Govindaswamy Manickam

436 total citations
21 papers, 350 citations indexed

About

Govindaswamy Manickam is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Govindaswamy Manickam has authored 21 papers receiving a total of 350 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Organic Chemistry, 6 papers in Molecular Biology and 6 papers in Inorganic Chemistry. Recurrent topics in Govindaswamy Manickam's work include Asymmetric Synthesis and Catalysis (7 papers), Chemical Synthesis and Analysis (6 papers) and Catalytic Cross-Coupling Reactions (5 papers). Govindaswamy Manickam is often cited by papers focused on Asymmetric Synthesis and Catalysis (7 papers), Chemical Synthesis and Analysis (6 papers) and Catalytic Cross-Coupling Reactions (5 papers). Govindaswamy Manickam collaborates with scholars based in India, Germany and Switzerland. Govindaswamy Manickam's co-authors include G. Sundararajan, Shanmugam Muthusubramanian, Yong Li, R. Senthil Kumaran, A. Dieter Schlüter, Asit R. Sarkar, Jayadevan Jayashankaran, Motomu Kanai, Harald Gröger and Masakatsu Shibasaki and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and RSC Advances.

In The Last Decade

Govindaswamy Manickam

19 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Govindaswamy Manickam India 12 323 67 66 21 15 21 350
P. Sreedhar India 8 344 1.1× 59 0.9× 54 0.8× 26 1.2× 11 0.7× 12 369
Jan Tois Finland 12 357 1.1× 97 1.4× 85 1.3× 20 1.0× 19 1.3× 26 405
Michael H. Wu United States 6 250 0.8× 48 0.7× 68 1.0× 26 1.2× 15 1.0× 7 282
Takayuki Tsuritani Japan 15 505 1.6× 109 1.6× 52 0.8× 16 0.8× 15 1.0× 22 531
Enrique Aller Spain 12 378 1.2× 93 1.4× 54 0.8× 17 0.8× 28 1.9× 20 420
Natsuki Nakamichi Japan 6 480 1.5× 65 1.0× 58 0.9× 50 2.4× 10 0.7× 8 518
Christoph Weckbecker Germany 8 345 1.1× 77 1.1× 116 1.8× 32 1.5× 22 1.5× 8 405
Esa T. T. Kumpulainen Finland 8 312 1.0× 76 1.1× 103 1.6× 50 2.4× 12 0.8× 12 361
Kazuhiko Kato Japan 6 507 1.6× 68 1.0× 151 2.3× 13 0.6× 19 1.3× 10 526
Zhen‐Kang Wen China 11 383 1.2× 29 0.4× 78 1.2× 24 1.1× 17 1.1× 20 420

Countries citing papers authored by Govindaswamy Manickam

Since Specialization
Citations

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

Fields of papers citing papers by Govindaswamy Manickam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Govindaswamy Manickam

This figure shows the co-authorship network connecting the top 25 collaborators of Govindaswamy Manickam. A scholar is included among the top collaborators of Govindaswamy Manickam 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 Govindaswamy Manickam. Govindaswamy Manickam 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.
Srinivasan, R., et al.. (2015). A Convenient One‐Pot Synthesis of Triazolopyridine and Related Heterocycle Fused‐Triazole Analogs Through Copper Catalyzed Oxidative Cyclization Strategy. Journal of Heterocyclic Chemistry. 53(2). 606–614. 12 indexed citations
2.
3.
Muthusubramanian, Shanmugam, et al.. (2014). C2‐Arylation of Substituted Pyridine N‐oxides with Heteroaryl Carboxylic Acids by Palladium‐Catalyzed Decarboxylative Coupling. Asian Journal of Organic Chemistry. 3(5). 604–608. 24 indexed citations
4.
Muthusubramanian, Shanmugam, et al.. (2013). ChemInform Abstract: Acid‐Controlled Generation of Indans and Oxazolines from β‐Hydroxyarylethanamide.. ChemInform. 44(33). 2 indexed citations
5.
6.
Ilangovan, Andivelu, et al.. (2013). A convenient approach for the deprotection and scavenging of the PMB group using POCl3. RSC Advances. 3(34). 14814–14814. 9 indexed citations
7.
Muthusubramanian, Shanmugam, et al.. (2013). Acid controlled generation of indanes and oxazolines from β-hydroxyarylethanamide. Tetrahedron Letters. 54(19). 2315–2320. 12 indexed citations
8.
Muthusubramanian, Shanmugam, et al.. (2012). Indium trichloride catalyzed regioselective synthesis of substituted pyrroles in water. Tetrahedron Letters. 54(14). 1779–1784. 37 indexed citations
9.
Muthusubramanian, Shanmugam, et al.. (2012). SnCl2-Catalyzed Selective Atom Economic Imino Diels–Alder Reaction: Synthesis of 2-(1H-Pyrrolo[2,3-b]pyridin-3-yl)quinolines. The Journal of Organic Chemistry. 77(3). 1468–1476. 43 indexed citations
10.
Sarkar, Asit R., et al.. (2012). A facile stereoselective synthesis of julolidine hybrid analogs via domino knoevenagel intramolecular hetero Diels–Alder reaction. Tetrahedron Letters. 53(14). 1748–1752. 14 indexed citations
11.
Jayashankaran, Jayadevan, et al.. (2010). Rhodium-Catalyzed Asymmetric Hydrosilylation of Ketones Employing a New Ligand Embodying the Bis(oxazolinyl)pyridine Moiety. Synlett. 2010(10). 1459–1462. 2 indexed citations
12.
Manickam, Govindaswamy, et al.. (2006). Selective one-pot synthesis of Z-iodoallylic iodides from propargyl alcohols. Tetrahedron Letters. 47(33). 5867–5868. 5 indexed citations
13.
Li, Yong, et al.. (2006). More Efficient Palladium Catalyst for Hydrogenolysis of Benzyl Groups. Synthetic Communications. 36(7). 925–928. 50 indexed citations
14.
15.
Manickam, Govindaswamy, et al.. (2000). Synthesis of Oligo(het)arylene Building Blocks with Bi- and Terpyridine Units. European Journal of Organic Chemistry. 2000(20). 3475–3481. 10 indexed citations
16.
Manickam, Govindaswamy & A. Dieter Schlüter. (2000). New Parts for a Construction Set of Bifunctional Oligo(het)arylene Building Blocks for Modular Chemistry. Synthesis. 2000(3). 442–446. 15 indexed citations
17.
Manickam, Govindaswamy & G. Sundararajan. (1999). Lithium bis[(1R,5R)-3-aza-3-benzyl-1,5-diphenylpentan-1,5-diolato]-aluminium — A new heterobimetallic catalyst for Michael addition reactions. Tetrahedron. 55(9). 2721–2736. 21 indexed citations
18.
Manickam, Govindaswamy & G. Sundararajan. (1999). Asymmetric Diels–Alder and ene reactions promoted by a Ti(IV) complex bearing a C2-symmetric tridentate ligand. Tetrahedron Asymmetry. 10(15). 2913–2925. 33 indexed citations
19.
Manickam, Govindaswamy & G. Sundararajan. (1997). Asymmetric induction in Michael addition reactions mediated by C 2 -symmetric aluminate. INDIAN JOURNAL OF CHEMISTRY- SECTION A. 36(6). 516–518.
20.
Manickam, Govindaswamy & G. Sundararajan. (1997). Asymmetric induction in Michael addition reactions mediated by C 2 -symmetrie aluminate. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 36(6). 516–518. 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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