T. Yakaiah

634 total citations
23 papers, 530 citations indexed

About

T. Yakaiah is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, T. Yakaiah has authored 23 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Organic Chemistry, 8 papers in Molecular Biology and 1 paper in Pharmacology. Recurrent topics in T. Yakaiah's work include Multicomponent Synthesis of Heterocycles (10 papers), Synthesis and Characterization of Heterocyclic Compounds (7 papers) and Quinazolinone synthesis and applications (6 papers). T. Yakaiah is often cited by papers focused on Multicomponent Synthesis of Heterocycles (10 papers), Synthesis and Characterization of Heterocyclic Compounds (7 papers) and Quinazolinone synthesis and applications (6 papers). T. Yakaiah collaborates with scholars based in India and Pakistan. T. Yakaiah's co-authors include B. Narsaiah, A. Raghu Ram Rao, V. Sridhar, J. Venkateshwara Rao, B. Narsaiah, U. S. N. Murthy, G. Venkat Reddy, K. Pranay Kumar, Balasubramanian Sridhar and T. Parthasarathy and has published in prestigious journals such as Tetrahedron Letters, European Journal of Medicinal Chemistry and Bioorganic & Medicinal Chemistry Letters.

In The Last Decade

T. Yakaiah

23 papers receiving 508 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
T. Yakaiah India 12 509 164 26 16 13 23 530
Frédéric Fabis France 13 453 0.9× 102 0.6× 44 1.7× 44 2.8× 10 0.8× 38 520
N. Suchetha Shetty India 7 523 1.0× 138 0.8× 21 0.8× 21 1.3× 26 2.0× 12 561
A. Raghu Ram Rao India 6 343 0.7× 111 0.7× 16 0.6× 24 1.5× 13 1.0× 19 386
Karen Mollet Belgium 11 330 0.6× 77 0.5× 43 1.7× 19 1.2× 19 1.5× 20 377
Carlos González‐Romero Mexico 11 277 0.5× 100 0.6× 9 0.3× 16 1.0× 25 1.9× 31 321
Arumugasamy Jeevanandam Taiwan 13 351 0.7× 120 0.7× 37 1.4× 20 1.3× 11 0.8× 21 424
Nobuko Mibu Japan 11 308 0.6× 92 0.6× 15 0.6× 12 0.8× 5 0.4× 31 342
Marcello Rasparini Italy 12 312 0.6× 124 0.8× 51 2.0× 9 0.6× 8 0.6× 16 372
Umar Faruk Mansoor United States 8 258 0.5× 99 0.6× 24 0.9× 11 0.7× 6 0.5× 8 332
N Uçartürk Türkiye 5 402 0.8× 140 0.9× 12 0.5× 16 1.0× 6 0.5× 6 441

Countries citing papers authored by T. Yakaiah

Since Specialization
Citations

This map shows the geographic impact of T. Yakaiah's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by T. Yakaiah with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Yakaiah more than expected).

Fields of papers citing papers by T. Yakaiah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T. Yakaiah. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by T. Yakaiah. The network helps show where T. Yakaiah may publish in the future.

Co-authorship network of co-authors of T. Yakaiah

This figure shows the co-authorship network connecting the top 25 collaborators of T. Yakaiah. A scholar is included among the top collaborators of T. Yakaiah based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with T. Yakaiah. T. Yakaiah is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Yakaiah, T., A. Ravi Kumar, G. Sathaiah, et al.. (2012). Synthesis of novel optically pure α-amino acid functionalised-7-trifluoromethyl substituted quinolone derivatives and their antibacterial activity. Medicinal Chemistry Research. 22(1). 186–194. 6 indexed citations
2.
Yakaiah, T., C. Kurumurthy, B. Narsaiah, et al.. (2012). GdCl3 promoted synthesis of novel pyrimidine fused indazole derivatives and their anticancer activity. Medicinal Chemistry Research. 21(12). 4261–4273. 18 indexed citations
3.
Paul, Vincent, et al.. (2010). Efficient Strategy for the Synthesis of 4-Hydroxy-1H-pyrrole-2,3-dicarboxylic Ester Derivatives Using Transition-Metal-Oxide Catalysts. Synthetic Communications. 40(21). 3152–3158. 5 indexed citations
4.
Narsaiah, B., T. Yakaiah, G. Gayatri, et al.. (2010). Synthesis and theoretical studies on energetics of novel N- and O- perfluoroalkyl triazole tagged thienopyrimidines – Their potential as adenosine receptor ligands. European Journal of Medicinal Chemistry. 45(5). 1739–1745. 28 indexed citations
5.
Yakaiah, T., B. Narsaiah, V. Sridhar, et al.. (2009). Synthesis leading to novel 2,4,6-trisubstituted quinazoline derivatives, their antibacterial and cytotoxic activity against THP-1, HL-60 and A375 cell lines. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 48(6). 840–847. 18 indexed citations
6.
Yakaiah, T., G. Gayatri, K. Pranay Kumar, et al.. (2009). Click chemistry: Studies on the synthesis of novel fluorous tagged triazol-4-yl substituted quinazoline derivatives and their biological evaluation – Theoretical and experimental validation. European Journal of Medicinal Chemistry. 45(1). 78–84. 36 indexed citations
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Yakaiah, T., et al.. (2007). Synthesis of novel 4,6-disubstituted quinazoline derivatives, their anti-inflammatory and anti-cancer activity (cytotoxic) against U937 leukemia cell lines☆. European Journal of Medicinal Chemistry. 43(4). 846–852. 199 indexed citations
9.
Yakaiah, T., et al.. (2007). Synthesis and structure–activity relationships of novel pyrimido[1,2-b]indazoles as potential anticancer agents against A-549 cell lines. Bioorganic & Medicinal Chemistry Letters. 17(12). 3445–3453. 68 indexed citations
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Yakaiah, T., et al.. (2006). Gadolinium(III) chloride: a novel and an efficient reagent for the synthesis of homoallylic alcohols. Tetrahedron Letters. 47(26). 4315–4318. 12 indexed citations
14.
Reddy, G. Venkat, et al.. (2006). ZnBr2‐Catalyzed Efficient Oxidative Homo Coupling of Aryl Magnesium Bromides. Synthetic Communications. 36(20). 3079–3084. 7 indexed citations
15.
Yakaiah, T., K. Srinivas, G. Venkat Reddy, et al.. (2006). Regioselective addition of Grignard reagents to 2,6-dicyanoanilines and cyclization to new quinazoline derivatives under thermal/microwave irradiation conditions. Journal of Fluorine Chemistry. 127(3). 351–359. 10 indexed citations
16.
Yakaiah, T., et al.. (2005). ZrOCl 2 .8H 2 O as a new solid phase and recyclable catalyst for an efficient Knoevenagel condensation under solvent- free microwave irradiation conditions. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 44(6). 1301–1303. 6 indexed citations
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Yakaiah, T., et al.. (2005). Silica Sulphuric Acid: An Efficient and Recyclable Catalyst for the Synthesis of β‐Acetamido Ketones in Single Pot. Synthetic Communications. 35(10). 1307–1312. 19 indexed citations
19.
Narsaiah, B., et al.. (2005). Synthesis of New Trifluoromethyl Substituted 11H-Isoindolo[2,1-a]benzimidazol-11-one Derivatives. Heterocycles. 65(10). 2329–2329. 5 indexed citations
20.
Reddy, G. Venkat, et al.. (2004). Efficient and Convenient Method for the Synthesis of Poly Functionalised 4H‐Pyrans. Synthetic Communications. 34(23). 4431–4437. 16 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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