World's Best Scientists 2026 revealed!

D-Index & Metrics

Discipline name D-Index World Ranking Current World Ranking National Ranking Current National Ranking Publications Citations
Chemistry 65 7812 7086 54 51 243 12445

Yonggui Robin Chi publications per year

The chart shows the history of publications by Yonggui Robin Chi between 2004 and 2021, highlighting the no. of papers published in each year and offering an overview of the publication velocity of this scholar. Yonggui Robin Chi published across 18 years, from 2004 to 2021, averaging 9.2 papers a year. Output peaked at 27 publications in 2021. 48 of the 165 publications appeared in the last two years.

No. of publications
5 10 15 20 25
Bar chart. Horizontal axis: year, 2004 to 2021. Vertical axis: number of publications, 0 to 27. Peak 27 publications in 2021. 2004: 1 publication 2005: 4 publications 2006: 2 publications 2007: 0 publications 2008: 4 publications 2009: 3 publications 2010: 0 publications 2011: 6 publications 2012: 9 publications 2013: 15 publications 2014: 12 publications 2015: 7 publications 2016: 7 publications 2017: 14 publications 2018: 12 publications 2019: 21 publications 2020: 21 publications 2021: 27 publications
2004 2021

165 publications in total across all disciplines

View publications per year as a table
Yonggui Robin Chi: publications per year, 2004 to 2021
Year Publications
2004 1
2005 4
2006 2
2007 0
2008 4
2009 3
2010 0
2011 6
2012 9
2013 15
2014 12
2015 7
2016 7
2017 14
2018 12
2019 21
2020 21
2021 27
Total 165
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Yonggui Robin Chi 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 Yonggui Robin Chi sits on this spectrum.

No. of scientists
250 500 750 1,000 1,250
Bar chart with 63 bars. Horizontal axis: publications, 61–80 to 1,295+. Vertical axis: number of scientists, 0 to 1,350. Most scientists, 1,350, have 161–180 publications. The last bar groups every scientist with 1,295 publications or more. The highlighted bar, 241–260 publications, is where this scientist sits. 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
61–80 publications 1,295+

This scientist: 243 publications — 47th percentile

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

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

View publications distribution as a table
Number of Chemistry scientists by publication count, Research.com 2026 ranking edition. Based on 17,934 ranked scientists.
Publications Scientists This scientist
61–80 66
81–100 302
101–120 623
121–140 918
141–160 1,218
161–180 1,350
181–200 1,344
201–220 1,281
221–240 1,216
241–260 1,100 243
261–280 979
281–300 939
301–320 764
321–340 643
341–360 628
361–380 522
381–400 459
401–420 397
421–440 327
441–460 270
461–480 265
481–500 252
501–520 201
521–540 185
541–560 148
561–580 148
581–600 132
601–620 114
621–640 104
641–660 91
661–680 92
681–700 73
701–720 57
721–740 54
741–760 67
761–780 45
781–800 46
801–820 39
821–840 32
841–860 36
861–880 29
881–900 26
901–920 24
921–940 14
941–960 23
961–980 28
981–1,000 15
1,001–1,020 29
1,021–1,040 12
1,041–1,060 19
1,061–1,080 12
1,081–1,100 6
1,101–1,120 8
1,121–1,140 12
1,141–1,160 5
1,161–1,180 6
1,181–1,200 14
1,201–1,220 7
1,221–1,240 2
1,241–1,260 6
1,261–1,280 4
1,281–1,294 6
1,295+ 100
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Yonggui Robin Chi 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 Yonggui Robin Chi sits on this spectrum.

No. of scientists
250 500 750 1,000
Bar chart with 61 bars. Horizontal axis: D-Index, 40–41 to 159+. Vertical axis: number of scientists, 0 to 1,051. Most scientists, 1,051, have 56–57 D-Index. The last bar groups every scientist with 159 D-Index or more. The highlighted bar, 64–65 D-Index, is where this scientist sits. 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
40–41 D-Index 159+

This scientist: 65 D-Index — 58th percentile

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

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

View D-Index distribution as a table
Number of Chemistry scientists by D-index, Research.com 2026 ranking edition. Based on 17,934 ranked scientists.
D-Index Scientists This scientist
40–41 289
42–43 612
44–45 808
46–47 776
48–49 835
50–51 861
52–53 872
54–55 933
56–57 1,051
58–59 930
60–61 882
62–63 834
64–65 731 65
66–67 775
68–69 683
70–71 646
72–73 561
74–75 501
76–77 437
78–79 388
80–81 354
82–83 292
84–85 275
86–87 254
88–89 235
90–91 185
92–93 192
94–95 155
96–97 163
98–99 125
100–101 105
102–103 105
104–105 112
106–107 88
108–109 68
110–111 69
112–113 65
114–115 79
116–117 61
118–119 44
120–121 37
122–123 40
124–125 33
126–127 26
128–129 34
130–131 35
132–133 25
134–135 27
136–137 17
138–139 16
140–141 20
142–143 20
144–145 15
146–147 9
148–149 9
150–151 16
152–153 11
154–155 9
156–157 3
158 3
159+ 98
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Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Aldehyde

Yonggui Robin Chi mostly deals with Catalysis, Organic chemistry, Carbene, Enantioselective synthesis and Organocatalysis. His work investigates the relationship between Catalysis and topics such as Combinatorial chemistry that intersect with problems in Single bond. Yonggui Robin Chi has researched Carbene in several fields, including Cycloaddition, Surface modification, Stereochemistry, Trifluoromethyl and Nucleophile.

Brønsted–Lowry acid–base theory is closely connected to Electrophile in his research, which is encompassed under the umbrella topic of Nucleophile. His Enantioselective synthesis research focuses on subjects like Isatin, which are linked to Steric effects, Benzoin and Chemoselectivity. The various areas that Yonggui Robin Chi examines in his Organocatalysis study include Aldehyde, Michael reaction, HOMO/LUMO, Ketone and Enone.

His most cited work include:

  • A family of metal-organic frameworks exhibiting size-selective catalysis with encapsulated noble-metal nanoparticles. (257 citations)
  • Oxidative γ-addition of enals to trifluoromethyl ketones: enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis. (243 citations)
  • β-Carbon activation of saturated carboxylic esters through N -heterocyclic carbene organocatalysis (168 citations)

What are the main themes of his work throughout his whole career to date?

His main research concerns Catalysis, Carbene, Enantioselective synthesis, Combinatorial chemistry and Organic chemistry. In Catalysis, Yonggui Robin Chi works on issues like Molecule, which are connected to Lactone and Functional group. The Carbene study combines topics in areas such as Surface modification, Organocatalysis, Carbon and Medicinal chemistry.

His work carried out in the field of Enantioselective synthesis brings together such families of science as Iminium, Nucleophilic addition, Annulation and Imine. His Combinatorial chemistry study also includes fields such as

  • Kinetic resolution and related Acylation,
  • Heteroatom most often made with reference to Moiety. His work on Electrophile, Ketone, Stereoisomerism and Diels alder as part of general Organic chemistry study is frequently linked to Oxidative phosphorylation, therefore connecting diverse disciplines of science.

He most often published in these fields:

  • Catalysis (119.48%)
  • Carbene (106.06%)
  • Enantioselective synthesis (57.58%)

What were the highlights of his more recent work (between 2019-2021)?

  • Catalysis (119.48%)
  • Carbene (106.06%)
  • Combinatorial chemistry (63.64%)

In recent papers he was focusing on the following fields of study:

His primary scientific interests are in Catalysis, Carbene, Combinatorial chemistry, Enantioselective synthesis and Medicinal chemistry. His Catalysis research includes elements of Steric effects and Polymer chemistry. Yonggui Robin Chi has included themes like Organocatalysis, Cycloaddition, Annulation and Nucleophilic addition in his Carbene study.

His Combinatorial chemistry study combines topics from a wide range of disciplines, such as Kinetic resolution, Molecule, Chirality, Addition reaction and Stereoselectivity. His Enantioselective synthesis research is multidisciplinary, incorporating elements of Lactam, Heteroatom, Aldol reaction, Allene and Aryl. His work in the fields of Organic chemistry, such as Amination, overlaps with other areas such as Component.

Between 2019 and 2021, his most popular works were:

  • Prediction of NHC-catalyzed chemoselective functionalizations of carbonyl compounds: a general mechanistic map (15 citations)
  • A Glycosylated Cationic Block Poly(β-peptide) Reverses Intrinsic Antibiotic Resistance in All ESKAPE Gram-Negative Bacteria. (14 citations)
  • Gold and Carbene Relay Catalytic Enantioselective Cycloisomerization/Cyclization Reactions of Ynamides and Enals (13 citations)

In his most recent research, the most cited papers focused on:

  • Organic chemistry
  • Catalysis
  • Aldehyde

Yonggui Robin Chi spends much of his time researching Combinatorial chemistry, Carbene, Catalysis, Enantioselective synthesis and Electrophile. His Combinatorial chemistry study integrates concerns from other disciplines, such as Indoline, Cascade reaction, Palladium and Stereoselectivity. His Carbene study incorporates themes from Organocatalysis, Reactive intermediate, Nucleophile and Homogeneous catalysis.

Catalysis and Rapid access are two areas of study in which he engages in interdisciplinary work. His biological study spans a wide range of topics, including Lactam, Transition metal, Cycloisomerization, Metal and Bicyclic molecule. His Electrophile study necessitates a more in-depth grasp of Organic chemistry.

Best Publications

  • A family of metal-organic frameworks exhibiting size-selective catalysis with encapsulated noble-metal nanoparticles.

    Weina Zhang;Guang Lu;Chenlong Cui;Yayuan Liu

  • Oxidative γ-addition of enals to trifluoromethyl ketones: enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis.

    Junming Mo;Xingkuan Chen;Yonggui Robin Chi

  • One-pot multi-component asymmetric cascade reactions catalyzed by soluble star polymers with highly branched non-interpenetrating catalytic cores.

    Yonggui Chi;Steven T Scroggins;Jean M J Fréchet

  • N‐Heterocyclic Carbene Organocatalysis: Activation Modes and Typical Reactive Intermediates

    Xingkuan Chen;Hongling Wang;Zhichao Jin;Yonggui Robin Chi;Yonggui Robin Chi

  • β-Carbon activation of saturated carboxylic esters through N -heterocyclic carbene organocatalysis

    Zhenqian Fu;Jianfeng Xu;Tingshun Zhu;Wendy Wen Yi Leong

  • N-heterocyclic carbene-catalyzed [3+4] cycloaddition and kinetic resolution of azomethine imines

    Ming Wang;Zhijian Huang;Jianfeng Xu;Yonggui Robin Chi

  • NHC Organocatalytic Formal LUMO Activation of α,β‐Unsaturated Esters for Reaction with Enamides

    Jiajia Cheng;Zhijian Huang;Yonggui Robin Chi

  • Functionalization of Benzylic C(sp3)H Bonds of Heteroaryl Aldehydes through N‐Heterocyclic Carbene Organocatalysis

    Xingkuan Chen;Song Yang;Bao-An Song;Yonggui Robin Chi

  • Carbene-Catalyzed Asymmetric Construction of Atropisomers.

    Runjiang Song;Yongtao Xie;Zhichao Jin;Yonggui Robin Chi

  • Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts.

    Lin Hao;Yu Du;Hui Lv;Xingkuan Chen

  • Highly enantioselective addition of enals to isatin-derived ketimines catalyzed by N-heterocyclic carbenes: synthesis of spirocyclic γ-lactams.

    Hui Lv;Bhoopendra Tiwari;Junming Mo;Chong Xing

  • Enantioselective Organocatalytic Aminomethylation of Aldehydes: A Role for Ionic Interactions and Efficient Access to β2-Amino Acids

    Yonggui Chi;Samuel H. Gellman

  • Benzene construction via organocatalytic formal [3+3] cycloaddition reaction

    Tingshun Zhu;Pengcheng Zheng;Chengli Mou;Song Yang

  • N-heterocyclic carbene-catalyzed radical reactions for highly enantioselective β-hydroxylation of enals.

    Yuexia Zhang;Yu Du;Zhijian Huang;Jianfeng Xu

  • Enantioselective Organocatalytic Michael Addition of Aldehydes to Nitroethylene: Efficient Access to γ2-Amino Acids

    Yonggui Chi;Li Guo;Nathan A. Kopf;Samuel H. Gellman

  • Stereospecific Synthesis of Conformationally Constrained γ-Amino Acids: New Foldamer Building Blocks That Support Helical Secondary Structure

    Li Guo;Yonggui Chi;Aaron M. Almeida;Ilia A. Guzei

  • Enantioselective Oxidative Cross-Dehydrogenative Coupling of Tertiary Amines to Aldehydes**

    Junmin Zhang;Bhoopendra Tiwari;Chong Xing;Xingkuan Chen

  • Organocatalytic Enantioselective γ-Aminoalkylation of Unsaturated Ester: Access to Pipecolic Acid Derivatives

    Jianfeng Xu;Zhichao Jin;Yonggui Robin Chi

  • Direct β‐Activation of Saturated Aldehydes to Formal Michael Acceptors through Oxidative NHC Catalysis

    Junming Mo;Liang Shen;Yonggui Robin Chi

  • Access to P-Stereogenic Phosphinates via N-Heterocyclic Carbene-Catalyzed Desymmetrization of Bisphenols

    Zhijian Huang;Xuan Huang;Baosheng Li;Chengli Mou

  • Enantioselective Organocatalytic Michael Additions of Aldehydes to Enones

    T. J. Peelen;Y. Chi;S. H. Gellman

Frequent Co-Authors

Song Yang
Song Yang Guizhou University
Baoan Song
Baoan Song Guizhou University
Bin Liu
Bin Liu National University of Singapore
Richard D. Webster
Richard D. Webster Nanyang Technological University
Jun Sun
Jun Sun Singapore Management University
Rakesh Ganguly
Rakesh Ganguly Nanyang Technological University
Fengwei Huo
Fengwei Huo Nanjing Tech University
Yun-Dong Wu
Yun-Dong Wu Peking University
Mary B. Chan-Park
Mary B. Chan-Park Nanyang Technological University
Guillermo C. Bazan
Guillermo C. Bazan National University of Singapore

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