Ruja Shrestha

1.1k total citations
14 papers, 927 citations indexed

About

Ruja Shrestha is a scholar working on Organic Chemistry, Neurology and Molecular Biology. According to data from OpenAlex, Ruja Shrestha has authored 14 papers receiving a total of 927 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Organic Chemistry, 4 papers in Neurology and 2 papers in Molecular Biology. Recurrent topics in Ruja Shrestha's work include Catalytic C–H Functionalization Methods (8 papers), Catalytic Cross-Coupling Reactions (7 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Ruja Shrestha is often cited by papers focused on Catalytic C–H Functionalization Methods (8 papers), Catalytic Cross-Coupling Reactions (7 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Ruja Shrestha collaborates with scholars based in United States. Ruja Shrestha's co-authors include Daniel J. Weix, Daniel A. Everson, John F. Hartwig, Paramita Mukherjee, Yichen Tan, Jing Zhang, Pinjing Zhao, Shubhik DebBurman, Tulaza Vaidya and Nijee Sharma and has published in prestigious journals such as Journal of the American Chemical Society, SHILAP Revista de lepidopterología and Nature Chemistry.

In The Last Decade

Ruja Shrestha

12 papers receiving 915 citations

Peers

Ruja Shrestha
Vinayak Vishnu Pagar United States
Thomas N. Snaddon United States
Matthias Brewer United States
Guoyao Xia United States
Bryan J. Simmons United States
Zehong Wan United States
Ran Cheng China
Vinayak Vishnu Pagar United States
Ruja Shrestha
Citations per year, relative to Ruja Shrestha Ruja Shrestha (= 1×) peers Vinayak Vishnu Pagar

Countries citing papers authored by Ruja Shrestha

Since Specialization
Citations

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

Fields of papers citing papers by Ruja Shrestha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruja Shrestha

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

All Works

14 of 14 papers shown
1.
Shrestha, Ruja, et al.. (2017). Nickel-Catalyzed Reductive Conjugate Addition of Primary Alkyl Bromides to Enones To Form Silyl Enol Ethers. Organic Letters. 19(2). 340–343. 23 indexed citations
2.
Zhang, Jing, Ruja Shrestha, John F. Hartwig, & Pinjing Zhao. (2016). A decarboxylative approach for regioselective hydroarylation of alkynes. Nature Chemistry. 8(12). 1144–1151. 113 indexed citations
3.
Kelemen, Rachel E., et al.. (2015). Nickel-catalyzed reductive arylation of activated alkynes with aryl iodides. Tetrahedron Letters. 56(23). 3365–3367. 18 indexed citations
4.
Shrestha, Ruja, et al.. (2013). ChemInform Abstract: Nickel‐Catalyzed Reductive Conjugate Addition to Enones via Allylnickel Intermediates.. ChemInform. 44(33). 1 indexed citations
5.
Shrestha, Ruja, et al.. (2013). Sterically Controlled, Palladium-Catalyzed Intermolecular Amination of Arenes. Journal of the American Chemical Society. 135(23). 8480–8483. 159 indexed citations
6.
Shrestha, Ruja, et al.. (2012). Nickel-Catalyzed Reductive Conjugate Addition to Enones via Allylnickel Intermediates. Journal of the American Chemical Society. 135(2). 751–762. 93 indexed citations
7.
Shrestha, Ruja, William W. Brennessel, & Daniel J. Weix. (2011). [2,2′-Bis(diphenylphosphanyl)-1,1′-binaphthyl-κ2P,P′]chlorido(4-methylphenylsulfonyl-κS)palladium(II) dichloromethane trisolvate monohydrate. Acta Crystallographica Section E Structure Reports Online. 67(12). m1830–m1830. 1 indexed citations
8.
Shrestha, Ruja & Daniel J. Weix. (2011). Reductive Conjugate Addition of Haloalkanes to Enones To Form Silyl Enol Ethers. Organic Letters. 13(10). 2766–2769. 39 indexed citations
9.
Everson, Daniel A., Ruja Shrestha, & Daniel J. Weix. (2010). Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl Halides. Journal of the American Chemical Society. 132(10). 3636–3636. 10 indexed citations
10.
Everson, Daniel A., Ruja Shrestha, & Daniel J. Weix. (2010). Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl Halides. Journal of the American Chemical Society. 132(3). 920–921. 408 indexed citations
11.
Sharma, Nijee, et al.. (2006). α-Synuclein Budding Yeast Model: Toxicity Enhanced by Impaired Proteasome and Oxidative Stress. Journal of Molecular Neuroscience. 28(2). 161–178. 61 indexed citations
12.
Shrestha, Ruja, et al.. (2005). Newly Discovered a-Synuclein Familial Mutant E46K and Key Phosphorylation and Nitrosylation-Deficient Mutants are Toxic to Yeast. 1(1). 16.
13.
Paul, Arun George & Ruja Shrestha. (2005). Evaluation of Stp2p-dependent alpha-Synuclein Toxicity in Yeast: Role of GAPDH?. SHILAP Revista de lepidopterología. 1. 1 indexed citations
14.
Shrestha, Ruja, et al.. (2005). Vps28 Implicated in a-Synuclein Pathobiology: Building Support for Lysosome-Mediated Degradation.

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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