Sajal Das

1.3k total citations
57 papers, 1.0k citations indexed

About

Sajal Das is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Sajal Das has authored 57 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Organic Chemistry, 8 papers in Molecular Biology and 7 papers in Inorganic Chemistry. Recurrent topics in Sajal Das's work include Catalytic C–H Functionalization Methods (23 papers), Catalytic Cross-Coupling Reactions (16 papers) and Sulfur-Based Synthesis Techniques (14 papers). Sajal Das is often cited by papers focused on Catalytic C–H Functionalization Methods (23 papers), Catalytic Cross-Coupling Reactions (16 papers) and Sulfur-Based Synthesis Techniques (14 papers). Sajal Das collaborates with scholars based in India, United States and Sweden. Sajal Das's co-authors include Prasanjit Ghosh, Bhaskar Ganguly, Basudeb Basu, Pralay Das, Sumanta Gupta, Fredrik Almqvist, Bablee Mandal, Seema Dwivedi, Hans Andersson and Roger Olsson and has published in prestigious journals such as Chemical Communications, Journal of Colloid and Interface Science and The Journal of Organic Chemistry.

In The Last Decade

Sajal Das

56 papers receiving 995 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sajal Das India 20 936 135 107 62 60 57 1.0k
Vishnu P. Srivastava India 24 1.2k 1.3× 200 1.5× 97 0.9× 38 0.6× 51 0.8× 50 1.3k
Cécile Savarin United States 14 929 1.0× 133 1.0× 95 0.9× 106 1.7× 34 0.6× 17 1.0k
M. N. V. Sastry Taiwan 12 1.1k 1.2× 111 0.8× 110 1.0× 72 1.2× 26 0.4× 18 1.1k
K. Ramesh India 23 1.2k 1.3× 214 1.6× 60 0.6× 89 1.4× 26 0.4× 59 1.3k
Kalicharan Chattopadhyay India 14 733 0.8× 80 0.6× 114 1.1× 131 2.1× 21 0.3× 23 795
Weisi Guo China 23 1.3k 1.4× 61 0.5× 121 1.1× 66 1.1× 150 2.5× 53 1.5k
Fu‐Yu Tsai Taiwan 21 1.4k 1.5× 102 0.8× 214 2.0× 159 2.6× 29 0.5× 58 1.5k
Sukalyan Bhadra India 21 1.5k 1.6× 188 1.4× 249 2.3× 108 1.7× 38 0.6× 49 1.5k
N. Srilakshmi Krishnaveni India 16 899 1.0× 231 1.7× 165 1.5× 74 1.2× 21 0.3× 40 992
Zhen-Chu Chen China 18 1.2k 1.3× 111 0.8× 118 1.1× 53 0.9× 23 0.4× 99 1.3k

Countries citing papers authored by Sajal Das

Since Specialization
Citations

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

Fields of papers citing papers by Sajal Das

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sajal Das

This figure shows the co-authorship network connecting the top 25 collaborators of Sajal Das. A scholar is included among the top collaborators of Sajal Das 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 Sajal Das. Sajal Das 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.
Mandal, Samir, Prasanjit Ghosh, & Sajal Das. (2025). Synthesis of dihydropyrimidinones via urea-based multicomponent reactions. Organic & Biomolecular Chemistry. 23(21). 5064–5080. 2 indexed citations
2.
Ghosh, Prasanjit, et al.. (2024). Copper( ii )-catalyzed, site-selective C(sp) 2 –H amination using 8-aminoimidazo[1,2- a ]pyridine (8-AIP) as a directing group. Organic & Biomolecular Chemistry. 22(32). 6617–6630. 3 indexed citations
3.
4.
Ghosh, Prasanjit, et al.. (2023). Tert‐Butylnitrite Mediated Regioselective C(sp2)−3 Nitration of Substituted 4‐Quinolones and Its Late‐stage Manipulations. Asian Journal of Organic Chemistry. 12(9). 2 indexed citations
5.
Sinha, Archana, Anupam Nath Jha, Debasis Manna, et al.. (2023). A small molecule potent IRAK4 inhibitor abrogates lipopolysaccharide-induced macrophage inflammation in-vitro and in-vivo. European Journal of Pharmacology. 944. 175593–175593. 8 indexed citations
6.
Ghosh, Prasanjit, et al.. (2023). Copper(II)-Mediated, Site-Selective C(sp2)–H Sulfonamidation of 1-Naphthylamines. The Journal of Organic Chemistry. 88(24). 16985–16996. 5 indexed citations
7.
Ghosh, Prasanjit & Sajal Das. (2021). The C–H functionalization of N-alkoxycarbamoyl indoles by transition metal catalysis. Organic & Biomolecular Chemistry. 19(37). 7949–7969. 12 indexed citations
8.
Ghosh, Prasanjit, et al.. (2021). Metal free C-3 chalcogenation (sulfenylation and selenylation) of 4H-pyrido[1,2-a]pyrimidin-4-ones. RSC Advances. 11(17). 10258–10263. 20 indexed citations
9.
Ghosh, Prasanjit, et al.. (2019). Creation of thio and selenocyanate derivatives of 4-quinolone via regioselective C–H bond functionalization under ambient conditions. New Journal of Chemistry. 43(27). 10959–10964. 23 indexed citations
10.
Ghosh, Prasanjit, et al.. (2018). Green procedure for highly efficient, rapid synthesis of imidazo[1,2-a]pyridine and its late stage functionalization. Synthetic Communications. 48(9). 1076–1084. 29 indexed citations
11.
Ghosh, Prasanjit, et al.. (2018). Generation of ArS- and ArSe-Substituted 4-Quinolone Derivatives Using Sodium Iodide As an Inducer. The Journal of Organic Chemistry. 83(20). 12411–12419. 39 indexed citations
12.
Kundu, Kaushik, et al.. (2014). Formation, thermodynamic properties, microstructures and antimicrobial activity of mixed cationic/non-ionic surfactant microemulsions with isopropyl myristate as oil. Journal of Colloid and Interface Science. 430. 129–139. 23 indexed citations
13.
Dwivedi, Seema, et al.. (2014). A green protocol for the Pd catalyzed ligand free homocoupling reaction of arylboronic acids under ambient conditions. RSC Advances. 4(77). 41045–41050. 19 indexed citations
14.
Andersson, Hans, et al.. (2010). Efficient, mild and completely regioselective synthesis of substituted pyridines. Chemical Communications. 46(19). 3384–3384. 49 indexed citations
15.
Basu, Basudeb, et al.. (2009). Catechol violet as new, efficient, and versatile ligand for Cu(I)-catalyzed C–S coupling reactions. Tetrahedron Letters. 50(39). 5523–5528. 35 indexed citations
16.
Basu, Basudeb, Sajal Das, & Bablee Mandal. (2008). Role of copper in catalyzing aryl and heteroaryl-nitrogen (or -oxygen) bond formation under ligand-free and solvent-free conditions. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 47(11). 1701–1706. 2 indexed citations
17.
Basu, Basudeb, Bablee Mandal, Sajal Das, Pralay Das, & Ashis Kumar Nanda. (2008). Chemoselective reduction of aldehydes by ruthenium trichloride and resin-bound formates. Beilstein Journal of Organic Chemistry. 4. 53–53. 11 indexed citations
18.
Basu, Basudeb, Pralay Das, & Sajal Das. (2005). Transfer hydrogenation using recyclable polymer-supported formate (PSF): Efficient and chemoselective reduction of nitroarenes. Molecular Diversity. 9(4). 259–262. 12 indexed citations
19.
Basu, Basudeb, et al.. (2005). Palladium-Catalyzed Selective Amination of Haloaromatics on KF-Alumina Surface. Synlett. 2005(8). 1275–1278. 8 indexed citations
20.
Basu, Basudeb, et al.. (2005). Co-immobilized formate anion and palladium on a polymer surface: a novel heterogeneous combination for transfer hydrogenation. Tetrahedron Letters. 46(49). 8591–8593. 16 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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