World's Best Scientists 2026 revealed!
Deevi Basavaiah

Deevi Basavaiah

D-Index & Metrics

Chemistry

D-Index
44
Citations
10305
World Ranking
16669
National Ranking
324

Deevi Basavaiah 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 Deevi Basavaiah 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: 202 publications — 33rd percentile

33% of scientists in this discipline score the same or lower.

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

Deevi Basavaiah 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 Deevi Basavaiah 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: 44 D-Index — 7th percentile

7% of scientists in this discipline score the same or lower.

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

Overview

Deevi Basavaiah is affiliated with the University of Hyderabad in India and works primarily in the field of Materials Science. Their research emphasizes Materials Chemistry and Organic Chemistry, contributing notably to crystallization and solubility studies as well as X-ray diffraction in crystallography.

The scientist's recent publications include a mix of experimental and synthetic chemistry topics. Among them is a 2022 article titled An umpolung strategy for intermolecular [2 + 2 + 1] cycloaddition of aryl aldehydes and nitriles: a facile access to 2,4,5-trisubstituted oxazoles published in Chemical Science. This work involves synthetic methodology related to cycloaddition reactions.

Basavaiah has also contributed to multiple entries in The Cambridge Structural Database in 2022, documenting experimental crystal structures. These publications serve as foundational data for crystallographic studies.

The scientist's main topics of research cover:

  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Cyclopropane Reaction Mechanisms
  • N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
  • Catalytic C-H Functionalization Methods

Basavaiah frequently collaborates with fellow researchers including Gangadhararao Golime, Shivalal Banoth, and Saidulu Todeti, each having coauthored seven papers with them.

The primary venues where Basavaiah publishes are:

  • The Cambridge Structural Database
  • Chemical Science

Best Publications

  • Recent Advances in the Baylis−Hillman Reaction and Applications

    Deevi Basavaiah;and Anumolu Jaganmohan Rao;Tummanapalli Satyanarayana

  • THE BAYLIS-HILLMAN REACTION : A NOVEL CARBON-CARBON BOND FORMING REACTION

    Deevi Basavaiah;Polisetti Dharma Rao;Rachakonda Suguna Hyma

  • Recent contributions from the Baylis-Hillman reaction to organic chemistry.

    Deevi Basavaiah;Bhavanam Sekhara Reddy;Satpal Singh Badsara

  • The Baylis–Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry

    Deevi Basavaiah;Kalapala Venkateswara Rao;Raju Jannapu Reddy

  • The Baylis–Hillman reaction: a novel concept for creativity in chemistry

    Deevi Basavaiah;Gorre Veeraraghavaiah

  • Simple and one-pot protocol for synthesis of indene-spiro-oxindoles involving tandem Prins and Friedel-Crafts reactions.

    Deevi Basavaiah;Kanumuri Ramesh Reddy

  • A Facile One-Pot Conversion of Acetates of the Baylis−Hillman Adducts to [E]-α-Methylcinnamic Acids

    Deevi Basavaiah;Marimganti Krishnamacharyulu;Rachakonda Suguna Hyma;Pakala K. S. Sarma

  • A new protocol for the syntheses of (E)-3-benzylidenechroman-4-ones: a simple synthesis of the methyl ether of bonducellin

    Deevi Basavaiah;Manickam Bakthadoss

  • Baylis–Hillman chemistry: a novel synthesis of functionalized 1,4-pentadienes

    Deevi Basavaiah;Nagaswamy Kumaragurubaran;Duddu S Sharada

  • A simple synthesis of α-methylene-β-hydroxyalkanones

    D. Basavaiah;V.V.L. Gowriswari

  • The Baylis-HillmanBromides as Versatile Synthons: A Facile One-Pot Synthesisof Indolizine and Benzofused Indolizine Frameworks

    Deevi Basavaiah;Badugu Devendar;Dandamudi V. Lenin;Tummanapalli Satyanarayana

  • First example of electrophile induced Baylis–Hillman reaction: a novel facile one-pot synthesis of indolizine derivatives

    Deevi Basavaiah;Anumolu Jaganmohan Rao

  • Applications of Baylis–Hillman acetates: one-pot, facile and convenient synthesis of substituted γ-lactams

    Deevi Basavaiah;Jamjanam Srivardhana Rao

  • DABCO catalyzed dimerization of α,β-unsaturated ketones and nitriles

    D. Basavaiah;V.V.L. Gowriswari;T.K. Bharathi

  • The Baylis−Hillman Reaction: One-Pot Facile Synthesis of 2,4-Functionalized 1,4-Pentadienes

    Deevi Basavaiah;Duddu S. Sharada;Nagaswamy Kumaragurubaran;Ravi Mallikarjuna Reddy

  • Applications of Baylis–Hillman chemistry: one-pot convenient synthesis of functionalized (1H)-quinol-2-ones and quinolines

    Deevi Basavaiah;Ravi Mallikarjuna Reddy;Nagaswamy Kumaragurubaran;Duddu S Sharada

  • The Baylis–Hillman reaction: a new continent in organic chemistry – our philosophy, vision and over three decades of research

    Deevi Basavaiah;Ram Tilak Naganaboina

  • Applications of the Baylis–Hillman reaction 2: a simple stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes

    Deevi Basavaiah;Pakala K. S. Sarma;Anagani K. D. Bhavani

  • A novel and facile synthesis of functionalized [4.4.3] and [4.4.4]propellano-bislactones using acetates of the Baylis-Hillman adducts.

    Deevi Basavaiah;Tummanapalli Satyanarayana

  • Chiral acrylates as substrates in baylis-hillman reaction

    D. Basavaiah;V.V.L. Gowriswari;P.K.S. Sarma;P. Dharma Rao

  • A novel, tandem construction of C–N and C–C bonds: facile and one-pot transformation of the Baylis–Hillman adducts into 2-benzazepines

    Deevi Basavaiah;Tummanapalli Satyanarayana

Frequent Co-Authors

Herbert C. Brown
Herbert C. Brown Purdue University West Lafayette
Ei-ichi Negishi
Ei-ichi Negishi Purdue University West Lafayette

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