Hyunik Shin

1.1k total citations
62 papers, 868 citations indexed

About

Hyunik Shin is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Hyunik Shin has authored 62 papers receiving a total of 868 indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Organic Chemistry, 14 papers in Molecular Biology and 7 papers in Pharmaceutical Science. Recurrent topics in Hyunik Shin's work include Synthesis and Characterization of Pyrroles (9 papers), Multicomponent Synthesis of Heterocycles (9 papers) and Catalytic C–H Functionalization Methods (8 papers). Hyunik Shin is often cited by papers focused on Synthesis and Characterization of Pyrroles (9 papers), Multicomponent Synthesis of Heterocycles (9 papers) and Catalytic C–H Functionalization Methods (8 papers). Hyunik Shin collaborates with scholars based in South Korea, United States and Germany. Hyunik Shin's co-authors include Sang‐gi Lee, Yu Sung Chun, Young Ok Ko, James D. White, A. W. Ruff, Tae‐Seong Kim, Neil S. Cutshall, Jeong‐Hun Sohn, Ju Hyun Kim and Kyuyoung Kim and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Hyunik Shin

56 papers receiving 827 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hyunik Shin South Korea 19 628 180 91 71 61 62 868
Wei‐Yi Ding China 13 521 0.8× 105 0.6× 16 0.2× 61 0.9× 16 0.3× 32 661
Katsuhiko Ueno Japan 14 306 0.5× 112 0.6× 28 0.3× 134 1.9× 9 0.1× 46 591
Annie B. H. Wong Singapore 10 116 0.2× 53 0.3× 73 0.8× 302 4.3× 30 0.5× 14 494
Clifford D. Bedford United States 15 316 0.5× 87 0.5× 72 0.8× 71 1.0× 44 0.7× 41 544
M. Ángeles García Spain 16 385 0.6× 82 0.5× 37 0.4× 144 2.0× 13 0.2× 43 680
S. Breda Portugal 13 239 0.4× 51 0.3× 80 0.9× 131 1.8× 10 0.2× 20 559
James E. Johnson United States 12 307 0.5× 130 0.7× 49 0.5× 65 0.9× 10 0.2× 46 649
Shaoxin Feng United States 10 117 0.2× 75 0.4× 36 0.4× 155 2.2× 16 0.3× 17 339
Bradley D. Gates United States 11 278 0.4× 49 0.3× 24 0.3× 73 1.0× 6 0.1× 17 443
Aniele Z. Tier Brazil 12 272 0.4× 53 0.3× 15 0.2× 89 1.3× 7 0.1× 14 454

Countries citing papers authored by Hyunik Shin

Since Specialization
Citations

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

Fields of papers citing papers by Hyunik Shin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hyunik Shin

This figure shows the co-authorship network connecting the top 25 collaborators of Hyunik Shin. A scholar is included among the top collaborators of Hyunik Shin 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 Hyunik Shin. Hyunik Shin 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.
Song, Ju‐Young, et al.. (2024). Proprietary Synthesis of the C27–C35 Fragment of Eribulin and Its Elaboration toward the C14–C35 Subunit. Organic Process Research & Development. 28(7). 2832–2843.
2.
Lee, Kee‐Young, et al.. (2021). Process Development of Tacalcitol. Organic Process Research & Development. 25(4). 982–987. 2 indexed citations
3.
Kim, Hyeji, Jihong Lee, Hyunik Shin, & Jeong‐Hun Sohn. (2018). Boric Ester and Thiourea as Coupling Partners in a Copper-Mediated Oxidative Dehydrosulfurative Carbon–Oxygen Cross-Coupling Reaction. Organic Letters. 20(7). 1961–1965. 12 indexed citations
4.
Phan, Nguyen Huu, Hyeji Kim, Hyunik Shin, Hee‐Seung Lee, & Jeong‐Hun Sohn. (2016). Dehydrosulfurative C–N Cross-Coupling and Concomitant Oxidative Dehydrogenation for One-Step Synthesis of 2-Aryl(alkyl)aminopyrimidines from 3,4-Dihydropyrimidin-1H-2-thiones. Organic Letters. 18(19). 5154–5157. 20 indexed citations
5.
Jeong, Sooyeon, et al.. (2015). Raman scattering studies of the lattice dynamics in layered MoS2. Journal of the Korean Physical Society. 66(10). 1575–1580. 16 indexed citations
6.
Shin, Hyunik, Sang‐gi Lee, Ju Han Kim, & Yu Sung Chun. (2012). Tandem Transformations of Nitriles into N-Heterocyclic Compounds by Electrophilic Trapping of Blaise Reaction Intermediates. Synthesis. 44(12). 1809–1817. 8 indexed citations
7.
8.
Ko, Young Ok, Yu Sung Chun, Youngmee Kim, et al.. (2010). Tandem one-pot synthesis of α-(aminomethylene)-γ-butyrolactones via regioselective epoxide ring-opening with the Blaise reaction intermediate. Tetrahedron Letters. 51(52). 6893–6896. 16 indexed citations
9.
Chun, Yu Sung, Young Ok Ko, Hyunik Shin, & Sang‐gi Lee. (2009). Tandem Blaise-Alkenylation with Unactivated Alkynes: One-Pot Synthesis of α-Vinylated β-Enaminoesters from Nitriles. Organic Letters. 11(15). 3414–3417. 30 indexed citations
10.
Ko, Young Ok, Yu Sung Chun, Youngmee Kim, et al.. (2009). An effective and general method for the highly regioselective synthesis of 1-phenylpyrazoles from β-enaminoketoesters, tandem Blaise–acylation adducts. Organic & Biomolecular Chemistry. 7(6). 1132–1132. 34 indexed citations
11.
12.
13.
Shin, Hyunik, et al.. (2008). Practical One-Pot Syntheses of Ethyl 4-Substituted-1H-Pyrrole-3-Carboxylates from Aldehydes. Organic Process Research & Development. 12(2). 291–293. 12 indexed citations
14.
Lee, Tae-Hee, Hyeong-Wook Choi, Young Keun Kim, et al.. (2006). Development of a Scalable Synthetic Route towards a Thrombin Inhibitor, LB30057. Organic Process Research & Development. 10(5). 881–886. 6 indexed citations
15.
Choi, Hyeong-Wook, et al.. (2005). Efficient and Scalable Synthesis of Ethyl 2,6-Dichloro-5-Fluoronicotinoyl Acetate Using the Blaise Reaction as a Key Step1. Organic Process Research & Development. 9(3). 311–313. 11 indexed citations
16.
Nam, Do Hyun, et al.. (2003). The Chemical Development of LB71350. Organic Process Research & Development. 7(6). 839–845. 7 indexed citations
17.
Nam, Do Hyun, et al.. (2002). Efficient Synthesis of 1-Substituted-5-Hydroxymethylimidazole Derivatives:  Clean Oxidative Cleavage of 2-Mercapto Group1. Organic Process Research & Development. 6(5). 674–676. 13 indexed citations
18.
Armstrong, R. W., A. W. Ruff, & Hyunik Shin. (1996). Elastic, plastic and cracking indentation behavior of silicon crystals. Materials Science and Engineering A. 209(1-2). 91–96. 23 indexed citations
19.
Ruff, A. W., Hyunik Shin, & C. J. Evans. (1995). Damage processes in ceramics resulting from diamond tool indentation and scratching in various environments. Wear. 181-183. 551–562. 23 indexed citations
20.
Armstrong, Ronald W., et al.. (1993). Elasticity, plasticity and cracking at indentations in single-crystal silicon. Journal of Materials Science Letters. 12(16). 1274–1275. 4 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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