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Morris J. Robins

D-Index & Metrics

Chemistry

D-Index
70
Citations
14228
World Ranking
6013
National Ranking
1830

Morris J. Robins 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 Morris J. Robins 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: 371 publications — 76th percentile

76% of scientists in this discipline score the same or lower.

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

Morris J. Robins 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 Morris J. Robins 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: 70 D-Index — 68th percentile

68% of scientists in this discipline score the same or lower.

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

Overview

Morris J. Robins is affiliated with Brigham Young University in the United States. Their research spans multiple fields including Chemistry, Energy, and Medicine. Within these broader disciplines, their work particularly focuses on specialized subfields such as Inorganic Chemistry, Renewable Energy, Sustainability and the Environment, as well as Oncology.

The main topics covered in Morris J. Robins's research include Metal-Catalyzed Oxygenation Mechanisms, Metalloenzymes and iron-sulfur proteins, and Metal complexes synthesis and properties.

Their publication record includes articles in recognized scientific venues. One recent paper is titled "Model Substrate/Inactivation Reactions for MoaA and Ribonucleotide Reductases: Loss of Bromo, Chloro, or Tosylate Groups from C2 of 1,5-Dideoxyhomoribofuranoses upon Generation of an α-Oxy Radical at C3", published in 2020 in the journal Molecules.

Frequent collaborators in their research include:

  • Stanislaw F. Wnuk
  • Mukesh M. Mudgal
  • Ireneusz Nowak

Their publications have appeared notably in:

  • Molecules

Best Publications

  • Nucleic acid related compounds. 42. A general procedure for the efficient deoxygenation of secondary alcohols. Regiospecific and stereoselective conversion of ribonucleosides to 2'-deoxynucleosides

    Morris J. Robins;John S. Wilson;Fritz Hansske

  • Smooth and efficient deoxygenation of secondary alcohols. A general procedure for the conversion of ribonucleosides to 2'-deoxynucleosides

    Morris J. Robins;John S. Wilson

  • NUCLEIC ACID RELATED COMPOUNDS. 39. EFFICIENT CONVERSION OF 5-IODO TO 5-ALKYNYL AND DERIVED 5-SUBSTITUTED URACIL BASES AND NUCLEOSIDES

    Morris J. Robins;Philip J. Barr

  • 2'-Deoxy-2'-methylenecytidine and 2'-deoxy-2',2'-difluorocytidine 5'-diphosphates: potent mechanism-based inhibitors of ribonucleotide reductase.

    C. H. Baker;J. Banzon;J. M. Bollinger;J. Stubbe

  • Removal of silyl protecting groups from hydroxyl functions with ammonium fluoride in methanol

    Weijian Zhang;Morris J. Robins

  • Purine Nucleosides. XI. The Synthesis of 2'-Deoxy-9-α- and -β-D-ribofuranosylpurines and the Correlation of Their Anomeric Structure with Proton Magnetic Resonance Spectra1

    Morris J. Robins;Roland K. Robins

  • Nucleic acid related compounds. 37. Convenient and high-yield syntheses of N-[(2-hydroxyethoxy)methyl] heterocycles as "acyclic nucleoside" analogues

    Morris J. Robins;Peter W. Hatfield

  • Cerium(IV)-mediated halogenation at C-5 of uracil derivatives

    Junichi Asakura;Morris J. Robins

  • N-6-(delta-3-isopentenyl) adenosine. A component of the transfer ribonucleic acid of yeast and of mammalian tissue, methods of isolation, and characterization.

    Morris J. Robins;Ross H. Hall;Roosevelt Thedford

  • Nucleic acid related compounds. 40. Synthesis and biological activities of 5-alkynyluracil nucleosides.

    Erik De Clercq;Johan Descamps;Jan Balzarini;Jerzy Giziewicz

  • Nucleic acid related compounds. 33. Conversions of adenosine and guanosine to 2,6-dichloro, 2-amino-6-chloro, and derived purine nucleosides

    Morris J. Robins;Bogdan Uznański

  • The role of the 5'-hydroxyl group of adenosine in determining substrate specificity for adenosine deaminase.

    Alexander. Bloch;Morris J. Robins;James R. McCarthy

  • Isolation of N6-(γ,γ-Dimethylallyl)adenosine from Soluble Ribonucleic Acid1

    Ross H. Hall;Morris J. Robins;Lubomyr Stasiuk;Roosevelt Thedford

  • Synthesis and biological activity of selected 2,6-disubstituted-(2-deoxy- -and- -D-erythro-pentofuranosyl)purines.

    Leon F. Christensen;Arthur D. Broom;Morris J. Robins;Alexander Bloch

  • Nucleic acid related compounds. 34. Non-aqueous diazotization with tert-butyl nitrite. Introduction of fluorine, chlorine, and bromine at C-2 of purine nucleosides

    Morris J. Robins;Bogdan Uznański

  • High-yield regioselective synthesis of 9-glycosyl guanine nucleosides and analogues via coupling with 2-N-acetyl-6-O-diphenylcarbamoylguanine

    Ruiming Zou;Morris J. Robins

  • Carbon-13 magnetic resonance. XIV. Aza-analogs of polycyclic aromatic hydrocarbons

    Ronald J. Pugmire;David M. Grant;Morris J. Robins;Roland K. Robins

  • Azoles as Suzuki cross-coupling leaving groups: syntheses of 6-arylpurine 2'-deoxynucleosides and nucleosides from 6-(imidazol-1-yl)- and 6-(1,2,4-triazol-4-yl)purine derivatives.

    Jiangqiong Liu;Morris J. Robins

  • Nucleic acid related compounds. 12. The facile and high-yield stannous chloride catalyzed monomethylation of the cis-glycol system of nucleosides by diazomethane.

    Morris J. Robins;S. R. Naik;Alan S. K. Lee

  • Nucleic acid related compounds. 13

    Unknown

  • Nucleic Acid Related Compounds. 93. A Solution for the Historic Problem of Regioselective Sugar−Base Coupling To Produce 9-Glycosylguanines or 7-Glycosylguanines1

    Morris J. Robins;Ruiming Zou;Zhiqiang Guo;Stanislaw F. Wnuk

  • 2' And 3'-ketonucleosides and their arabino and xylo reduction products: Convenient access via selective protection and oxidation of ribonucleosides☆

    Unknown

Frequent Co-Authors

Roland K. Robins
Roland K. Robins University of Utah
Jan Balzarini
Jan Balzarini KU Leuven
Ronald T. Borchardt
Ronald T. Borchardt University of Kansas
Erik De Clercq
Erik De Clercq Rega Institute for Medical Research
Carol E. Cass
Carol E. Cass University of Alberta
Roger A. Jones
Roger A. Jones Rutgers, The State University of New Jersey
Malcolm Maccoss
Malcolm Maccoss MSD (United States)
James D. Young
James D. Young University of Alberta
Philip J. Barr
Philip J. Barr BayMedica, Inc.
JoAnne Stubbe
JoAnne Stubbe MIT

External Links

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Best Scientists Citing Morris J. Robins

Jan Balzarini

Jan Balzarini

KU Leuven

Publications: 83

Frank Seela

Frank Seela

University of Münster

Publications: 58

Erik De Clercq

Erik De Clercq

Rega Institute for Medical Research

Publications: 57

Carol E. Cass

Carol E. Cass

University of Alberta

Publications: 53

JoAnne Stubbe

JoAnne Stubbe

MIT

Publications: 41

Jyoti Chattopadhyaya

Jyoti Chattopadhyaya

Uppsala University

Publications: 40

Piet Herdewijn

Piet Herdewijn

KU Leuven

Publications: 37

Roland K. Robins

Roland K. Robins

University of Utah

Publications: 32

Graciela Andrei

Graciela Andrei

KU Leuven

Publications: 30

Phillip Dan Cook

Phillip Dan Cook

Ionis Pharmaceuticals (United States)

Publications: 29

Robert Snoeck

Robert Snoeck

KU Leuven

Publications: 28

James D. Young

James D. Young

University of Alberta

Publications: 27

Wolfgang Pfleiderer

Wolfgang Pfleiderer

University of Konstanz

Publications: 27

Raymond F. Schinazi

Raymond F. Schinazi

Emory University

Publications: 23

Leroy B. Townsend

Leroy B. Townsend

University of Michigan–Ann Arbor

Publications: 21

Akira Matsuda

Akira Matsuda

Juntendo University

Publications: 21

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