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Ahmad Reza Moosavi-Zare

Ahmad Reza Moosavi-Zare

D-Index & Metrics

Discipline name D-Index World Ranking Current World Ranking National Ranking Current National Ranking Publications Citations
Chemistry 47 15816 14269 121 120 187 6152

Ahmad Reza Moosavi-Zare publications per year

The chart shows the history of publications by Ahmad Reza Moosavi-Zare between 2008 and 2025, highlighting the no. of papers published in each year and offering an overview of the publication velocity of this scholar. Ahmad Reza Moosavi-Zare published across 18 years, from 2008 to 2025, averaging 11.5 papers a year. Output peaked at 25 publications in 2015. 10 of the 207 publications appeared in the last two years.

No. of publications
5 10 15 20 25
Bar chart. Horizontal axis: year, 2008 to 2025. Vertical axis: number of publications, 0 to 25. Peak 25 publications in 2015. 2008: 3 publications 2009: 8 publications 2010: 9 publications 2011: 4 publications 2012: 18 publications 2013: 22 publications 2014: 22 publications 2015: 25 publications 2016: 23 publications 2017: 10 publications 2018: 12 publications 2019: 6 publications 2020: 14 publications 2021: 7 publications 2022: 10 publications 2023: 4 publications 2024: 6 publications 2025: 4 publications
2008 2025

207 publications in total across all disciplines

View publications per year as a table
Ahmad Reza Moosavi-Zare: publications per year, 2008 to 2025
Year Publications
2008 3
2009 8
2010 9
2011 4
2012 18
2013 22
2014 22
2015 25
2016 23
2017 10
2018 12
2019 6
2020 14
2021 7
2022 10
2023 4
2024 6
2025 4
Total 207
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Ahmad Reza Moosavi-Zare 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 Ahmad Reza Moosavi-Zare 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, 181–200 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: 187 publications — 28th percentile

28% 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 1,344 187
201–220 1,281
221–240 1,216
241–260 1,100
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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Ahmad Reza Moosavi-Zare 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 Ahmad Reza Moosavi-Zare 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, 46–47 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: 47 D-Index — 14th percentile

14% 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 47
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
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

Ahmad Reza Moosavi-Zare is affiliated with Bu-Ali Sina University in Iran and has an extensive publication record primarily in the field of Chemistry, with a strong focus on Organic Chemistry. Their research encompasses a variety of specialized topics including multicomponent synthesis of heterocycles, synthesis and biological activity, synthesis and characterization of heterocyclic compounds, synthesis and biological evaluation, microwave-assisted synthesis and applications, chemical synthesis and reactions, and synthesis of organic compounds.

Among recent publications where Moosavi-Zare is a contributing author are:

  • Nano-Co-[4-chlorophenyl-salicylaldimine-pyranopyrimidine dione]Cl2 as a new Schiff base complex and catalyst for the one-pot synthesis of some 4H-pyrimido[2,1-b]benzazoles, 2020, Research on Chemical Intermediates
  • Design of 2-Carboxy-1-sulfopyridin-1-ium Chloride as an Efficient and Eco-friendly Catalyst for the One-pot Synthesis of Highly Functionalized Tetrahydropyridines, 2020, Organic Preparations and Procedures International

Other relevant papers in their recent work include those led by coauthors:

  • Nano-[Fe3O4@SiO2/N-propyl-1-(thiophen-2-yl)ethanimine][ZnCl2] as a nano magnetite Schiff base complex and heterogeneous catalyst for the synthesis of pyrimido[4,5-b]quinolones, 2022, RSC Advances
  • Synthesis of 4,4'-(Aryl Methylene)Bis(3-Methyl-1H-Pyrazol-5-ol) Derivatives and Pyrano[2, 3-c] Pyrazole Derivatives Using an Engineered Copper-Based Nano-Magnetic Catalyst (Fe3O4@SiO2/Si(OEt)(CH2)3NH/CC/EDA/Cu(OAc)2), 2022, Polycyclic aromatic compounds
  • Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst, 2022, ACS Omega

Their frequent co-authors include:

  • Hamid Goudarziafshar
  • Zahra Jalilian
  • Ardeshir Khazaei
  • Soheila Esmaili
  • Mohammad Rezaei-Gohar

Moosavi-Zare's work is often published in several key venues, including:

  • RSC Advances
  • Research on Chemical Intermediates
  • Polycyclic aromatic compounds
  • Organic Preparations and Procedures International
  • ACS Omega

Best Publications

  • Rapid synthesis of 1-amidoalkyl-2-naphthols over sulfonic acid functionalized imidazolium salts

    Mohammad Ali Zolfigol;Ardeshir Khazaei;Ahmad Reza Moosavi-Zare;Abdolkarim Zare

  • Ionic liquid triethylamine-bonded sulfonic acid {[Et3N–SO3H]Cl} as a novel, highly efficient and homogeneous catalyst for the synthesis of β-acetamido ketones, 1,8-dioxo-octahydroxanthenes and 14-aryl-14H-dibenzo[a,j]xanthenes

    Abdolkarim Zare;Ahmad Reza Moosavi-Zare;Maria Merajoddin;Mohammad Ali Zolfigol

  • Design of ionic liquid 3-methyl-1-sulfonic acid imidazolium nitrate as reagent for the nitration of aromatic compounds by in situ generation of NO 2 in acidic media

    Mohammad A. Zolfigol;Ardeshir Khazaei;Ahmad R. Moosavi-Zare;Abdolkarim Zare

  • Ionic Liquid 3-Methyl-1-sulfonic Acid Imidazolium Chloride as a Novel and Highly Efficient Catalyst for the Very Rapid Synthesis of bis(Indolyl)methanes under Solvent-free Conditions

    Mohammad Ali Zolfigol;Ardeshir Khazaei;Ahmad Reza Moosavi-Zare;Abdolkarim Zare

  • A highly stable and active magnetically separable Pd nanocatalyst in aqueous phase heterogeneously catalyzed couplings

    Mohammad Ali Zolfigol;Vahid Khakyzadeh;Ahmad Reza Moosavi-Zare;Abed Rostami

  • Design, characterization and application of new ionic liquid 1-sulfopyridinium chloride as an efficient catalyst for tandem Knoevenagel–Michael reaction of 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one with aldehydes

    Ahmad Reza Moosavi-Zare;Mohammad Ali Zolfigol;Mahmoud Zarei;Abdolkarim Zare

  • Preparation of various xanthene derivatives over sulfonic acid functionalized imidazolium salts (SAFIS) as novel, highly efficient and reusable catalysts

    Mohammad Ali Zolfigol;Vahid Khakyzadeh;Ahmad Reza Moosavi-Zare;Abdolkarim Zare

  • Synthesis of pyranopyrazoles using isonicotinic acid as a dual and biological organocatalyst

    Mohammad Ali Zolfigol;Mahsa Tavasoli;Ahmad Reza Moosavi-Zare;Parvin Moosavi

  • Organocatalyst trityl chloride efficiently promoted the solvent-free synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-ones by in situ formation of carbocationic system in neutral media

    Ardeshir Khazaei;Mohammad Ali Zolfigol;Ahmad Reza Moosavi-Zare;Abdolkarim Zare

  • Magnetic core–shell titanium dioxide nanoparticles as an efficient catalyst for domino Knoevenagel–Michael-cyclocondensation reaction of malononitrile, various aldehydes and dimedone

    Ardeshir Khazaei;Fatemeh Gholami;Vahid Khakyzadeh;Ahmad Reza Moosavi-Zare

  • Synthesis, characterization and application of ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient catalyst for the preparation of hexahydroquinolines

    Abdolkarim Zare;Fereshteh Abi;Ahmad Reza Moosavi-Zare;Mohammad Hassan Beyzavi

  • Synthesis, characterization and application of ZnFe2O4 nanoparticles as a heterogeneous ditopic catalyst for the synthesis of pyrano[2,3-d] pyrimidines

    Ardeshir Khazaei;Azam Ranjbaran;Fatemeh Abbasi;Marzieh Khazaei

  • Ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate: a novel and highly efficient catalyst for the preparation of 1-carbamatoalkyl-2-naphthols and 1-amidoalkyl-2-naphthols

    Abdolkarim Zare;Tahereh Yousofi;Ahmad Reza Moosavi-Zare

  • Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature

    Ardeshir Khazaei;Mohammad Ali Zolfigol;Ahmad Reza Moosavi-Zare;Abdolkarim Zare

  • 3-Methyl-1-Sulfonic acid imidazolium chloride as a new, efficient and recyclable catalyst and solvent for the preparation of N-sulfonyl imines at room temperature

    M. A. Zolfigol;A. Khazaei;A. R. Moosavi-Zare;A. Zare

  • Discovery of an in situ carbocationic system using trityl chloride as a homogeneous organocatalyst for the solvent-free condensation of β-naphthol with aldehydes and amides/thioamides/alkyl carbamates in neutral media

    Ardeshir Khazaei;Mohammad Ali Zolfigol;Ahmad Reza Moosavi-Zare;Fereshteh Abi

  • Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid

    Ahmad Reza Moosavi-Zare;Mohammad Ali Zolfigol;Omid Khaledian;Vahid Khakyzadeh

  • Synthesis of 6-amino-4-(4-methoxyphenyl)-5-cyano-3-methyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazoles using disulfonic acid imidazolium chloroaluminate as a dual and heterogeneous catalyst

    Ahmad Reza Moosavi-Zare;Mohammad Ali Zolfigol;Ehsan Noroozizadeh;Mahsa Tavasoli

  • Preparation of 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1H-pyrazol-5-ol)s over 1,3-disulfonic acid imidazolium tetrachloroaluminate as a novel catalyst

    Ardeshir Khazaei;Mohammad Ali Zolfigol;Ahmad Reza Moosavi-Zare;Zhila Asgari

  • Design of ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate as a dual-catalyst for the one-pot multi-component synthesis of 1,2,4,5-tetrasubstituted imidazoles

    Mohammad Ali Zolfigol;Ardeshir Khazaei;Ahmad Reza Moosavi-Zare;Abdolkarim Zare

  • Design of Ionic Liquid 3‐Methyl‐1‐sulfonic Acid Imidazolium Nitrate as Reagent for the Nitration of Aromatic Compounds by in situ Generation of NO2 in Acidic Media.

    Mohammad A. Zolfigol;Ardeshir Khazaei;Ahmad R. Moosavi‐Zare;Abdolkarim Zare

Frequent Co-Authors

Mohammad Ali Zolfigol
Mohammad Ali Zolfigol Bu-Ali Sina University
Mohammad Norouzi
Mohammad Norouzi Google (United States)
Rafael Luque
Rafael Luque King Saud University
Sadegh Rostamnia
Sadegh Rostamnia Iran University of Science and Technology
Nasser Iranpoor
Nasser Iranpoor Shiraz University
Christoph Böttcher
Christoph Böttcher Freie Universität Berlin
Abbas Afkhami
Abbas Afkhami Bu-Ali Sina University

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