- and Enantioselective Asymmetric Nitrone Cycloadditions Catalyzed by the Aqua Complex of 4,6-Dibenzofurandiyl-2,2‘-bis(4-phenyl- oxazoline)−Nickel(II) Perchlorate. Transition Structure Based on Dramatic Effect of MS 4A on Selectivities

    Shuji Kanemasa;Yoji Oderaotoshi;Junji Tanaka;Eiji Wada

  • Cationic Aqua Complexes of the C2-Symmetric trans-Chelating Ligand (R,R)-4,6-Dibenzofurandiyl-2,2′-bis(4-phenyloxazoline). Absolute Chiral Induction in Diels-Alder Reactions Catalyzed by Water-Tolerant Enantiopure Lewis Acids

    Shuji Kanemasa;Yoji Oderaotoshi;Hidetoshi Yamamoto;Junji Tanaka

  • Desymmetrization-like catalytic enantioselective fluorination of malonates and its application to pharmaceutically attractive molecules.

    Dhande Sudhakar Reddy;Norio Shibata;Jun Nagai;Shuichi Nakamura

  • Enantioselective Michael Additions of Nitromethane by a Catalytic Double Activation Method Using Chiral Lewis Acid and Achiral Amine Catalysts

    Unknown

  • Chiral DBFOX/Ph complex catalyzed enantioselective nitrone cycloadditions to alpha,beta-unsaturated aldehydes.

    Moto Shirahase;Shuji Kanemasa;Yoji Oderaotoshi

  • Enantioselective Enol Lactone Synthesis under Double Catalytic Conditions

    Unknown

  • Cornerstone works for catalytic 1,3-dipolar cycloaddition reactions

    Shuji Kanemasa

  • A new general route to N-protonated azomethine ylides from N-(silylmethyl)amidines and -thioamides. Cycloaddition of synthetic equivalents of nitrile ylides

    Otohiko Tsuge;Shuji Kanemasa;Koyo Matsuda

  • Lewis acid-catalyzed nitrone cycloadditions to bidentate and tridentate α,β-unsaturated ketones. High rate acceleration, absolutely endo-selective and regioselective reactions

    Shuji Kanemasa;Takashi Uemura;Eiji Wada

  • Regioselective cycloadditions of N-protonated azomethine ylides and 2-azaallyl anions generated from N-(silylmethyl) thioimidates, synthetic equivalents of nonstabilized nitrile ylides

    Otohiko Tsuge;Shuji Kanemasa;Toshiaki Yamada;Koyo Matsuda

  • Enantioselective Michael addition reactions of malononitrile catalyzed by chiral Lewis acid and achiral amine catalysts

    Kennosuke Itoh;Yoji Oderaotoshi;Shuji Kanemasa

  • Stereochemical study on 1,3-dipolar cycloaddition reactions of heteroaromatic N-ylides with unsymmetrically substituted olefinic dipolarophiles

    Otohiko Tsuge;Shuji Kanemasa;Shigeori Takenaka

  • Stereoselectivity of Cydoaddition of N-(Cyanomethyl)- and N-(α-Cyanobenzyl)imines with Olefinic Dipolarophiles. Synthetic Equivalents of Nitrile Ylide 1,3-Dipoles

    Otohiko Tsuge;Kazunori Ueno;Shuji Kanemasa;Kiyotaka Yorozu

  • Synthetic Versatility of N-(Silylmethyl)imines: Water-Induced Generation of N-Protonated Azomethine Ylides of Nonstabilized Type and Fluoride-Induced Generation of 2-Azaallyl Anions

    Otohiko Tsuge;Shuji Kanemasa;Akira Hatada;Koyo Matsuda

Frequent Co-Authors

Dennis P. Curran
Dennis P. Curran University of Pittsburgh
Hideo Nagashima
Hideo Nagashima Kyushu University
Takashi Hayashi
Takashi Hayashi Osaka University

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