Atul Kumar

482 total citations
20 papers, 402 citations indexed

About

Atul Kumar is a scholar working on Organic Chemistry, Computer Networks and Communications and Molecular Biology. According to data from OpenAlex, Atul Kumar has authored 20 papers receiving a total of 402 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Organic Chemistry, 2 papers in Computer Networks and Communications and 2 papers in Molecular Biology. Recurrent topics in Atul Kumar's work include Catalytic C–H Functionalization Methods (8 papers), Multicomponent Synthesis of Heterocycles (7 papers) and Synthesis and Biological Evaluation (6 papers). Atul Kumar is often cited by papers focused on Catalytic C–H Functionalization Methods (8 papers), Multicomponent Synthesis of Heterocycles (7 papers) and Synthesis and Biological Evaluation (6 papers). Atul Kumar collaborates with scholars based in India, China and Saudi Arabia. Atul Kumar's co-authors include Siddharth Sharma, Qazi Naveed Ahmed, Suman Srivastava, Vishwa Deepak Tripathi, Ram Awatar Maurya, Manish Gupta, Mukesh Kumar, Satyanarayana Battula, Garima Gupta and A. Gupta and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Atul Kumar

20 papers receiving 396 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Atul Kumar India 10 378 72 27 26 11 20 402
Ashoke Deb India 8 534 1.4× 109 1.5× 14 0.5× 52 2.0× 14 1.3× 17 564
Kumkum Kumari India 8 397 1.1× 33 0.5× 24 0.9× 16 0.6× 4 0.4× 19 412
Neil F. Langille United States 9 305 0.8× 61 0.8× 29 1.1× 22 0.8× 10 0.9× 13 335
Mehdi Soheilizad Iran 11 362 1.0× 81 1.1× 19 0.7× 17 0.7× 12 1.1× 25 378
Ravi S. Lamani India 8 322 0.9× 72 1.0× 26 1.0× 12 0.5× 10 0.9× 23 343
Qing‐Lan Pei China 7 405 1.1× 68 0.9× 32 1.2× 52 2.0× 8 0.7× 11 428
Dilipkumar Uredi India 10 367 1.0× 63 0.9× 16 0.6× 44 1.7× 8 0.7× 16 402
Chintalapudi Venkaiah India 9 361 1.0× 85 1.2× 21 0.8× 37 1.4× 6 0.5× 13 375
Raju Adepu India 13 433 1.1× 113 1.6× 58 2.1× 17 0.7× 16 1.5× 26 475
Cherkupally Sanjeeva Reddy India 10 333 0.9× 51 0.7× 27 1.0× 12 0.5× 18 1.6× 35 354

Countries citing papers authored by Atul Kumar

Since Specialization
Citations

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

Fields of papers citing papers by Atul Kumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Atul Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Atul Kumar. A scholar is included among the top collaborators of Atul Kumar 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 Atul Kumar. Atul Kumar 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.
Kumar, Atul, et al.. (2023). TBAI-Catalyzed Regioselective Hydroxyperoxidation of 1-Aryl/Alkyl-1,3-dienes. Organic Letters. 25(23). 4313–4317. 9 indexed citations
2.
Fernandes, Rodney A., Atul Kumar, & Ramdas S. Pathare. (2022). Asymmetric total synthesis of (+)-dihydroitomanallene B and formal synthesis of (−)-kumausallene. Chemical Communications. 58(85). 11921–11924. 2 indexed citations
3.
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5.
Kumar, Atul, J. Carlos Menéndez, Raju Suresh Kumar, et al.. (2021). Synthesis of Fused Quinoline Derivatives from Easily Accessible N ‐(2‐aminobenzylidene)‐4‐methylanilines under Catalyst‐Free Conditions in Water. ChemistrySelect. 6(38). 10436–10439. 1 indexed citations
6.
Kumar, Atul & Vellaisamy Sridharan. (2021). Transition Metal‐Catalyzed Synthesis of 1,2‐Diketones: An Overview. Asian Journal of Organic Chemistry. 10(7). 1619–1637. 9 indexed citations
7.
Kumar, Atul, et al.. (2019). Iodine–DMSO-promoted divergent reactivities of arylacetylenes. Chemical Communications. 55(31). 4511–4514. 46 indexed citations
8.
Kumar, Atul, et al.. (2019). Introducing Oxo-Phenylacetyl (OPAc) as a Protecting Group for Carbohydrates. The Journal of Organic Chemistry. 84(7). 4131–4148. 6 indexed citations
9.
Kumar, Atul, Shahnawaz Khan, & Qazi Naveed Ahmed. (2017). Base-Controlled Reactions through an Aldol Intermediate Formed between 2-Oxoaldehydes and Malonate Half Esters. Organic Letters. 19(18). 4730–4733. 9 indexed citations
10.
Kumar, Atul & Qazi Naveed Ahmed. (2017). A Benzoquinone Imine Assisted Ring‐Opening/Ring‐Closing Strategy of the RCOCHN1N2 System: Dinitrogen Extrusion Reaction to Benzimidazoles. European Journal of Organic Chemistry. 2017(19). 2751–2756. 2 indexed citations
11.
Khan, Shahnawaz, Atul Kumar, Monika Gupta, & Qazi Naveed Ahmed. (2017). The Ritter Reaction of 2‐Oxoaldehydes at Room Temperature: Divergent Behaviour towards Acid Strength.. ChemistrySelect. 2(34). 11336–11340. 9 indexed citations
12.
Kumar, Atul, Narsaiah Battini, Raju Ranjith Kumar, S. Athimoolam, & Qazi Naveed Ahmed. (2016). Air‐Assisted 2‐Oxo‐Driven Dehydrogenative α,α‐Diamination of 2‐Oxo Aldehydes to 2‐Oxo Acetamidines. European Journal of Organic Chemistry. 2016(20). 3344–3348. 7 indexed citations
13.
Battula, Satyanarayana, Atul Kumar, A. Gupta, & Qazi Naveed Ahmed. (2015). 2-Oxo-Driven N2 Elimination Induced Decarbonylative Cyclization Reaction in Benzotriazoles to 6-Aminophenanthridines. Organic Letters. 17(22). 5562–5565. 35 indexed citations
14.
Battula, Satyanarayana, Atul Kumar, & Qazi Naveed Ahmed. (2015). Metal-free oxidative cleavage of the C–C bond in α-hydroxy-β-oxophosphonates. Organic & Biomolecular Chemistry. 13(39). 9953–9956. 10 indexed citations
15.
Kumar, Atul, Veeraruna Kavitha, & N. Hemachandra. (2015). Finite horizon risk sensitive MDP and linear programming. 7826–7831. 5 indexed citations
16.
Kumar, Atul, Veeraruna Kavitha, & N. Hemachandra. (2015). Power constrained DTNs: Risk MDP-LP approach. 35. 154–160. 2 indexed citations
17.
Kumar, Atul, Siddharth Sharma, Vishwa Deepak Tripathi, & Suman Srivastava. (2010). Synthesis of chalcones and flavanones using Julia–Kocienski olefination. Tetrahedron. 66(48). 9445–9449. 93 indexed citations
18.
Kumar, Atul, Siddharth Sharma, & Ram Awatar Maurya. (2009). A novel multi-component reaction of indole, formaldehyde, and tertiary aromatic amines. Tetrahedron Letters. 50(43). 5937–5940. 63 indexed citations
19.
Kumar, Atul, Suman Srivastava, & Garima Gupta. (2009). Supramolecular carbohydrate scaffold-catalyzed synthesis of tetrahydroquinolines. Tetrahedron Letters. 51(3). 517–520. 34 indexed citations
20.
Kumar, Atul, Mukesh Kumar, & Manish Gupta. (2009). An efficient organocatalyzed multicomponent synthesis of diarylmethanes via Mannich type Friedel–Crafts reaction. Tetrahedron Letters. 50(50). 7024–7027. 41 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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