Ashok Kumar Jaladi

646 total citations
30 papers, 543 citations indexed

About

Ashok Kumar Jaladi is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Ashok Kumar Jaladi has authored 30 papers receiving a total of 543 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Organic Chemistry, 14 papers in Inorganic Chemistry and 8 papers in Molecular Biology. Recurrent topics in Ashok Kumar Jaladi's work include Asymmetric Hydrogenation and Catalysis (14 papers), Organoboron and organosilicon chemistry (12 papers) and Advanced Synthetic Organic Chemistry (7 papers). Ashok Kumar Jaladi is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (14 papers), Organoboron and organosilicon chemistry (12 papers) and Advanced Synthetic Organic Chemistry (7 papers). Ashok Kumar Jaladi collaborates with scholars based in South Korea, India and Japan. Ashok Kumar Jaladi's co-authors include B. China Raju, Duk Keun An, Gannerla Saidachary, Ashok Kumar Tiwari, Amtul Z. Ali, Balasubramanian Sridhar, Madhusudana Kuncha, Sachin B. Agawane, Hyun Tae Kim and Hyonseok Hwang and has published in prestigious journals such as Tetrahedron, Molecules and RSC Advances.

In The Last Decade

Ashok Kumar Jaladi

29 papers receiving 535 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ashok Kumar Jaladi South Korea 13 480 142 104 92 31 30 543
Beyhan Yığıt Türkiye 14 502 1.0× 102 0.7× 228 2.2× 144 1.6× 13 0.4× 42 677
Gopal Bose Germany 15 602 1.3× 211 1.5× 97 0.9× 61 0.7× 10 0.3× 24 680
Cam‐Van T. Vo Vietnam 10 607 1.3× 94 0.7× 207 2.0× 44 0.5× 27 0.9× 15 735
Lukas Brieger Germany 12 405 0.8× 72 0.5× 136 1.3× 60 0.7× 12 0.4× 34 539
Murat Yiğit Türkiye 15 506 1.1× 100 0.7× 228 2.2× 143 1.6× 13 0.4× 40 652
Rendy Kartika United States 16 587 1.2× 53 0.4× 116 1.1× 46 0.5× 10 0.3× 39 664
Harish Holla India 14 526 1.1× 107 0.8× 116 1.1× 35 0.4× 5 0.2× 42 616
K. Mukkanti India 13 527 1.1× 92 0.6× 195 1.9× 54 0.6× 7 0.2× 63 667
Venu Srinivas India 16 536 1.1× 156 1.1× 103 1.0× 21 0.2× 7 0.2× 32 670
Afsaneh Zonouzi Iran 14 562 1.2× 68 0.5× 77 0.7× 224 2.4× 8 0.3× 53 731

Countries citing papers authored by Ashok Kumar Jaladi

Since Specialization
Citations

This map shows the geographic impact of Ashok Kumar Jaladi'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 Ashok Kumar Jaladi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ashok Kumar Jaladi more than expected).

Fields of papers citing papers by Ashok Kumar Jaladi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ashok Kumar Jaladi. 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 Ashok Kumar Jaladi. The network helps show where Ashok Kumar Jaladi may publish in the future.

Co-authorship network of co-authors of Ashok Kumar Jaladi

This figure shows the co-authorship network connecting the top 25 collaborators of Ashok Kumar Jaladi. A scholar is included among the top collaborators of Ashok Kumar Jaladi 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 Ashok Kumar Jaladi. Ashok Kumar Jaladi 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
2.
Kim, Hyun Tae, et al.. (2023). Magnesium-mediated hydroboration under ambient condition: A reduction of esters, aldehydes, and ketones. Tetrahedron. 142. 133500–133500. 8 indexed citations
3.
Lee, Ji Hye, et al.. (2023). Grignard Reagent-Catalyzed Hydroboration of Esters, Nitriles, and Imines. Molecules. 28(20). 7090–7090. 5 indexed citations
4.
Kim, Hyun Tae, Jae‐Ho Kim, Ji Hye Lee, et al.. (2022). Effective Magnesium‐catalyzed Hydroboration of Nitriles and Imines. Asian Journal of Organic Chemistry. 11(10). 4 indexed citations
5.
Jaladi, Ashok Kumar, et al.. (2020). Catalyst-free and solvent-free hydroboration of alkynes. New Journal of Chemistry. 44(32). 13626–13632. 24 indexed citations
6.
Jaladi, Ashok Kumar, et al.. (2019). Lithium diisobutyl-tert-butoxyaluminum hydride (LDBBA) catalyzed hydroboration of alkynes and imines with pinacolborane. New Journal of Chemistry. 43(42). 16524–16529. 22 indexed citations
7.
Jaladi, Ashok Kumar, et al.. (2019). Lithium tert‐Butoxide‐catalyzed Hydroboration of Carbonyl Compounds. Bulletin of the Korean Chemical Society. 40(10). 971–975. 15 indexed citations
8.
Jaladi, Ashok Kumar, et al.. (2019). Catalytic Hydroboration of Aldehydes, Ketones, and Alkenes Using Potassium Carbonate: A Small Key to Big Transformation. ACS Omega. 4(14). 15893–15903. 49 indexed citations
9.
Kim, Hyun Tae, et al.. (2018). Suspension Polymerization of Thermally Expandable Microspheres Using Cinnamonitrile and Diethyl Fumarate as Crosslinking Agents. Bulletin of the Korean Chemical Society. 40(1). 45–50. 3 indexed citations
10.
Jaladi, Ashok Kumar, et al.. (2018). Copper diisobutyl-t-butoxyaluminum hydride: A novel reagent for chemoselective reduction of tertiary amides over esters. Tetrahedron Letters. 59(24). 2335–2340. 4 indexed citations
12.
Kim, Joo Yeon, et al.. (2018). Chemoselective reduction of aldehydes and ketones by potassium diisobutyl-t-butoxy aluminum hydride (PDBBA). Tetrahedron. 74(31). 4236–4241. 6 indexed citations
13.
Yang, Su Jin, et al.. (2018). n‐Butyllithium (1 mol %)‐catalyzed Hydroboration of Aldehydes and Ketones with Pinacolborane. Bulletin of the Korean Chemical Society. 40(1). 34–38. 17 indexed citations
15.
Kang, Seung Kyu, Kwan‐Young Jung, Ashok Kumar Jaladi, et al.. (2014). Synthesis and biological evaluation of thienopyrimidine derivatives as GPR119 agonists. Bioorganic & Medicinal Chemistry Letters. 24(17). 4281–4285. 10 indexed citations
16.
Jaladi, Ashok Kumar, Gannerla Saidachary, Mallesham Godumala, et al.. (2013). Synthesis, anticancer activity and photophysical properties of novel substituted 2-oxo-2H-chromenylpyrazolecarboxylates. European Journal of Medicinal Chemistry. 65. 389–402. 75 indexed citations
17.
Jaladi, Ashok Kumar, Ashok Kumar Tiwari, Gannerla Saidachary, et al.. (2013). Pancreatic α-amylase inhibition and free radical scavenging activity of substituted pyranochromenone derivatives. Medicinal Chemistry Research. 23(6). 2821–2833. 6 indexed citations
18.
Jaladi, Ashok Kumar, Ashok Kumar Tiwari, Gannerla Saidachary, et al.. (2013). New Convenient Approach for the Synthesis of Benzyl 2H-Chromenones and their α-Amylase Inhibitory, ABTS.+ Scavenging Activities. Medicinal Chemistry. 9(6). 806–811. 7 indexed citations
19.
Jaladi, Ashok Kumar, et al.. (2009). New antihyperglycemic, α-glucosidase inhibitory, and cytotoxic derivatives of benzimidazoles. Journal of Enzyme Inhibition and Medicinal Chemistry. 25(1). 80–86. 23 indexed citations
20.
Raju, B. China, Ashok Kumar Tiwari, Ashok Kumar Jaladi, et al.. (2009). α-Glucosidase inhibitory antihyperglycemic activity of substituted chromenone derivatives. Bioorganic & Medicinal Chemistry. 18(1). 358–365. 97 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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