Shinde Vidyacharan

611 total citations
18 papers, 529 citations indexed

About

Shinde Vidyacharan is a scholar working on Organic Chemistry, Biomedical Engineering and Molecular Biology. According to data from OpenAlex, Shinde Vidyacharan has authored 18 papers receiving a total of 529 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 7 papers in Biomedical Engineering and 5 papers in Molecular Biology. Recurrent topics in Shinde Vidyacharan's work include Multicomponent Synthesis of Heterocycles (8 papers), Innovative Microfluidic and Catalytic Techniques Innovation (7 papers) and Synthesis and Biological Evaluation (5 papers). Shinde Vidyacharan is often cited by papers focused on Multicomponent Synthesis of Heterocycles (8 papers), Innovative Microfluidic and Catalytic Techniques Innovation (7 papers) and Synthesis and Biological Evaluation (5 papers). Shinde Vidyacharan collaborates with scholars based in India, South Korea and Singapore. Shinde Vidyacharan's co-authors include Duddu S. Sharada, Anand H. Shinde, A. Sagar, Dong‐Pyo Kim, Bishnupada Satpathi, Seungwook Jang, R. Reshma, Niraj Kumar Vishwakarma, Dharmarajan Sriram and Chandan Adhikari and has published in prestigious journals such as Green Chemistry, The Journal of Organic Chemistry and Lab on a Chip.

In The Last Decade

Shinde Vidyacharan

18 papers receiving 526 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shinde Vidyacharan India 15 458 112 80 40 23 18 529
Dmitry B. Ushakov Germany 8 271 0.6× 73 0.7× 103 1.3× 51 1.3× 52 2.3× 9 371
Xiao Yin Mak United States 7 365 0.8× 73 0.7× 143 1.8× 71 1.8× 25 1.1× 10 453
Sharada Prasanna Swain India 12 294 0.6× 65 0.6× 44 0.6× 50 1.3× 33 1.4× 31 387
Luis Bering Germany 12 420 0.9× 162 1.4× 41 0.5× 67 1.7× 22 1.0× 14 514
Thiwanka B. Samarakoon United States 13 418 0.9× 133 1.2× 50 0.6× 34 0.8× 12 0.5× 19 460
Isravel Muthukrishnan India 8 487 1.1× 92 0.8× 38 0.5× 139 3.5× 19 0.8× 10 529
Julia C. Reisenbauer Switzerland 9 405 0.9× 122 1.1× 21 0.3× 72 1.8× 30 1.3× 11 504
Adam T. Gillmore United Kingdom 9 399 0.9× 92 0.8× 35 0.4× 58 1.4× 28 1.2× 13 483
Michael C. Weismiller United States 9 319 0.7× 65 0.6× 30 0.4× 59 1.5× 29 1.3× 12 418
Dumei Ma China 12 267 0.6× 63 0.6× 52 0.7× 85 2.1× 12 0.5× 25 371

Countries citing papers authored by Shinde Vidyacharan

Since Specialization
Citations

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

Fields of papers citing papers by Shinde Vidyacharan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shinde Vidyacharan

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

All Works

18 of 18 papers shown
1.
Ahn, Gwang‐Noh, et al.. (2021). Flow parallel synthesizer for multiplex synthesis of aryl diazonium libraries via efficient parameter screening. Communications Chemistry. 4(1). 53–53. 20 indexed citations
2.
Vidyacharan, Shinde, et al.. (2020). Ultrafast synthesis of 2-(benzhydrylthio)benzo[d]oxazole, an antimalarial drug, via an unstable lithium thiolate intermediate in a capillary microreactor. Reaction Chemistry & Engineering. 5(5). 849–852. 6 indexed citations
3.
Vidyacharan, Shinde, et al.. (2020). Compact reaction-module on a pad for scalable flow-production of organophosphates as drug scaffolds. Lab on a Chip. 20(5). 973–978. 16 indexed citations
4.
Vidyacharan, Shinde, et al.. (2019). Continuous‐Flow Visible Light Organophotocatalysis for Direct Arylation of 2H‐Indazoles: Fast Access to Drug Molecules. ChemSusChem. 12(12). 2581–2586. 46 indexed citations
5.
Jang, Seungwook, et al.. (2019). Photocatalysis in a multi-capillary assembly microreactor: toward up-scaling the synthesis of 2H-indazoles as drug scaffolds. Reaction Chemistry & Engineering. 4(8). 1466–1471. 20 indexed citations
6.
Vidyacharan, Shinde, et al.. (2019). Fast‐Synthesis of α‐Phosphonyloxy Ketones as Drug Scaffolds in a Capillary Microreactor. European Journal of Organic Chemistry. 2019(47). 7730–7734. 2 indexed citations
7.
Vishwakarma, Niraj Kumar, et al.. (2018). Towards Versatile Continuous‐Flow Chemistry and Process Technology Via New Conceptual Microreactor Systems. Bulletin of the Korean Chemical Society. 39(6). 757–772. 31 indexed citations
8.
Vidyacharan, Shinde, Chandan Adhikari, Vagolu Siva Krishna, et al.. (2017). A robust synthesis of functionalized 2H-indazoles via solid state melt reaction (SSMR) and their anti-tubercular activity. Bioorganic & Medicinal Chemistry Letters. 27(7). 1593–1597. 33 indexed citations
9.
Vidyacharan, Shinde, et al.. (2017). Metal‐Free Regioselective Dual C‐H Functionalization in a Cascade Fashion: Access to Isocryptolepine Alkaloid Analogues. ChemistrySelect. 2(12). 3511–3515. 7 indexed citations
10.
Sharada, Duddu S., et al.. (2016). Scaffold Diversity through a Branching Double-Annulation Cascade Strategy: Iminium-Induced One-Pot Synthesis of Diverse Fused Tetrahydroisoquinoline Scaffolds. The Journal of Organic Chemistry. 81(15). 6463–6471. 17 indexed citations
11.
Vidyacharan, Shinde, et al.. (2016). C(sp2)–H Functionalization of 2H-Indazoles at C3-Position via Palladium(II)-Catalyzed Isocyanide Insertion Strategy Leading to Diverse Heterocycles. The Journal of Organic Chemistry. 81(7). 2837–2848. 69 indexed citations
12.
Shinde, Anand H., Shinde Vidyacharan, & Duddu S. Sharada. (2016). BF3·OEt2 mediated metal-free one-pot sequential multiple annulation cascade (SMAC) synthesis of complex and diverse tetrahydroisoquinoline fused hybrid molecules. Organic & Biomolecular Chemistry. 14(12). 3207–3211. 26 indexed citations
13.
Vidyacharan, Shinde, A. Sagar, & Duddu S. Sharada. (2015). A new route for the synthesis of highly substituted 4-aminoquinoline drug like molecules via aza hetero–Diels–Alder reaction. Organic & Biomolecular Chemistry. 13(28). 7614–7618. 24 indexed citations
14.
Sagar, A., Shinde Vidyacharan, & Duddu S. Sharada. (2014). I2-promoted cross-dehydrogenative coupling of α-carbonyl aldehydes with alcohols for the synthesis of α-ketoesters. RSC Advances. 4(70). 37047–37047. 37 indexed citations
15.
Vidyacharan, Shinde, et al.. (2014). One-Pot Palladium-Catalyzed Ligand- and Metal-Oxidant-Free Aerobic Oxidative Isocyanide Insertion Leading to 2-Amino-substituted-4(3H)-quinazolinones. Synthetic Communications. 45(7). 898–907. 19 indexed citations
17.
Shinde, Anand H., Shinde Vidyacharan, & Duddu S. Sharada. (2014). Microwave-assisted facile synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular azomethine imine 1,3-dipolar cycloaddition. Tetrahedron Letters. 55(19). 3064–3069. 23 indexed citations
18.
Vidyacharan, Shinde, Anand H. Shinde, Bishnupada Satpathi, & Duddu S. Sharada. (2013). A facile protocol for the synthesis of 3-aminoimidazo-fused heterocycles via the Groebke–Blackburn–Bienayme reaction under catalyst-free and solvent-free conditions. Green Chemistry. 16(3). 1168–1168. 92 indexed citations

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