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Discipline name D-Index World Ranking Current World Ranking National Ranking Current National Ranking Publications Citations
Chemistry 46 15935 14373 306 303 665 8847

Balasubramanian Sridhar publications per year

The chart shows the history of publications by Balasubramanian Sridhar between 2001 and 2025, highlighting the no. of papers published in each year and offering an overview of the publication velocity of this scholar. Balasubramanian Sridhar published across 25 years, from 2001 to 2025, averaging 38.1 papers a year. Output peaked at 80 publications in 2015. 65 of the 952 publications appeared in the last two years.

No. of publications
20 40 60 80
Bar chart. Horizontal axis: year, 2001 to 2025. Vertical axis: number of publications, 0 to 80. Peak 80 publications in 2015. 2001: 2 publications 2002: 4 publications 2003: 1 publication 2004: 0 publications 2005: 23 publications 2006: 33 publications 2007: 26 publications 2008: 19 publications 2009: 34 publications 2010: 37 publications 2011: 44 publications 2012: 60 publications 2013: 71 publications 2014: 68 publications 2015: 80 publications 2016: 63 publications 2017: 43 publications 2018: 63 publications 2019: 48 publications 2020: 36 publications 2021: 34 publications 2022: 48 publications 2023: 50 publications 2024: 37 publications 2025: 28 publications
2001 2025

952 publications in total across all disciplines

View publications per year as a table
Balasubramanian Sridhar: publications per year, 2001 to 2025
Year Publications
2001 2
2002 4
2003 1
2004 0
2005 23
2006 33
2007 26
2008 19
2009 34
2010 37
2011 44
2012 60
2013 71
2014 68
2015 80
2016 63
2017 43
2018 63
2019 48
2020 36
2021 34
2022 48
2023 50
2024 37
2025 28
Total 952
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Balasubramanian Sridhar 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 Balasubramanian Sridhar 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, 661–680 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: 665 publications — 95th percentile

95% 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
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 92 665
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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Balasubramanian Sridhar 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 Balasubramanian Sridhar 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: 46 D-Index — 12th percentile

12% 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 46
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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Research.com Recognitions

  • 2001 - IEEE Fellow For advances in computer vision-based obstacle detection and developments in low-altitude helicopter flight.

Overview

Balasubramanian Sridhar is affiliated with the Indian Institute of Chemical Technology in India and has contributed extensively to the fields of chemistry and materials science. Their research output spans both broad and specialized areas with a focus on organic chemistry and materials chemistry.

The scientist's recent publications cover a range of topics, including organic synthesis, crystal packing, nonlinear optical properties, and bioactive molecules. Notable papers include:

  • Visible-light-driven metal-free aerobic synthesis of highly diastereoselective phosphinoylpyrroloindoles, 2020, Organic & Biomolecular Chemistry
  • Influence of crystal packing on the thermal properties of cocrystals and cocrystal solvates of olanzapine: insights from computations, 2020, CrystEngComm
  • Investigation on synthesis, growth, Hirshfeld surface and third order nonlinear optical properties of Urea-Succinic Acid single crystal: A potential candidate for self-defocusing lasing application, 2022, Optical Materials
  • Indole-fused spirochromenes as potential anti-tubercular agents: design, synthesis and in vitro evaluation, 2020, Molecular Diversity
  • Direct Access for the Regio- and Stereoselective Synthesis of N-Alkenylpyrazoles and Chromenopyrazoles, 2021, The Journal of Organic Chemistry

The research areas addressed by Sridhar include key themes such as crystallization and solubility studies, X-ray diffraction in crystallography, and catalytic functionalization methods. Their body of work demonstrates engagement with molecular interactions and synthesis approaches relevant to biological evaluation.

  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Catalytic C-H Functionalization Methods
  • Catalytic Alkyne Reactions
  • Cyclopropane Reaction Mechanisms
  • Crystallography and Molecular Interactions
  • Synthesis and Biological Evaluation

Sridhar collaborates frequently with other researchers in their field. Some of the most common co-authors include Artem O. Surov, German L. Perlovich, Jupally Prashanth, Alexander P. Voronin, and B. V. Subba Reddy.

The scientist's works have appeared repeatedly in several journals, suggesting a consistent publication presence in:

  • The Cambridge Structural Database
  • Organic & Biomolecular Chemistry
  • Tetrahedron Letters
  • Journal of Molecular Structure
  • Organic Letters

The core areas of expertise for Sridhar are chemistry and materials science, with specific emphasis on

  • Organic Chemistry
  • Materials Chemistry
  • Physical and Theoretical Chemistry
  • Molecular Biology
  • Electronic, Optical and Magnetic Materials

Recognition for Sridhar's work includes the IEEE Fellow award in 2001 for contributions related to computer vision-based obstacle detection and developments in low-altitude helicopter flight, indicating interdisciplinary expertise that extends beyond chemistry.

Best Publications

  • Design, Synthesis, and Structure–Activity Correlations of Novel Dibenzo[b,d]furan, Dibenzo[b,d]thiophene, and N-Methylcarbazole Clubbed 1,2,3-Triazoles as Potent Inhibitors of Mycobacterium tuberculosis

    Santhosh Reddy Patpi;Lokesh Pulipati;Perumal Yogeeswari;Dharmarajan Sriram

  • Synthesis of Biosurfactant-Based Silver Nanoparticles with Purified Rhamnolipids Isolated from Pseudomonas aeruginosa BS-161R

    C. Ganesh Kumar;Suman Kumar Mamidyala;Biswanath Das;B. Sridhar

  • Synthesis and biological evaluation of tetrazole containing compounds as possible anticancer agents

    Chebolu Naga Sesha Sai Pavan Kumar;Dusmant Kumar Parida;Amlipur Santhoshi;Anil Kumar Kota

  • A Ligand-Free Pd-Catalyzed Cascade Reaction: An Access to the Highly Diverse Isoquinolin-1(2H)-one Derivatives via Isocyanide and Ugi-MCR Synthesized Amide Precursors

    Vikas Tyagi;Shahnawaz Khan;Archana Giri;Harsh M. Gauniyal

  • Enantioselective nitroaldol (Henry) reaction using copper(II) complexes of (-)-sparteine.

    H. Maheswaran;K. Leon Prasanth;G. Gopi Krishna;K. Ravikumar

  • Facile Assembly of Fused Isoquinolines by Gold(I)-Catalyzed Coupling–Cyclization Reactions between o-Alkynylbenzaldehydes and Aromatic Amines Containing Tethered Nucleophiles

    Nitin T. Patil;Anil Kumar Mutyala;Pediredla G. V. V. Lakshmi;Penmatcha V. K. Raju

  • A flexible enantioselective total synthesis of diospongins A and B and their enantiomers using catalytic hetero-Diels-Alder/Rh-catalyzed 1,4-addition and asymmetric transfer hydrogenation reactions as key steps.

    Gullapalli Kumaraswamy;Gajula Ramakrishna;Bharatam Jagadeesh

  • Highly efficient, mild and chemo- and stereoselective synthesis of enaminones and enamino esters using silica supported perchloric acid under solvent-free conditions

    Biswanath Das;Katta Venkateswarlu;Anjoy Majhi;Majjigapu Ravinder Reddy

  • Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.

    Yalla Kiran Kumar;Gadi Ranjith Kumar;Thota Jagadeshwar Reddy;Balasubramanian Sridhar

  • Synthesis, anticancer activity and photophysical properties of novel substituted 2-oxo-2H-chromenylpyrazolecarboxylates.

    J. Ashok Kumar;G. Saidachary;G. Mallesham;B. Sridhar

  • Gold-Catalyzed Intramolecular Cyclization of N-Propargylic β-Enaminones for the Synthesis of 1,4-Oxazepine Derivatives.

    Kommuru Goutham;Desamala Ashok Kumar;Surisetti Suresh;Balasubramanian Sridhar

  • Synthesis of new chromeno-annulated cis-fused pyrano[3,4-c]pyran derivatives via domino Knoevenagel–hetero-Diels–Alder reactions and their biological evaluation towards antiproliferative activity

    A. Venkatesham;R. Srinivasa Rao;K. Nagaiah;J. S. Yadav

  • Usnic Acid Enaminone-Coupled 1,2,3-Triazoles as Antibacterial and Antitubercular Agents.

    Pavan K Bangalore;Siva K Vagolu;Rakesh K Bollikanda;Dileep K Veeragoni

  • First example of quinine-squaramide catalyzed enantioselective addition of diphenyl phosphite to ketimines derived from isatins

    Unknown

  • Synthesis and antitubercular evaluation of novel dibenzo[b,d]furan and 9-methyl-9H-carbazole derived hexahydro-2H-pyrano[3,2-c]quinolines via Povarov reaction.

    Srinivas Kantevari;Thirumal Yempala;Govardhan Surineni;Balasubramanian Sridhar

  • Relay Catalytic Branching Cascade: A Technique to Access Diverse Molecular Scaffolds

    Nitin T Patil;Valmik S Shinde;Balasubramanian Sridhar

  • Cu(OTf)2-catalyzed synthesis of 2,3-disubstituted indoles and 2,4,5-trisubstituted pyrroles from α-diazoketones.

    B. V. Subba Reddy;M. Ramana Reddy;Y. Gopal Rao;J. S. Yadav

  • Substrate Directed C–H Activation for the Synthesis of Benzo[c]cinnolines through a Sequential C–C and C–N Bond Formation

    Unknown

  • Facile Diversity-Oriented Synthesis and Antitubercular Evaluation of Novel Aryl and Heteroaryl Tethered Pyridines and Dihydro-6H-quinolin-5-ones Derived via Variants of the Bohlmann–Rahtz Reaction

    Srinivas Kantevari;Santhosh Reddy Patpi;Dinesh Addla;Siddamal Reddy Putapatri

  • Synthesis of highly substituted 2-perfluoroalkyl quinolines by electrophilic iodocyclization of perfluoroalkyl propargyl imines/amines.

    Pravin R. Likhar;Madavu Salian Subhas;Sarabindu Roy;Mannepalli Lakshmi Kantam

  • Au(I)-Catalyzed Cascade Reaction Involving Formal Double Hydroamination of Alkynes Bearing Tethered Carboxylic Groups: An Easy Access to Fused Dihydrobenzimidazoles and Tetrahydroquinazolines

    Nitin T. Patil;Anil Kumar Mutyala;Pediredla G. V. V. Lakshmi;Balakrishna Gajula

  • Synthesis, crystal structure and antidiabetic activity of substituted (E)-3-(Benzo [d]thiazol-2-ylamino) phenylprop-2-en-1-one.

    Vijay S. Patil;Kamalakar P. Nandre;Sougata Ghosh;Vaidya Jayathirtha Rao

  • Second- and third-order nonlinear optical and quantum chemical studies on 2-amino-4-picolinium-nitrophenolate-nitrophenol: A phasematchable organic single crystal

    Unknown

  • Tandem Prins/Friedel–Crafts cyclization for stereoselective synthesis of heterotricyclic systems.

    B V Subba Reddy;Prashant Borkar;J S Yadav;B Sridhar

  • "On water" expedient synthesis of 3-indolyl-3-hydroxy oxindole derivatives and their anticancer activity in vitro.

    Parvathaneni Sai Prathima;Pamanji Rajesh;Janapala Venkateswara Rao;Uppalapati Sai Kailash

  • Iron-Catalyzed Regioselective Direct Oxidative Aryl–Aryl Cross-Coupling

    Unknown

Frequent Co-Authors

Jhillu S. Yadav
Jhillu S. Yadav Indian Institute of Chemical Technology
Nitin T. Patil
Nitin T. Patil Indian Institute of Science Education and Research, Bhopal
Dharmarajan Sriram
Dharmarajan Sriram Birla Institute of Technology and Science, Pilani
Biswanath Das
Biswanath Das Indian Institute of Chemical Technology
Perumal Yogeeswari
Perumal Yogeeswari Birla Institute of Technology and Science, Pilani
B. V. Subba Reddy
B. V. Subba Reddy Council of Scientific and Industrial Research
Srivari Chandrasekhar
Srivari Chandrasekhar Indian Institute of Chemical Technology
Bojja Sreedhar
Bojja Sreedhar Indira Gandhi Centre for Atomic Research
Michael G. B. Drew
Michael G. B. Drew University of Reading
Antonio Frontera
Antonio Frontera University of the Balearic Islands

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