Manohar Saindane

2.8k total citations · 1 hit paper
40 papers, 1.1k citations indexed

About

Manohar Saindane is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Manohar Saindane has authored 40 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Organic Chemistry, 11 papers in Molecular Biology and 10 papers in Toxicology. Recurrent topics in Manohar Saindane's work include Organoselenium and organotellurium chemistry (8 papers), Asymmetric Synthesis and Catalysis (5 papers) and Organic Chemistry Cycloaddition Reactions (5 papers). Manohar Saindane is often cited by papers focused on Organoselenium and organotellurium chemistry (8 papers), Asymmetric Synthesis and Catalysis (5 papers) and Organic Chemistry Cycloaddition Reactions (5 papers). Manohar Saindane collaborates with scholars based in United States, India and Germany. Manohar Saindane's co-authors include Dennis C. Liotta, Frederick E. Ziegler, Michael G. Natchus, Burton H. Jaynes, George Zima, George R. Painter, Alexander A. Kolykhalov, Liladhar Waykole, Gregory R. Bluemling and Mark A. Lockwood and has published in prestigious journals such as Journal of the American Chemical Society, Nature Communications and Journal of Virology.

In The Last Decade

Manohar Saindane

40 papers receiving 1.0k citations

Hit Papers

Small-Molecule Antiviral β- d - N 4 -Hydroxycytidine Inhi... 2019 2026 2021 2023 2019 50 100 150 200 250

Peers

Manohar Saindane
Yat Sun Or United States
Lucia Gerena United States
Gregory S. Bisacchi United States
Paul A. Stocks United Kingdom
Manohar Saindane
Citations per year, relative to Manohar Saindane Manohar Saindane (= 1×) peers Francisca Lopes

Countries citing papers authored by Manohar Saindane

Since Specialization
Citations

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

Fields of papers citing papers by Manohar Saindane

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manohar Saindane

This figure shows the co-authorship network connecting the top 25 collaborators of Manohar Saindane. A scholar is included among the top collaborators of Manohar Saindane 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 Manohar Saindane. Manohar Saindane 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.
Westover, Jonna B., Cigdem Alkan, Arnaud J. Van Wettere, et al.. (2024). Modeling Heartland virus disease in mice and therapeutic intervention with 4′-fluorouridine. Journal of Virology. 98(4). e0013224–e0013224. 8 indexed citations
2.
Lieber, Carolin M., Megha Aggarwal, Jeong-Joong Yoon, et al.. (2023). 4’-Fluorouridine mitigates lethal infection with pandemic human and highly pathogenic avian influenza viruses. PLoS Pathogens. 19(4). e1011342–e1011342. 20 indexed citations
3.
Lieber, Carolin M., Robert M. Cox, Julien Sourimant, et al.. (2022). SARS-CoV-2 VOC type and biological sex affect molnupiravir efficacy in severe COVID-19 dwarf hamster model. Nature Communications. 13(1). 4416–4416. 33 indexed citations
4.
Agostini, Maria L., Andrea J. Pruijssers, James D. Chappell, et al.. (2019). Small-Molecule Antiviral β- d - N 4 -Hydroxycytidine Inhibits a Proofreading-Intact Coronavirus with a High Genetic Barrier to Resistance. Journal of Virology. 93(24). 255 indexed citations breakdown →
5.
Sayeed, Iqbal, Bushra Wali, David B. Guthrie, et al.. (2018). Development of a novel progesterone analog in the treatment of traumatic brain injury. Neuropharmacology. 145(Pt B). 292–298. 11 indexed citations
6.
Moore, Terry W., Dan Yan, John M. Ndungu, et al.. (2013). Asymmetric synthesis of host-directed inhibitors of myxoviruses. Beilstein Journal of Organic Chemistry. 9. 197–203. 12 indexed citations
7.
Zhao, Huanyu, Brooke M. Katzman, Ana A. Alcaraz, et al.. (2013). Discovery of Tetrahydroisoquinoline-Based CXCR4 Antagonists. ACS Medicinal Chemistry Letters. 4(11). 1025–1030. 55 indexed citations
8.
Qian, Xinhua, et al.. (2002). A Stereoselective Synthesis of BMS-262084, an Azetidinone-Based Tryptase Inhibitor. The Journal of Organic Chemistry. 67(11). 3595–3600. 22 indexed citations
9.
Reuman, Michael, Sol J. Daum, Baldev Singh, et al.. (1995). Synthesis and Antibacterial Activity of Some Novel 1-Substituted 1,4-Dihydro-4-oxo-7-pyridinyl-3-quinolinecarboxylic Acids. Potent Antistaphylococcal Agents. Journal of Medicinal Chemistry. 38(14). 2531–2540. 21 indexed citations
10.
Desai, Ranjit C., et al.. (1994). An Efficient Large Scale Synthesis of 4-Isopropyl- and 4-Isopropyl-6-methoxybenzisothiazolones. The Journal of Organic Chemistry. 59(23). 7161–7163. 11 indexed citations
11.
Swiss, Kevin A., et al.. (1990). Reactions involving selenium metal as an electrophile: Scope and limitations of the enolate‐selenolate transformation. Heteroatom Chemistry. 1(2). 141–149. 1 indexed citations
12.
Liotta, Dennis C., et al.. (1988). Trajectories of proton transfer reactions. Experimental determination of the magnitude of primary deuterium isotope effects for proton-transfers occuring at acute angles. Journal of the American Chemical Society. 110(8). 2667–2668. 11 indexed citations
13.
Liotta, Dennis C., et al.. (1986). Rearrangement of α-Phenylselenenylketones. Synthetic Communications. 16(12). 1461–1468. 5 indexed citations
14.
Liotta, Dennis C., et al.. (1985). Synthetic applications of 2-phenylselenenylenones—III. Tetrahedron. 41(21). 4881–4889. 15 indexed citations
15.
Liotta, Dennis C., et al.. (1985). Acetylide additions to enediones. Regioselectivity based on stereoelectronic control. The Journal of Organic Chemistry. 50(17). 3241–3243. 20 indexed citations
16.
Liotta, Dennis C., et al.. (1981). ChemInform Abstract: SELECTIVE REACTIONS OF CARBANIONS WITH P‐QUINONES. THE AGGREGATE MODEL. Chemischer Informationsdienst. 12(51). 1 indexed citations
17.
Liotta, Dennis C., et al.. (1981). Reactions involving selenium metal as an electrophile. 2. A general procedure for the preparation of unsaturated β-dicarbonyl compounds. Tetrahedron Letters. 22(32). 3043–3046. 10 indexed citations
18.
Liotta, Dennis C., et al.. (1981). Selective reactions of carbanions with p-quinones. The aggregate model. The Journal of Organic Chemistry. 46(16). 3369–3370. 14 indexed citations
19.
Liotta, Dennis C., et al.. (1980). Reactions involving selenium metal as an electrophile. The enolate - selenolate transformation. Tetrahedron Letters. 21(38). 3643–3646. 15 indexed citations
20.
Saindane, Manohar, et al.. (1975). Flavanoids—III. Tetrahedron. 31(8). 1011–1013. 1 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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