Teh‐Chang Chou

610 total citations
44 papers, 492 citations indexed

About

Teh‐Chang Chou is a scholar working on Organic Chemistry, Materials Chemistry and Physical and Theoretical Chemistry. According to data from OpenAlex, Teh‐Chang Chou has authored 44 papers receiving a total of 492 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Organic Chemistry, 12 papers in Materials Chemistry and 7 papers in Physical and Theoretical Chemistry. Recurrent topics in Teh‐Chang Chou's work include Synthesis and Properties of Aromatic Compounds (11 papers), Oxidative Organic Chemistry Reactions (10 papers) and Synthetic Organic Chemistry Methods (9 papers). Teh‐Chang Chou is often cited by papers focused on Synthesis and Properties of Aromatic Compounds (11 papers), Oxidative Organic Chemistry Reactions (10 papers) and Synthetic Organic Chemistry Methods (9 papers). Teh‐Chang Chou collaborates with scholars based in Taiwan, United States and Germany. Teh‐Chang Chou's co-authors include Alan P. Marchand, Kung‐Ching Liao, Dick Van der Helm, Richard H. Mueller, Philip E. Eaton, Glenn R. Carlson, Kuan‐Jiuh Lin, Ren‐Tsung Wu, Chun‐Hung Wang and Yongjie Li and has published in prestigious journals such as Journal of the American Chemical Society, Chemistry of Materials and The Journal of Organic Chemistry.

In The Last Decade

Teh‐Chang Chou

44 papers receiving 475 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Teh‐Chang Chou Taiwan 13 401 116 79 63 46 44 492
Kyosuke Satake Japan 13 519 1.3× 176 1.5× 105 1.3× 85 1.3× 60 1.3× 76 680
Fodil Hamzaoui Algeria 15 420 1.0× 111 1.0× 124 1.6× 41 0.7× 27 0.6× 38 645
Mitsunori Oda Japan 12 540 1.3× 214 1.8× 82 1.0× 40 0.6× 44 1.0× 97 615
David H. Reid South Africa 13 556 1.4× 177 1.5× 100 1.3× 49 0.8× 55 1.2× 82 686
Helmi Neuvonen Finland 14 458 1.1× 58 0.5× 115 1.5× 140 2.2× 40 0.9× 30 631
Tatsuo Erabi Japan 12 196 0.5× 64 0.6× 44 0.6× 102 1.6× 45 1.0× 46 375
Toshiyuki Hamura Japan 19 915 2.3× 80 0.7× 117 1.5× 66 1.0× 43 0.9× 56 984
И. Е. Михайлов Russia 13 401 1.0× 176 1.5× 78 1.0× 44 0.7× 59 1.3× 89 547
Jorge L. Jios Argentina 15 415 1.0× 90 0.8× 69 0.9× 121 1.9× 30 0.7× 59 589
Kimiaki Yamamura Japan 15 399 1.0× 125 1.1× 80 1.0× 78 1.2× 43 0.9× 58 547

Countries citing papers authored by Teh‐Chang Chou

Since Specialization
Citations

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

Fields of papers citing papers by Teh‐Chang Chou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Teh‐Chang Chou. 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 Teh‐Chang Chou. The network helps show where Teh‐Chang Chou may publish in the future.

Co-authorship network of co-authors of Teh‐Chang Chou

This figure shows the co-authorship network connecting the top 25 collaborators of Teh‐Chang Chou. A scholar is included among the top collaborators of Teh‐Chang Chou 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 Teh‐Chang Chou. Teh‐Chang Chou 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.
Chou, Teh‐Chang, Jing‐Kai Huang, Sushilkumar S. Bahekar, & Ju‐Hsiou Liao. (2014). Quinoxaline-walled π-stacking molecules: synthesis, conformation, and luminescence properties. Tetrahedron. 70(44). 8361–8373. 3 indexed citations
2.
Chou, Teh‐Chang, et al.. (2012). Bicyclo[2.2.2]octene‐Based Molecular Tweezers and Cyclophanes. Journal of the Chinese Chemical Society. 59(3). 345–356. 1 indexed citations
3.
Chou, Teh‐Chang, et al.. (2011). Quinoxaline-Embedded Polyacenoquinone Esters: Synthesis, Electronic Properties, and Crystal Structure. Organic Letters. 13(17). 4588–4591. 8 indexed citations
4.
Chou, Teh‐Chang, Ren‐Tsung Wu, Kung‐Ching Liao, & Chun‐Hung Wang. (2011). N-1- and N-2-Anthryl Succinimide Derivatives: C–N Bond Rotational Behaviors and Fluorescence Energy Transfer. The Journal of Organic Chemistry. 76(16). 6813–6818. 15 indexed citations
5.
Chou, Teh‐Chang, et al.. (2009). Quinoxaline-based U-shaped septuple-bridged [7,7]orthocyclophanes: synthesis, solid-state structure, and self-assembly. Tetrahedron. 65(49). 10243–10257. 12 indexed citations
6.
Chou, Teh‐Chang, et al.. (2005). Synthesis and Luminescence Properties of U-Shaped Polycyclic Molecules Containing Syn-Facial Functionalized Quinoxaline Rings. Organic Letters. 7(22). 4843–4846. 21 indexed citations
7.
Liu, Ching‐Yang, et al.. (2004). Preparation and Luminescence Properties of Polymers Containing Dialkoxyacenes. Chemistry of Materials. 16(17). 3373–3380. 15 indexed citations
8.
Chou, Teh‐Chang, et al.. (2003). Synthesis and characterization of tetramethylene-syn-sesterbicyclo[2.2.2]octene. Tetrahedron. 59(9). 1493–1500. 2 indexed citations
9.
Chou, Teh‐Chang, et al.. (2000). Base‐Promoted Reaction of a Cage Diketone. Novel Rearrangement to a Tricyclic Bridgehead Olefin. Journal of the Chinese Chemical Society. 47(4B). 993–1000. 1 indexed citations
10.
11.
Chou, Teh‐Chang, et al.. (1999). Laticyclic Conjugated Polyenes. Study on Diels−Alder Cycloadditions of a Facially Dissymmetric Maleic Anhydride. The Journal of Organic Chemistry. 64(13). 4874–4883. 12 indexed citations
12.
Chou, Teh‐Chang, et al.. (1995). Syntheses and PE‐Spectroscopic Investigations of 2,6‐ and 3,5‐Bridged 1,4‐Dimethylidenecyclohexanes. Helvetica Chimica Acta. 78(8). 2011–2025. 1 indexed citations
13.
Chou, Teh‐Chang, et al.. (1994). Synthesis and Diels-Alder reactions of a facially dissymmetric tetracyclo-fused maleic anhydride with cyclic dienes. Tetrahedron Letters. 35(24). 4165–4168. 17 indexed citations
14.
Kuo, Sheng-Chu, et al.. (1991). 6-Pentadecylsalicylic Acid; An Antithrombin Component Isolated from the Stem ofRhus semialatavarroxburghii. Planta Medica. 57(3). 247–249. 17 indexed citations
15.
Chou, Teh‐Chang, et al.. (1991). An Expedient Synthesis ofendo-Tricyclo[5.2.2.02,6]undeca-4,8-dien-3-one. Synthetic Communications. 21(10-11). 1301–1306. 4 indexed citations
16.
Chou, Teh‐Chang, et al.. (1991). A diels-alder cycloaddition-cope rearrangement approach to the construction of Cs and C2-symmetric hexacycloeicosatetraendiones. Tetrahedron Letters. 32(44). 6351–6354. 5 indexed citations
17.
Kuo, Sheng‐Chu, et al.. (1989). Studies on heterocyclic compounds. VII. Syntheses of novel furo[2, 3‐b]chromones. Journal of Heterocyclic Chemistry. 26(3). 605–608. 5 indexed citations
18.
Chou, Teh‐Chang, et al.. (1986). Studies on Cage Compounds. Synthesis of 8,11‐Diazenediyl‐4,4‐Dimethoxy‐2,3,5,6‐Tetrachloropentacyclo[5.4.0.02,5.03,10.05,9]Undecane. Journal of the Chinese Chemical Society. 33(3). 227–234. 17 indexed citations
19.
20.
Marchand, Alan P., Teh‐Chang Chou, & Michael Barfield. (1975). Hexacyclo(5.4.0.02,6.04,11.05,9.08,10)undecane: A new C11H12 hydrocarbon. Tetrahedron Letters. 16(39). 3359–3362. 5 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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