Cheon‐Gyu Cho

2.8k total citations
93 papers, 2.4k citations indexed

About

Cheon‐Gyu Cho is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Cheon‐Gyu Cho has authored 93 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Organic Chemistry, 22 papers in Pharmacology and 13 papers in Molecular Biology. Recurrent topics in Cheon‐Gyu Cho's work include Chemical synthesis and alkaloids (36 papers), Catalytic C–H Functionalization Methods (23 papers) and Alkaloids: synthesis and pharmacology (21 papers). Cheon‐Gyu Cho is often cited by papers focused on Chemical synthesis and alkaloids (36 papers), Catalytic C–H Functionalization Methods (23 papers) and Alkaloids: synthesis and pharmacology (21 papers). Cheon‐Gyu Cho collaborates with scholars based in South Korea, United States and Vietnam. Cheon‐Gyu Cho's co-authors include Young‐Kwan Lim, Thành Tâm Nguyên, Kang-Sang Lee, Won‐Suk Kim, Gary H. Posner, Inji Shin, Haiwon Lee, Joon Ho Lee, Yuesheng Zhang and Paul Talalay 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

Cheon‐Gyu Cho

91 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cheon‐Gyu Cho South Korea 32 2.1k 414 282 161 160 93 2.4k
Uwe Rinner Austria 21 1.0k 0.5× 441 1.1× 321 1.1× 237 1.5× 155 1.0× 49 1.5k
Xiao‐Ming Zhang China 28 2.4k 1.1× 142 0.3× 263 0.9× 162 1.0× 114 0.7× 95 2.7k
Igor V. Magedov United States 24 1.6k 0.8× 100 0.2× 383 1.4× 308 1.9× 107 0.7× 52 1.8k
Shunsaku Ohta Japan 25 1.5k 0.7× 185 0.4× 315 1.1× 184 1.1× 59 0.4× 123 1.9k
Kiyoharu Nishide Japan 27 1.7k 0.8× 175 0.4× 572 2.0× 169 1.0× 87 0.5× 103 2.1k
Alakesh Bisai India 28 2.4k 1.1× 259 0.6× 448 1.6× 156 1.0× 65 0.4× 112 2.6k
Liisa T. Kanerva Finland 29 1.1k 0.5× 179 0.4× 2.2k 7.7× 48 0.3× 105 0.7× 128 2.7k
Steven W. M. Crossley United States 11 1.8k 0.9× 132 0.3× 443 1.6× 126 0.8× 154 1.0× 12 2.4k
Hisahiro Hagiwara Japan 31 2.7k 1.3× 144 0.3× 701 2.5× 279 1.7× 394 2.5× 199 3.6k
Razvan Simionescu Canada 17 545 0.3× 181 0.4× 311 1.1× 146 0.9× 93 0.6× 32 961

Countries citing papers authored by Cheon‐Gyu Cho

Since Specialization
Citations

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

Fields of papers citing papers by Cheon‐Gyu Cho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cheon‐Gyu Cho. 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 Cheon‐Gyu Cho. The network helps show where Cheon‐Gyu Cho may publish in the future.

Co-authorship network of co-authors of Cheon‐Gyu Cho

This figure shows the co-authorship network connecting the top 25 collaborators of Cheon‐Gyu Cho. A scholar is included among the top collaborators of Cheon‐Gyu Cho 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 Cheon‐Gyu Cho. Cheon‐Gyu Cho 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.
2.
Cho, Cheon‐Gyu, et al.. (2023). Divergent Asymmetric Total Syntheses of (−)-Alloaristoteline and (+)-Aristoteline via Directed Indolization Strategies. Organic Letters. 25(20). 3755–3759. 2 indexed citations
3.
Lee, Hyun‐Woo, et al.. (2022). Asymmetric Divergent Total Syntheses of (+)-Decursivine and (+)- Serotobenine via Intramolecular Fischer Indole Synthesis. Organic Letters. 24(15). 2873–2877. 5 indexed citations
4.
Cho, Cheon‐Gyu, et al.. (2020). Aminooxygenation of Ynamides with N-Hydroxybenzotriazoles: Synthesis of α-Benzotriazolyl Carbonyl Compounds. The Journal of Organic Chemistry. 85(11). 6935–6950. 15 indexed citations
5.
Youn, Ui Joung, et al.. (2018). Total Syntheses of Lobaric Acid and Its Derivatives from the Antarctic LichenStereocaulon alpinum. Journal of Natural Products. 81(6). 1460–1467. 14 indexed citations
6.
Lee, Joon Ho & Cheon‐Gyu Cho. (2018). H-Bonding Mediated Asymmetric Intramolecular Diels–Alder Reaction in the Formal Synthesis of (+)-Aplykurodinone-1. Organic Letters. 20(22). 7312–7316. 18 indexed citations
7.
8.
Park, Kyung, et al.. (2013). High‐Performance Air‐Stable Single‐Crystal Organic Nanowires Based on a New Indolocarbazole Derivative for Field‐Effect Transistors. Advanced Materials. 25(24). 3351–3356. 68 indexed citations
9.
Park, Jun Chul, et al.. (2012). Intramolecular Fischer Indole Synthesis and its Combination with an Aromatic [3,3]‐Sigmatropic Rearrangement for the Preparation of Tricyclic Benzo[cd]indoles. Angewandte Chemie International Edition. 51(10). 2496–2499. 61 indexed citations
10.
Kim, Rae-Kwon, Min-Jung Kim, Changhwan Yoon, et al.. (2012). A New 2-Pyrone Derivative, 5-Bromo-3-(3-hydroxyprop-1-ynyl)-2H-pyran-2-one, Suppresses Stemness in Glioma Stem-Like Cells. Molecular Pharmacology. 82(3). 400–407. 11 indexed citations
11.
Kim, Min-Jung, Rae-Kwon Kim, Changhwan Yoon, et al.. (2011). A new 2-pyrone derivative, 5-bromo-3-(3-hydroxyprop-1-ynyl)-2H-pyran-2-one, synergistically enhances radiation sensitivity in human cervical cancer cells. Anti-Cancer Drugs. 23(1). 43–50. 5 indexed citations
12.
Shin, Inji, et al.. (2007). Total Synthesis of (±)‐trans‐Dihydronarciclasine through a Highly endo‐Selective Diels–Alder Cycloaddition of 3,5‐Dibromo‐2‐pyrone. Angewandte Chemie International Edition. 46(13). 2303–2305. 84 indexed citations
13.
Choi, Young-Wook, Daewon Sohn, Won‐Suk Kim, et al.. (2004). Adsorption of alkanethiol molecules onto carbon nanotube surface. Journal of Vacuum Science & Technology B Microelectronics and Nanometer Structures Processing Measurement and Phenomena. 22(3). 1411–1415. 17 indexed citations
14.
Shin, Seunghoon, et al.. (2004). IMDA cycloadditions of 3-alkynyl tethered 2-pyrones for the synthesis of medium-sized macrocycles. Tetrahedron Letters. 45(30). 5857–5860. 21 indexed citations
15.
Cho, Cheon‐Gyu, et al.. (2003). Synthesis of tetrahydrofluorenes from the cycloadduct of 3-ethynyl-5-bromo-2-pyrone via cyclocarbopalladation reactions. Tetrahedron Letters. 44(24). 4439–4442. 9 indexed citations
16.
Kim, Kyuyoung, et al.. (2003). Cu(I) mediated one-pot synthesis of azobenzenes from bis-Boc aryl hydrazines and aryl halides. Tetrahedron Letters. 45(1). 117–120. 49 indexed citations
17.
18.
Cho, Cheon‐Gyu & Peter T. Lansbury. (1996). Synthesis of Two Bicyclic Surfactants Which Form Reversed Micelles Capable of Selective Protein Extraction. The Journal of Organic Chemistry. 61(6). 1920–1921. 3 indexed citations
19.
Zhang, Yuesheng, Cheon‐Gyu Cho, Gary H. Posner, & Paul Talalay. (1992). Spectroscopic quantitation of organic isothiocyanates by cyclocondensation with vicinal dithiols. Analytical Biochemistry. 205(1). 100–107. 128 indexed citations
20.
Cho, Cheon‐Gyu & Gary H. Posner. (1992). Alkyl and aryl isothiocyanates as masked primary amines. Tetrahedron Letters. 33(25). 3599–3602. 17 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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