Y. Nanaji

468 total citations
13 papers, 356 citations indexed

About

Y. Nanaji is a scholar working on Organic Chemistry, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Y. Nanaji has authored 13 papers receiving a total of 356 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Organic Chemistry, 4 papers in Molecular Biology and 1 paper in Infectious Diseases. Recurrent topics in Y. Nanaji's work include Synthesis and Catalytic Reactions (7 papers), Catalytic C–H Functionalization Methods (6 papers) and Asymmetric Synthesis and Catalysis (3 papers). Y. Nanaji is often cited by papers focused on Synthesis and Catalytic Reactions (7 papers), Catalytic C–H Functionalization Methods (6 papers) and Asymmetric Synthesis and Catalysis (3 papers). Y. Nanaji collaborates with scholars based in India, United States and Germany. Y. Nanaji's co-authors include Manas K. Ghorai, Ashok Kumar Yadav, Nikhil Sharma, Gurpal Singh, Ravi Pratap Barnwal, Ashok Kumar Yadav, Dinesh Kumar, Aditya Bhattacharyya, Seema Kirar and Imtiyaz Ahmad Wani and has published in prestigious journals such as Inorganic Chemistry, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Y. Nanaji

12 papers receiving 351 citations

Peers

Y. Nanaji
Sachiko Yoshioka Japan
Lennart Lykke Denmark
Steven M. Wales Australia
Andreas Schumacher Switzerland
Clémence Liébert Germany
Richard E. Shute United Kingdom
Chongyang Wu China
Anna Brodzka Poland
Salvatore Petruso Italy
Anatol P. Spork Germany
Sachiko Yoshioka Japan
Y. Nanaji
Citations per year, relative to Y. Nanaji Y. Nanaji (= 1×) peers Sachiko Yoshioka

Countries citing papers authored by Y. Nanaji

Since Specialization
Citations

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

Fields of papers citing papers by Y. Nanaji

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Y. Nanaji

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

All Works

13 of 13 papers shown
1.
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Sharma, Nikhil, Y. Nanaji, Dinesh Kumar, et al.. (2023). Quorum sensing inhibitors as Therapeutics: Bacterial biofilm inhibition. Bioorganic Chemistry. 136. 106551–106551. 74 indexed citations
3.
Nanaji, Y., et al.. (2021). Cu-Catalyzed solvent-free, pot-economic synthesis of 1,3-dynes from 1,1-dibromoalkenes in the presence of DBU•H2O. ARKIVOC. 2021(8). 155–166. 1 indexed citations
4.
Nanaji, Y., Lavanya Dampanaboina, Venugopal Mendu, & Satyanarayana Battula. (2020). Synergistic factors ensue high expediency in the synthesis of menaquinone [K2] analogue MK-6: Application to access an efficient one-pot protocol to MK-9. Tetrahedron. 76(49). 131696–131696. 2 indexed citations
5.
Nanaji, Y., Seema Kirar, Sandip V. Pawar, & Ashok Kumar Yadav. (2020). A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines. RSC Advances. 10(13). 7628–7634. 23 indexed citations
6.
Biswas, Pronay Kumar, et al.. (2017). Influence of Rotator Design on the Speed of Self-Assembled Four-Component Nanorotors: Coordinative Versus Dispersive Interactions. Inorganic Chemistry. 56(11). 6662–6670. 25 indexed citations
7.
Wani, Imtiyaz Ahmad, et al.. (2017). A Synthetic Route to Chiral 1,4-Disubstituted Tetrahydro-β-Carbolines via Domino Ring-Opening Cyclization of Activated Aziridines with 2-Vinylindoles. The Journal of Organic Chemistry. 82(5). 2364–2374. 31 indexed citations
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Nanaji, Y., et al.. (2015). A Synthetic Route to 2-Alkyl Indoles via Thiophenol-Mediated Ring-Opening of N-Tosylaziridines Followed by Copper Powder-Mediated C–N Cyclization/Aromatization. The Journal of Organic Chemistry. 80(24). 12659–12667. 37 indexed citations
11.
Ghorai, Manas K. & Y. Nanaji. (2013). Synthetic Route to Chiral Indolines via Ring-Opening/C–N Cyclization of Activated 2-Haloarylaziridines. The Journal of Organic Chemistry. 78(8). 3867–3878. 34 indexed citations
12.
Ghorai, Manas K., et al.. (2013). Memory of Chirality (MOC) Concept in Imino-Aldol Reaction: Enantioselective Synthesis of α,β-Diamino Esters and Aziridines. The Journal of Organic Chemistry. 78(6). 2311–2326. 18 indexed citations
13.
Ghorai, Manas K., Y. Nanaji, & Ashok Kumar Yadav. (2011). Ring Opening/C–N Cyclization of Activated Aziridines with Carbon Nucleophiles: Highly Diastereo- and Enantioselective Synthesis of Tetrahydroquinolines. Organic Letters. 13(16). 4256–4259. 53 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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