Rajendra K. Mallick

484 total citations
20 papers, 425 citations indexed

About

Rajendra K. Mallick is a scholar working on Organic Chemistry, Pharmaceutical Science and Process Chemistry and Technology. According to data from OpenAlex, Rajendra K. Mallick has authored 20 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 1 paper in Pharmaceutical Science and 1 paper in Process Chemistry and Technology. Recurrent topics in Rajendra K. Mallick's work include Catalytic Alkyne Reactions (14 papers), Catalytic C–H Functionalization Methods (11 papers) and Cyclopropane Reaction Mechanisms (10 papers). Rajendra K. Mallick is often cited by papers focused on Catalytic Alkyne Reactions (14 papers), Catalytic C–H Functionalization Methods (11 papers) and Cyclopropane Reaction Mechanisms (10 papers). Rajendra K. Mallick collaborates with scholars based in India, France and United Kingdom. Rajendra K. Mallick's co-authors include Akhila K. Sahoo, Vincent Gandon, Shubham Dutta, B. Prabagar, Rajeshwer Vanjari, Shengwen Yang, Sanatan Nayak, Jonathan Clayden, Arnaud Voituriez and Maria Schwarz and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Rajendra K. Mallick

19 papers receiving 421 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rajendra K. Mallick India 12 410 33 22 22 9 20 425
Abhisek Joshi India 10 435 1.1× 43 1.3× 32 1.5× 16 0.7× 9 1.0× 17 450
Xueling Mo China 11 333 0.8× 39 1.2× 23 1.0× 27 1.2× 13 1.4× 14 351
Zongbin Jia China 8 289 0.7× 52 1.6× 24 1.1× 28 1.3× 13 1.4× 13 324
Shubham Dutta India 15 545 1.3× 53 1.6× 23 1.0× 30 1.4× 9 1.0× 27 568
Jiang‐Ling Shi China 12 368 0.9× 49 1.5× 25 1.1× 33 1.5× 8 0.9× 16 385
Ming Bao China 11 366 0.9× 54 1.6× 18 0.8× 19 0.9× 10 1.1× 30 396
Kuntal Pal India 12 393 1.0× 52 1.6× 12 0.5× 23 1.0× 13 1.4× 27 415
Jan Wallbaum Germany 7 436 1.1× 23 0.7× 20 0.9× 13 0.6× 9 1.0× 9 446
Zhi‐Jie Niu China 14 333 0.8× 52 1.6× 39 1.8× 41 1.9× 7 0.8× 20 344
Ranjini Laskar Germany 7 301 0.7× 37 1.1× 30 1.4× 68 3.1× 9 1.0× 11 332

Countries citing papers authored by Rajendra K. Mallick

Since Specialization
Citations

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

Fields of papers citing papers by Rajendra K. Mallick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rajendra K. Mallick. 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 Rajendra K. Mallick. The network helps show where Rajendra K. Mallick may publish in the future.

Co-authorship network of co-authors of Rajendra K. Mallick

This figure shows the co-authorship network connecting the top 25 collaborators of Rajendra K. Mallick. A scholar is included among the top collaborators of Rajendra K. Mallick 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 Rajendra K. Mallick. Rajendra K. Mallick 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.
Dutta, Shubham, et al.. (2025). Synthetic Strategy for Unsymmetrical α-Fluoro-α′-aryl Ketones. Organic Letters. 27(3). 808–813.
2.
Zheng, Jia, et al.. (2024). Stereocontrolled Hydrogenation of Conjugated Enones to Alcohols via Dual Iridium‐Catalysis. Angewandte Chemie International Edition. 64(3). e202415171–e202415171. 4 indexed citations
3.
Mallick, Rajendra K., et al.. (2024). Benzo‐fused Nitrogen Heterocycles by Asymmetric Ring Expansion and Stereochemically Retentive Re‐contraction of Cyclic Ureas. Angewandte Chemie International Edition. 63(12). e202318417–e202318417. 6 indexed citations
4.
Saunthwal, Rakesh K., et al.. (2023). Enantioselective Intramolecular α‐Arylation of Benzylamine Derivatives: Synthesis of a Precursor to Levocetirizine. Angewandte Chemie International Edition. 62(14). e202216758–e202216758. 14 indexed citations
5.
Dutta, Shubham, Rajendra K. Mallick, & Akhila K. Sahoo. (2023). Regioselective Difunctionalization and Annulation of Ynamide. Angewandte Chemie. 135(30). 2 indexed citations
6.
Dutta, Shubham, Rajendra K. Mallick, & Akhila K. Sahoo. (2023). Regioselective Difunctionalization and Annulation of Ynamide. Angewandte Chemie International Edition. 62(30). e202300816–e202300816. 38 indexed citations
7.
Vanjari, Rajeshwer, B. Prabagar, Shengwen Yang, et al.. (2021). Yb(iii)-catalysed syn-thioallylation of ynamides. Chemical Communications. 57(61). 7521–7524. 18 indexed citations
8.
Mallick, Rajendra K., et al.. (2021). Keteniminium Induced Dienone‐Phenol Rearrangement and Intramolecular 6‐endo‐dig Cyclization Cascade of Yne‐Dienone. Helvetica Chimica Acta. 105(1). 3 indexed citations
9.
Mallick, Rajendra K., et al.. (2021). Lewis Acid-Driven Meyer–Schuster-Type Rearrangement of Yne-Dienone. The Journal of Organic Chemistry. 86(10). 7059–7068. 9 indexed citations
10.
Dutta, Shubham, Shengwen Yang, Rajeshwer Vanjari, et al.. (2020). Keteniminium‐Driven Umpolung Difunctionalization of Ynamides. Angewandte Chemie International Edition. 59(27). 10785–10790. 55 indexed citations
11.
Dutta, Shubham, Shengwen Yang, Rajeshwer Vanjari, et al.. (2020). Keteniminium‐Driven Umpolung Difunctionalization of Ynamides. Angewandte Chemie. 132(27). 10877–10882. 14 indexed citations
12.
Prabagar, B., et al.. (2019). Umpolung Reactivity of Ynamides: An Unconventional [1,3]‐Sulfonyl and [1,5]‐Sulfinyl Migration Cascade. Angewandte Chemie. 131(8). 2387–2392. 14 indexed citations
13.
Mallick, Rajendra K., Shubham Dutta, Rajeshwer Vanjari, Arnaud Voituriez, & Akhila K. Sahoo. (2019). Thioarylative Radical Cyclization of Yne-Dienone. The Journal of Organic Chemistry. 84(16). 10509–10517. 15 indexed citations
14.
Dutta, Shubham, et al.. (2018). Alkyne Versus Ynamide Reactivity: Regioselective Radical Cyclization of Yne‐Ynamides. Angewandte Chemie. 131(8). 2311–2316. 11 indexed citations
15.
Dutta, Shubham, et al.. (2018). Alkyne Versus Ynamide Reactivity: Regioselective Radical Cyclization of Yne‐Ynamides. Angewandte Chemie International Edition. 58(8). 2289–2294. 71 indexed citations
16.
Prabagar, B., et al.. (2018). Umpolung Reactivity of Ynamides: An Unconventional [1,3]‐Sulfonyl and [1,5]‐Sulfinyl Migration Cascade. Angewandte Chemie International Edition. 58(8). 2365–2370. 73 indexed citations
17.
Sahoo, Akhila K., Sanatan Nayak, B. Prabagar, Nayan Ghosh, & Rajendra K. Mallick. (2017). Ag(I)-Catalyzed Cycloisomerization and Cyclization of Ketene Aminals: Construction of Azepine and 1,2-Dihydropyridine Derivatives. Synthesis. 49(18). 4261–4271. 7 indexed citations
18.
Mallick, Rajendra K., B. Prabagar, & Akhila K. Sahoo. (2017). Regioselective Synthesis of 2,4,5-Trisubstituted Oxazoles and Ketene Aminals via Hydroamidation and Iodo-Imidation of Ynamides. The Journal of Organic Chemistry. 82(19). 10583–10594. 43 indexed citations
19.
Mallick, Rajendra K., S. Sethi, Madan Mohan Pradhan, et al.. (2016). Japanese Encephalitis Outbreak Among Children in Mayurbhanj, Odisha-India, 2015. Open Forum Infectious Diseases. 3(suppl_1). 1 indexed citations
20.
Prabagar, B., et al.. (2015). Triphenylphosphine promoted regio and stereoselective α-halogenation of ynamides. Organic Chemistry Frontiers. 3(1). 110–115. 27 indexed citations

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