Jungha Chae

796 total citations
17 papers, 668 citations indexed

About

Jungha Chae is a scholar working on Organic Chemistry, Pharmaceutical Science and Inorganic Chemistry. According to data from OpenAlex, Jungha Chae has authored 17 papers receiving a total of 668 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 13 papers in Pharmaceutical Science and 3 papers in Inorganic Chemistry. Recurrent topics in Jungha Chae's work include Fluorine in Organic Chemistry (13 papers), Catalytic C–H Functionalization Methods (10 papers) and Catalytic Cross-Coupling Reactions (6 papers). Jungha Chae is often cited by papers focused on Fluorine in Organic Chemistry (13 papers), Catalytic C–H Functionalization Methods (10 papers) and Catalytic Cross-Coupling Reactions (6 papers). Jungha Chae collaborates with scholars based in Japan, United Kingdom and Australia. Jungha Chae's co-authors include Tsutomu Konno, Takashi Ishihara, Hiroki Yamanaka, Yoshitaka Hamashima, P. Andrew Evans, Ryo Shimizu, Hiromichi Egami, Mikiko Sodeoka, Samuel J. Oliver and Tomoo Tanaka and has published in prestigious journals such as Journal of the American Chemical Society, Applied Physics Letters and Chemical Communications.

In The Last Decade

Jungha Chae

17 papers receiving 649 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jungha Chae Japan 14 533 413 207 76 20 17 668
Heng‐Ying Xiong China 12 664 1.2× 397 1.0× 185 0.9× 67 0.9× 19 0.9× 29 747
Dhande Sudhakar Reddy Japan 9 420 0.8× 259 0.6× 128 0.6× 78 1.0× 17 0.8× 12 459
Sergio Pascual Spain 13 554 1.0× 127 0.3× 117 0.6× 46 0.6× 14 0.7× 18 569
Christophe Audouard France 10 416 0.8× 325 0.8× 112 0.5× 147 1.9× 11 0.6× 16 459
Yuanyao Xu China 14 547 1.0× 211 0.5× 184 0.9× 87 1.1× 13 0.7× 18 591
Habiba Vaghoo United States 11 408 0.8× 215 0.5× 129 0.6× 91 1.2× 19 0.9× 13 487
Alexandra E. Strom United States 7 595 1.1× 330 0.8× 227 1.1× 71 0.9× 36 1.8× 9 695
Desta Doro Bume United States 11 427 0.8× 296 0.7× 73 0.4× 80 1.1× 18 0.9× 12 535
Kui Liao China 11 493 0.9× 160 0.4× 154 0.7× 92 1.2× 7 0.3× 11 528
Takao Horikawa Japan 5 455 0.9× 316 0.8× 127 0.6× 68 0.9× 6 0.3× 6 478

Countries citing papers authored by Jungha Chae

Since Specialization
Citations

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

Fields of papers citing papers by Jungha Chae

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jungha Chae

This figure shows the co-authorship network connecting the top 25 collaborators of Jungha Chae. A scholar is included among the top collaborators of Jungha Chae 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 Jungha Chae. Jungha Chae is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Turnbull, Ben W. H., Jungha Chae, Samuel J. Oliver, & P. Andrew Evans. (2017). Regio- and stereospecific rhodium-catalyzed allylic alkylation with an acyl anion equivalent: an approach to acyclic α-ternary β,γ-unsaturated aryl ketones. Chemical Science. 8(5). 4001–4005. 16 indexed citations
2.
Jung, Youngsuk, et al.. (2013). Adhesion of a fluorinated poly(amic acid) with stainless steel surfaces. Applied Physics Letters. 102(3). 4 indexed citations
3.
Evans, P. Andrew, Samuel J. Oliver, & Jungha Chae. (2012). Rhodium-Catalyzed Allylic Substitution with an Acyl Anion Equivalent: Stereospecific Construction of Acyclic Quaternary Carbon Stereogenic Centers. Journal of the American Chemical Society. 134(47). 19314–19317. 65 indexed citations
4.
Shimizu, Ryo, et al.. (2010). Direct C2-trifluoromethylation of indole derivatives catalyzed by copper acetate. Tetrahedron Letters. 51(45). 5947–5949. 158 indexed citations
5.
Chae, Jungha. (2008). Recent Catalytic C-H Functionalization by Carbenoid Insertion in Non-Conventional Media. Journal of Synthetic Organic Chemistry Japan. 66(12). 1223–1224. 1 indexed citations
6.
Konno, Tsutomu, et al.. (2005). Regioselective One-Step Synthesis of 4-Fluoroalkylated Isoquinolines via Carbopalladation Reaction of Fluorine-Containing Alkynes. The Journal of Organic Chemistry. 70(24). 10172–10174. 38 indexed citations
7.
Konno, Tsutomu, Jungha Chae, Tomoo Tanaka, Takashi Ishihara, & Hiroki Yamanaka. (2005). Highly regio- and stereoselective hydrometallation reactions of fluorine-containing internal alkynes: Novel approaches to fluoroalkylated alkenes. Journal of Fluorine Chemistry. 127(1). 36–43. 29 indexed citations
8.
Konno, Tsutomu, et al.. (2005). Highly regio- and stereo-selective carbometallation reaction of fluorine-containing internal acetylenes with organocopper reagents. Tetrahedron. 61(39). 9391–9404. 19 indexed citations
9.
Konno, Tsutomu, Jungha Chae, Tomoo Tanaka, Takashi Ishihara, & Hiroki Yamanaka. (2004). A sequential highly stereoselective hydroboration and Suzuki–Miyaura cross-coupling reaction of fluoroalkylated internal acetylenes: a practical one-pot synthesis of fluoroalkylated trisubstituted alkenes. Chemical Communications. 690–691. 34 indexed citations
10.
Konno, Tsutomu, Jungha Chae, Takashi Ishihara, & Hiroki Yamanaka. (2004). A first regioselective synthesis of 3-fluoroalkylated benzofurans via palladium-catalyzed annulation of fluorine-containing internal alkynes with variously substituted 2-iodophenol. Tetrahedron. 60(51). 11695–11700. 40 indexed citations
11.
12.
Chae, Jungha, Tsutomu Konno, Takashi Ishihara, & Hiroki Yamanaka. (2004). A Facile Synthesis of Various Fluorine-Containing Indole Derivatives via Palladium-Catalyzed Annulation of Internal Alkynes. Chemistry Letters. 33(3). 314–315. 40 indexed citations
13.
Konno, Tsutomu, et al.. (2004). Highly Regio- and Stereoselective Carbostannylation Reaction of Fluorine-Containing Internal Acetylenes with Allylstannanes. The Journal of Organic Chemistry. 69(6). 2188–2190. 15 indexed citations
14.
15.
Konno, Tsutomu, Jungha Chae, Takashi Ishihara, & Hiroki Yamanaka. (2004). A Facile Regiocontrol in the Palladium-Catalyzed Annulation of Fluorine-Containing Internal Alkynes with Variously Substituted 2-Iodoanilines:  A New Regioselective Synthesis of 2- or 3-Fluoroalkylated Indole Derivatives. The Journal of Organic Chemistry. 69(24). 8258–8265. 55 indexed citations
16.
Chae, Jungha, et al.. (2003). A highly regio- and stereo-selective hydrostannation reaction of various fluorine-containing internal acetylene derivatives. Journal of Fluorine Chemistry. 120(2). 185–193. 23 indexed citations
17.
Konno, Tsutomu, et al.. (2003). Facile syntheses of various per- or polyfluoroalkylated internal acetylene derivatives. Tetrahedron. 59(38). 7571–7580. 65 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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