Basudeb Achari

2.2k total citations
121 papers, 1.8k citations indexed

About

Basudeb Achari is a scholar working on Molecular Biology, Organic Chemistry and Plant Science. According to data from OpenAlex, Basudeb Achari has authored 121 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 61 papers in Organic Chemistry and 27 papers in Plant Science. Recurrent topics in Basudeb Achari's work include Carbohydrate Chemistry and Synthesis (25 papers), Natural product bioactivities and synthesis (23 papers) and Chemical Synthesis and Analysis (18 papers). Basudeb Achari is often cited by papers focused on Carbohydrate Chemistry and Synthesis (25 papers), Natural product bioactivities and synthesis (23 papers) and Chemical Synthesis and Analysis (18 papers). Basudeb Achari collaborates with scholars based in India, Japan and United Kingdom. Basudeb Achari's co-authors include Satyesh C. Pakrashi, Sukhendu Mandal, Pradeep K. Dutta, Niranjan P. Sahu, Ranjan Mukhopadhyay, Chinmay Chowdhury, Partha Chattopadhyay, Sukdeb Banerjee, Mainak Banerjee and Michael G. B. Drew and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and Antimicrobial Agents and Chemotherapy.

In The Last Decade

Basudeb Achari

117 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Basudeb Achari India 26 910 869 360 175 133 121 1.8k
Vibha Tandon India 28 832 0.9× 843 1.0× 298 0.8× 223 1.3× 205 1.5× 93 2.5k
Hideo Kamei Japan 27 1.0k 1.1× 750 0.9× 333 0.9× 133 0.8× 502 3.8× 87 2.5k
Mukund S. Chorghade India 20 550 0.6× 644 0.7× 153 0.4× 106 0.6× 130 1.0× 68 1.4k
Amooru G. Damu Taiwan 21 693 0.8× 297 0.3× 448 1.2× 221 1.3× 210 1.6× 30 1.4k
K.L. Dhar India 23 931 1.0× 803 0.9× 522 1.4× 191 1.1× 265 2.0× 86 2.1k
G. Rüċker Germany 20 680 0.7× 318 0.4× 496 1.4× 202 1.2× 230 1.7× 152 1.7k
Toshiyuki Akiyama Japan 25 1.1k 1.2× 324 0.4× 312 0.9× 365 2.1× 136 1.0× 79 1.9k
Keduo Qian United States 32 1.6k 1.7× 895 1.0× 310 0.9× 266 1.5× 298 2.2× 74 2.7k
Tetsuya Kajimoto Japan 31 2.0k 2.2× 1.9k 2.2× 326 0.9× 139 0.8× 300 2.3× 140 3.0k
Raymond W. Doskotch United States 22 729 0.8× 386 0.4× 411 1.1× 199 1.1× 237 1.8× 88 1.6k

Countries citing papers authored by Basudeb Achari

Since Specialization
Citations

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

Fields of papers citing papers by Basudeb Achari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Basudeb Achari

This figure shows the co-authorship network connecting the top 25 collaborators of Basudeb Achari. A scholar is included among the top collaborators of Basudeb Achari 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 Basudeb Achari. Basudeb Achari 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.
Mukhopadhyay, Chaitali, et al.. (2012). Design and synthesis of regioisomeric triazole based peptidomimetic macrocycles and their dipole moment controlled self-assembly. Chemical Communications. 48(98). 11975–11975. 20 indexed citations
2.
Bhadra, Kakali, et al.. (2011). Interaction of aristololactam-β-D-glucoside and daunomycin with poly(A): Spectroscopic and calorimetric studies. Biophysical Chemistry. 155(1). 10–19. 28 indexed citations
3.
Chowdhury, Chinmay, Anup Kumar Sasmal, & Basudeb Achari. (2010). An expedient and facile route for the general synthesis of 3-aryl substituted 1,2,3-triazolo[1,5-a][1,4]benzodiazepin-6-ones and 1,2,3-triazolo[1,5-a][1,5]benzodiazocin-7-ones. Organic & Biomolecular Chemistry. 8(21). 4971–4971. 16 indexed citations
4.
Chowdhury, Chinmay, et al.. (2009). Expedient and Rapid Synthesis of 1,2,3-Triazolo[5,1-c]morpholines through Palladium−Copper Catalysis. The Journal of Organic Chemistry. 74(9). 3612–3615. 31 indexed citations
6.
Drew, Michael G. B., et al.. (2007). First example of 5/6-O-linked pseudosaccharides: synthesis of bicyclic nucleosides containing azido or extended carbohydrate moiety. Carbohydrate Research. 342(17). 2511–2521. 11 indexed citations
7.
Dutta, Prasun, et al.. (2006). Isolation of pure compound R/J/3 from Pluchea indica (L.) Less. and its anti-amoebic activities against Entamoeba histolytica. Phytomedicine. 14(7-8). 534–537. 23 indexed citations
8.
Achari, Basudeb, et al.. (2005). Hopane-type saponins from Glinus lotoides Linn. Phytochemistry. 66(6). 621–626. 15 indexed citations
9.
Achari, Basudeb, et al.. (2005). Glucosides from Curculigo orchioides. Phytochemistry. 66(6). 659–663. 15 indexed citations
10.
Achari, Basudeb, et al.. (2005). Bicyclic nucleoside analogues from d-glucose: synthesis of chiral as well as racemic 1,4-dioxepane ring-fused derivatives. Carbohydrate Research. 340(6). 1081–1087. 10 indexed citations
11.
Chattopadhyay, Subhagata, et al.. (2005). Reaction of 2-[(E)-styryl]Quinazolin-4(3H)-one with Acetylenic Esters: Formation of Unexpected N-3 Alkenylation Products. Journal of Chemical Research. 2005(7). 429–431. 1 indexed citations
12.
Chowdhury, Chinmay, et al.. (2004). Perspectives on 1,4-Benzodioxins, 1,4-Benzoxazines and their 2,3-Dihydro Derivatives. Synlett. 2004(14). 2449–2467. 36 indexed citations
13.
Sahu, Niranjan P., Kazuo Koike, Sukdeb Banerjee, Basudeb Achari, & Tamotsu Nikaido. (2001). Triterpenoid saponins from Mollugo spergula. Phytochemistry. 58(8). 1177–1182. 25 indexed citations
14.
Roy, A. K., et al.. (1998). THE INFLUENCE OF ALPHA -AMIDO/THIOAMIDO FUNCTIONALITY IN ESTER REDUCTION WITH SODIUM BOROHYDRIDE. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 37(7). 644–650.
15.
Parveen, Mehtab, et al.. (1990). Triterpenoids from Garcinia mangostana.. Fitoterapia. 61(1). 86–87. 2 indexed citations
16.
Chakraborty, Saswati, et al.. (1989). Aristololactam-β-D-glucoside. Biochemical Pharmacology. 38(21). 3683–3687. 14 indexed citations
17.
Pakrashi, Satyesh C., et al.. (1989). Lipids and fatty acids of the horseshoe crabsTachypleus gigas andCarcinoscorpius rotundicauda. Lipids. 24(5). 443–447. 14 indexed citations
18.
Achari, Basudeb, et al.. (1986). A New Triterpene Ester, an Anthraquinone and Other Constituents of the FernLygodium flexuosum. Planta Medica. 52(4). 329–330. 11 indexed citations
19.
Dutta, Pradeep K., et al.. (1983). Studies on indian medicinal plants-part LXXV. Tetrahedron. 39(19). 3067–3072. 45 indexed citations
20.
Pakrashi, Satyesh C., et al.. (1983). A Phenanthroid Lactone, Steroid and Lignans from Aristolochia indica. Heterocycles. 20(5). 771–771. 13 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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