Shih‐Ching Chuang

2.4k total citations
83 papers, 2.0k citations indexed

About

Shih‐Ching Chuang is a scholar working on Organic Chemistry, Materials Chemistry and Electrical and Electronic Engineering. According to data from OpenAlex, Shih‐Ching Chuang has authored 83 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Organic Chemistry, 21 papers in Materials Chemistry and 17 papers in Electrical and Electronic Engineering. Recurrent topics in Shih‐Ching Chuang's work include Fullerene Chemistry and Applications (30 papers), Catalytic C–H Functionalization Methods (22 papers) and Synthesis and Properties of Aromatic Compounds (12 papers). Shih‐Ching Chuang is often cited by papers focused on Fullerene Chemistry and Applications (30 papers), Catalytic C–H Functionalization Methods (22 papers) and Synthesis and Properties of Aromatic Compounds (12 papers). Shih‐Ching Chuang collaborates with scholars based in Taiwan, United States and Japan. Shih‐Ching Chuang's co-authors include Chih‐Ping Chen, Chien‐Hong Cheng, Venkatachalam Rajeshkumar, Jayachandran Jayakumar, Yi‐Hsiang Chen, Kanniyappan Parthasarathy, Saeed I. Khan, Yves Rubin, Yasujiro Murata and Kôichi Komatsu and has published in prestigious journals such as Journal of the American Chemical Society, Advanced Materials and Angewandte Chemie International Edition.

In The Last Decade

Shih‐Ching Chuang

81 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shih‐Ching Chuang Taiwan 25 1.4k 480 397 255 141 83 2.0k
Denis Sh. Sabirov Russia 23 1.1k 0.8× 914 1.9× 148 0.4× 88 0.3× 51 0.4× 108 1.5k
W. Porter United States 16 256 0.2× 456 0.9× 138 0.3× 107 0.4× 139 1.0× 28 1.1k
Yoshiharu Sato Japan 26 1.0k 0.7× 894 1.9× 1.5k 3.7× 746 2.9× 222 1.6× 82 2.6k
Micheal Arockiaraj India 26 639 0.5× 359 0.7× 163 0.4× 45 0.2× 236 1.7× 108 1.8k
Jason W. Jones United States 18 1.2k 0.9× 673 1.4× 109 0.3× 180 0.7× 122 0.9× 49 1.7k
Yu‐ya Ohnishi Japan 18 408 0.3× 223 0.5× 118 0.3× 63 0.2× 189 1.3× 53 1.2k
Yuxiu Li China 19 943 0.7× 190 0.4× 179 0.5× 20 0.1× 223 1.6× 39 1.5k
Xing Gao China 20 175 0.1× 750 1.6× 707 1.8× 65 0.3× 25 0.2× 45 1.8k
Dragomir Stanisavljev Serbia 17 161 0.1× 100 0.2× 180 0.5× 174 0.7× 27 0.2× 59 776
Kjell Jorner Sweden 21 919 0.7× 935 1.9× 370 0.9× 53 0.2× 192 1.4× 44 1.8k

Countries citing papers authored by Shih‐Ching Chuang

Since Specialization
Citations

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

Fields of papers citing papers by Shih‐Ching Chuang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shih‐Ching Chuang. 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 Shih‐Ching Chuang. The network helps show where Shih‐Ching Chuang may publish in the future.

Co-authorship network of co-authors of Shih‐Ching Chuang

This figure shows the co-authorship network connecting the top 25 collaborators of Shih‐Ching Chuang. A scholar is included among the top collaborators of Shih‐Ching Chuang 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 Shih‐Ching Chuang. Shih‐Ching Chuang 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.
Chuang, Shih‐Ching, et al.. (2024). Synthesis of Benzo[c]cinnolinium Salts from 2-Azobiaryls by Copper(II) or Electrochemical Oxidation. Organic Letters. 26(8). 1694–1698. 1 indexed citations
2.
3.
Chuang, Shih‐Ching, et al.. (2021). Palladium-Catalyzed C–H Benzannulation of Functionalized Furans and Pyrroles with Alkynes. Synthesis. 53(17). 3001–3010. 3 indexed citations
4.
Chuang, Shih‐Ching, et al.. (2018). Phosphine‐Catalyzed Reactions with Unsaturated Carbonyl Compounds. Asian Journal of Organic Chemistry. 7(9). 1743–1757. 19 indexed citations
5.
Jayakumar, Jayachandran, et al.. (2014). One‐Pot Synthesis of Highly Substituted Polyheteroaromatic Compounds by Rhodium(III)‐Catalyzed Multiple CH Activation and Annulation. Angewandte Chemie International Edition. 53(37). 9889–9892. 147 indexed citations
6.
Chuang, Shih‐Ching, et al.. (2014). Nucleophilic conjugate 1,3-addition of phosphines to oligoynoates. Chemical Communications. 50(73). 10580–10580. 13 indexed citations
7.
Murata, Yasujiro, et al.. (2013). Recognition of hydrogen isotopomers by an open-cage fullerene. Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences. 371(1998). 20110629–20110629. 6 indexed citations
8.
Jayakumar, Jayachandran, et al.. (2013). One pot synthesis of bioactive benzopyranones through palladium-catalyzed C–H activation and CO insertion into 2-arylphenols. Chemical Communications. 49(100). 11797–11797. 66 indexed citations
9.
10.
Chuang, Shih‐Ching, et al.. (2011). Three-Component and Nonclassical Reaction of Phosphines with Enynes and Aldehydes: Formation of γ-Lactones Featuring α-Phosphorus Ylides. Organic Letters. 13(9). 2248–2251. 32 indexed citations
11.
Chen, Chang‐Hsiao, et al.. (2011). Comparison of extracellular signals between gold and carbon nanotubes based microelectrode arrays. 84. 2144–2147. 1 indexed citations
12.
Chen, Chih‐Ping, et al.. (2010). Organic photovoltaics incorporating fulleroisoquinolinones as n-type materials. Chemical Communications. 47(6). 1845–1847. 33 indexed citations
13.
Chuang, Shih‐Ching, et al.. (2010). Separation of open-cage fullerenes using nonaqueous capillary electrophoresis. Journal of Chromatography A. 1217(26). 4471–4475. 9 indexed citations
14.
15.
Sander, Michael, Thibaut Jarrosson, Shih‐Ching Chuang, Saeed I. Khan, & Yves Rubin. (2007). Approaches to Open Fullerenes:  Synthesis and Thermal Stability of cis-1 Bis(isobenzofuran) Diels−Alder Adducts of C60. The Journal of Organic Chemistry. 72(8). 2724–2731. 29 indexed citations
16.
Chuang, Shih‐Ching, et al.. (2007). Fine tuning of the orifice size of an open-cage fullerene by placing selenium in the rim: insertion/release of molecular hydrogen. Chemical Communications. 1278–1278. 32 indexed citations
17.
Chuang, Shih‐Ching, Saeed I. Khan, & Yves Rubin. (2006). Switch of Electronic Reactivity in Fullerene C60:  Activation of Threetrans-4Positions via Temporary Saturation of thecis-1Positions. Organic Letters. 8(26). 6075–6078. 8 indexed citations
18.
Chuang, Shih‐Ching, et al.. (2006). Photophysical Properties of a 1,2,3,4,5,6-Hexasubstituted Fullerene Derivative. The Journal of Physical Chemistry A. 110(51). 13662–13666. 10 indexed citations
19.
Xiang, Jing, Stephanie Holowka, & Shih‐Ching Chuang. (2004). Spatiotemporal analysis of neuromagnetic activation associated with mirror reading.. PubMed. 2004. 90–90. 7 indexed citations
20.
Chuang, Shih‐Ching. (1975). Homographic transformation for the simplification of discrete-time transfer functions by Padé approximation. International Journal of Control. 22(5). 721–728. 10 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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