Arvind Jaganathan

1.1k total citations
17 papers, 962 citations indexed

About

Arvind Jaganathan is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmacology. According to data from OpenAlex, Arvind Jaganathan has authored 17 papers receiving a total of 962 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 13 papers in Inorganic Chemistry and 2 papers in Pharmacology. Recurrent topics in Arvind Jaganathan's work include Vanadium and Halogenation Chemistry (13 papers), Chemical Synthesis and Reactions (7 papers) and Catalytic C–H Functionalization Methods (6 papers). Arvind Jaganathan is often cited by papers focused on Vanadium and Halogenation Chemistry (13 papers), Chemical Synthesis and Reactions (7 papers) and Catalytic C–H Functionalization Methods (6 papers). Arvind Jaganathan collaborates with scholars based in United States. Arvind Jaganathan's co-authors include Babak Borhan, Daniel C. Whitehead, Richard J. Staples, Roozbeh Yousefi, Atefeh Garzan, James E. Jackson, Kumar Dilip Ashtekar, Daniel Holmes, Yi Yi and Paméla Pollet and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

Arvind Jaganathan

16 papers receiving 961 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arvind Jaganathan United States 13 891 681 109 76 43 17 962
Roozbeh Yousefi United States 8 611 0.7× 530 0.8× 69 0.6× 34 0.4× 22 0.5× 10 706
William Kuester United States 5 593 0.7× 455 0.7× 65 0.6× 80 1.1× 23 0.5× 5 656
Hang‐Fei Tu China 14 1.4k 1.5× 484 0.7× 66 0.6× 85 1.1× 144 3.3× 18 1.4k
Won‐jin Chung South Korea 16 808 0.9× 283 0.4× 64 0.6× 97 1.3× 97 2.3× 38 931
Ruben M. Martinez United States 3 1.0k 1.2× 327 0.5× 58 0.5× 99 1.3× 148 3.4× 4 1.2k
Sandy Ma United States 13 1.4k 1.6× 475 0.7× 63 0.6× 228 3.0× 128 3.0× 14 1.6k
Ren‐Xiao Liang China 23 1.7k 1.9× 347 0.5× 29 0.3× 94 1.2× 70 1.6× 60 1.8k
Souvik Rakshit Germany 12 2.8k 3.1× 517 0.8× 44 0.4× 79 1.0× 101 2.3× 15 2.8k
Subhajit Bhunia India 17 1.4k 1.6× 216 0.3× 76 0.7× 63 0.8× 120 2.8× 19 1.5k
Xiao‐Wei Liang China 14 766 0.9× 178 0.3× 69 0.6× 63 0.8× 94 2.2× 19 794

Countries citing papers authored by Arvind Jaganathan

Since Specialization
Citations

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

Fields of papers citing papers by Arvind Jaganathan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arvind Jaganathan

This figure shows the co-authorship network connecting the top 25 collaborators of Arvind Jaganathan. A scholar is included among the top collaborators of Arvind Jaganathan 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 Arvind Jaganathan. Arvind Jaganathan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Jaganathan, Arvind, et al.. (2024). Synthesis of N-Bromo and N-Iodo Imides: A Rapid Redox-Neutral and Bench Stable Process. Organic Process Research & Development. 28(11). 3959–3962.
2.
Sarkar, Aritra, et al.. (2023). Structure–Enantioselectivity Relationship (SER) Study of Cinchona Alkaloid Chlorocyclization Catalysts. The Journal of Organic Chemistry. 89(17). 11921–11929. 3 indexed citations
3.
Yousefi, Roozbeh, et al.. (2018). Absolute and relative facial selectivities in organocatalytic asymmetric chlorocyclization reactions. Chemical Science. 9(11). 2898–2908. 22 indexed citations
4.
Li, Zhao, Jason S. Fisk, Arvind Jaganathan, et al.. (2017). Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base. New Journal of Chemistry. 41(24). 15420–15432. 11 indexed citations
5.
Jaganathan, Arvind, et al.. (2017). Highly Regio- and Enantioselective Vicinal Dihalogenation of Allyl Amides. Journal of the American Chemical Society. 139(6). 2132–2135. 51 indexed citations
6.
Li, Zhao, Jason S. Fisk, Arvind Jaganathan, et al.. (2016). Aqueous Suzuki Coupling Reactions of Basic Nitrogen-Containing Substrates in the Absence of Added Base and Ligand: Observation of High Yields under Acidic Conditions. The Journal of Organic Chemistry. 81(18). 8520–8529. 16 indexed citations
7.
Li, Zhao, et al.. (2016). Palladium-Catalyzed Suzuki Reactions in Water with No Added Ligand: Effects of Reaction Scale, Temperature, pH of Aqueous Phase, and Substrate Structure. Organic Process Research & Development. 20(8). 1489–1499. 39 indexed citations
8.
Jaganathan, Arvind, et al.. (2015). Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides. Angewandte Chemie International Edition. 54(33). 9517–9522. 53 indexed citations
9.
Jaganathan, Arvind, et al.. (2015). Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides. Angewandte Chemie. 127(33). 9653–9658. 12 indexed citations
10.
Zhang, Chunming, et al.. (2015). Synthetic Optimization and Scale-Up of Imino–Amido Hafnium and Zirconium Olefin Polymerization Catalysts. Organic Process Research & Development. 19(10). 1383–1391. 14 indexed citations
11.
Ashtekar, Kumar Dilip, et al.. (2014). A New Tool To Guide Halofunctionalization Reactions: The Halenium Affinity (HalA) Scale. Journal of the American Chemical Society. 136(38). 13355–13362. 73 indexed citations
12.
Jaganathan, Arvind & Babak Borhan. (2014). Chlorosulfonamide Salts Are Superior Electrophilic Chlorine Precursors for the Organocatalytic Asymmetric Chlorocyclization of Unsaturated Amides. Organic Letters. 16(14). 3616–3619. 41 indexed citations
13.
Garzan, Atefeh, Arvind Jaganathan, Roozbeh Yousefi, et al.. (2013). Solvent‐Dependent Enantiodivergence in the Chlorocyclization of Unsaturated Carbamates. Chemistry - A European Journal. 19(27). 9015–9021. 63 indexed citations
14.
Jaganathan, Arvind, Richard J. Staples, & Babak Borhan. (2013). Kinetic Resolution of Unsaturated Amides in a Chlorocyclization Reaction: Concomitant Enantiomer Differentiation and Face Selective Alkene Chlorination by a Single Catalyst. Journal of the American Chemical Society. 135(39). 14806–14813. 65 indexed citations
15.
Jaganathan, Arvind, Atefeh Garzan, Daniel C. Whitehead, Richard J. Staples, & Babak Borhan. (2011). A Catalytic Asymmetric Chlorocyclization of Unsaturated Amides. Angewandte Chemie International Edition. 50(11). 2593–2596. 169 indexed citations
16.
Jaganathan, Arvind, Atefeh Garzan, Daniel C. Whitehead, Richard J. Staples, & Babak Borhan. (2011). A Catalytic Asymmetric Chlorocyclization of Unsaturated Amides. Angewandte Chemie. 123(11). 2641–2644. 49 indexed citations
17.
Whitehead, Daniel C., Roozbeh Yousefi, Arvind Jaganathan, & Babak Borhan. (2010). An Organocatalytic Asymmetric Chlorolactonization. Journal of the American Chemical Society. 132(10). 3298–3300. 281 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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