Chang‐Woo Cho

2.0k total citations
59 papers, 1.7k citations indexed

About

Chang‐Woo Cho is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Chang‐Woo Cho has authored 59 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Organic Chemistry, 20 papers in Molecular Biology and 11 papers in Inorganic Chemistry. Recurrent topics in Chang‐Woo Cho's work include Asymmetric Synthesis and Catalysis (22 papers), Synthesis and Catalytic Reactions (13 papers) and Synthetic Organic Chemistry Methods (13 papers). Chang‐Woo Cho is often cited by papers focused on Asymmetric Synthesis and Catalysis (22 papers), Synthesis and Catalytic Reactions (13 papers) and Synthetic Organic Chemistry Methods (13 papers). Chang‐Woo Cho collaborates with scholars based in South Korea, United States and China. Chang‐Woo Cho's co-authors include Michael J. Krische, Kyo Han Ahn, Sunwoo Lee, Jaiwook Park, Jongrock Kong, Hyo‐Jun Lee, Sung Hwa Jhung, Biswa Nath Bhadra, Jungkyu K. Lee and Su‐Jeong Lee and has published in prestigious journals such as Angewandte Chemie International Edition, PLoS ONE and Chemical Communications.

In The Last Decade

Chang‐Woo Cho

59 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chang‐Woo Cho South Korea 23 1.2k 525 470 149 142 59 1.7k
Kosuke Namba Japan 24 1.2k 1.1× 183 0.3× 311 0.7× 170 1.1× 145 1.0× 110 1.7k
Renhua Liu China 22 1.7k 1.4× 416 0.8× 260 0.6× 96 0.6× 351 2.5× 58 2.2k
Bin Fu China 25 1.3k 1.1× 374 0.7× 387 0.8× 67 0.4× 167 1.2× 98 1.8k
Béchir Ben Hassine Tunisia 21 1.3k 1.1× 248 0.5× 286 0.6× 58 0.4× 429 3.0× 113 1.6k
Alain Valleix France 23 771 0.7× 307 0.6× 485 1.0× 52 0.3× 182 1.3× 49 1.6k
Pedro Ramírez‐López Spain 21 1.3k 1.1× 326 0.6× 218 0.5× 72 0.5× 92 0.6× 41 1.5k
Claude Lion France 17 752 0.6× 197 0.4× 149 0.3× 203 1.4× 158 1.1× 111 1.3k
Luminiţa Silaghi‐Dumitrescu Romania 18 652 0.6× 311 0.6× 158 0.3× 54 0.4× 157 1.1× 106 1.1k
Claude Y. Legault Canada 29 2.4k 2.1× 799 1.5× 359 0.8× 68 0.5× 205 1.4× 71 3.1k

Countries citing papers authored by Chang‐Woo Cho

Since Specialization
Citations

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

Fields of papers citing papers by Chang‐Woo Cho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chang‐Woo Cho

This figure shows the co-authorship network connecting the top 25 collaborators of Chang‐Woo Cho. A scholar is included among the top collaborators of Chang‐Woo 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 Chang‐Woo Cho. Chang‐Woo 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.
Kim, Bora, et al.. (2021). Synthesis of TKX‐50 via 2‐Methoxyisopropyl‐Protected Diazidoglyoxime as an Insensitive Intermediate. Propellants Explosives Pyrotechnics. 46(5). 732–736. 4 indexed citations
2.
3.
Bhadra, Biswa Nath, Jungkyu K. Lee, Chang‐Woo Cho, & Sung Hwa Jhung. (2018). Remarkably efficient adsorbent for the removal of bisphenol A from water: Bio-MOF-1-derived porous carbon. Chemical Engineering Journal. 343. 225–234. 144 indexed citations
4.
Lee, Doohyun, Kwang‐Hyeon Liu, Sangkyu Lee, et al.. (2015). Efficient Syntheses of 1,2,3-Triazoloamide Derivatives Using Solid- and Solution-Phase Synthetic Approaches. Molecules. 20(11). 19984–20013. 7 indexed citations
5.
Lee, Su‐Jeong, et al.. (2014). Cinchona-based primary amine-catalyzed enantioselective aza-Michael reactions of pyrroles with α,β-unsaturated aldehydes. Tetrahedron Asymmetry. 25(20-21). 1383–1388. 16 indexed citations
6.
Chung, Eunsook, et al.. (2013). Overexpression of VrUBC1, a Mung Bean E2 Ubiquitin-Conjugating Enzyme, Enhances Osmotic Stress Tolerance in Arabidopsis. PLoS ONE. 8(6). e66056–e66056. 65 indexed citations
7.
Lee, Yohan, Seongwan Jang, Chang‐Woo Cho, et al.. (2013). Recyclable Rhodium Nanoparticles: Green Hydrothermal Synthesis, Characterization, and Highly Catalytic Performance in Reduction of Nitroarenes. Journal of Nanoscience and Nanotechnology. 13(11). 7477–7481. 10 indexed citations
8.
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Kim, Chong‐Hyeak, et al.. (2012). Synthesis and Herbicidal Activities of Enantiopure Methiozolins. Bulletin of the Korean Chemical Society. 33(1). 297–300. 7 indexed citations
10.
Chung, Eunsook, Chang‐Woo Cho, Soonok Kim, et al.. (2012). Molecular cloning and characterization of RNA binding protein genes from the wild radish. Genes & Genomics. 34(6). 663–669. 1 indexed citations
11.
Lee, Su‐Jeong, et al.. (2011). Organocatalytic enantioselective formal synthesis of bromopyrrole alkaloids via aza-Michael addition. Organic & Biomolecular Chemistry. 9(22). 7734–7734. 32 indexed citations
12.
Chung, Eunsook, et al.. (2011). Exploration for the salt stress tolerance genes from a salt-treated halophyte, Suaeda asparagoides. Plant Cell Reports. 31(1). 35–48. 32 indexed citations
13.
Lee, Hyo‐Jun & Chang‐Woo Cho. (2011). Chemoselective Suzuki Cross-Coupling Reactions of Chiral Pyrrolizines. Bulletin of the Korean Chemical Society. 32(1). 359–362. 6 indexed citations
14.
Lee, Hyo‐Jun, et al.. (2011). Concise Asymmetric Formal Synthesis of Pyrrolopiperazinone Natural Products by Tandem Cross Metathesis/Intramolecular Aza-Conjugate Addition. Bulletin of the Korean Chemical Society. 32(1). 315–318. 12 indexed citations
15.
16.
Lee, Jai‐Heon, Chang‐Woo Cho, Ji-Yeon Hwang, et al.. (2008). Amelioration of Plasma Glucose and Cholesterol levels in Db/db Mice by a Mixture of Chinese Herbs. Korean Journal of Medicinal Crop Science. 16(4). 225–230. 3 indexed citations
17.
Cho, Chang‐Woo, Eduardas Skucas, & Michael J. Krische. (2007). Contrasteric Regiocontrol in Rhodium-Catalyzed Hydrogenative Couplings of Nonsymmetric 1,3-Diynes to Ethyl Glyoxalate. Organometallics. 26(15). 3860–3867. 9 indexed citations
18.
Hwang, Ji-Yeon, Soo‐Kyung Lee, Mi-Eun Kim, et al.. (2007). Hypolipidemic effect of Salicornia herbacea in animal model of type 2 diabetes mellitus. Nutrition Research and Practice. 1(4). 371–371. 17 indexed citations
19.
Cho, Chang‐Woo & Michael J. Krische. (2004). Regio‐ and Stereoselective Construction of γ‐Butenolides through Phosphine‐Catalyzed Substitution of Morita–Baylis–Hillman Acetates: An Organocatalytic Allylic Alkylation. Angewandte Chemie International Edition. 43(48). 6689–6691. 162 indexed citations
20.
Kim, Sung‐Gon, Chang‐Woo Cho, & Kyo Han Ahn. (1999). Chiral biferrocene-based bis(oxazolines): Ligands for Cu(I)-catalyzed asymmetric cyclopropanations of ene-diazoacetates. Tetrahedron. 55(33). 10079–10086. 19 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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