In Howa Jeong

994 total citations
61 papers, 750 citations indexed

About

In Howa Jeong is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, In Howa Jeong has authored 61 papers receiving a total of 750 indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Organic Chemistry, 47 papers in Pharmaceutical Science and 5 papers in Molecular Biology. Recurrent topics in In Howa Jeong's work include Fluorine in Organic Chemistry (47 papers), Synthesis and Reactions of Organic Compounds (25 papers) and Synthesis and Biological Evaluation (9 papers). In Howa Jeong is often cited by papers focused on Fluorine in Organic Chemistry (47 papers), Synthesis and Reactions of Organic Compounds (25 papers) and Synthesis and Biological Evaluation (9 papers). In Howa Jeong collaborates with scholars based in South Korea, United States and India. In Howa Jeong's co-authors include Bum‐Tae Kim, Sung Lan Jeon, Seokjoon Lee, Sangtae Oh, Woon‐Seob Shin, Ji Hoon Choi, Yong Ki Min, Kwang Yun Cho, Boguslaw Mudryk and Theodore Cohen and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Organic Letters.

In The Last Decade

In Howa Jeong

58 papers receiving 711 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
In Howa Jeong South Korea 15 589 321 176 92 45 61 750
Sandrine Py France 22 1.1k 1.9× 124 0.4× 368 2.1× 148 1.6× 32 0.7× 52 1.2k
Ana C. Cuñat Spain 16 570 1.0× 112 0.3× 193 1.1× 57 0.6× 20 0.4× 45 781
Christian Gnamm Germany 12 1.0k 1.8× 86 0.3× 208 1.2× 245 2.7× 13 0.3× 17 1.1k
Radomir N. Saičić Serbia 18 965 1.6× 95 0.3× 202 1.1× 152 1.7× 27 0.6× 75 1.1k
Jean‐Bernard Behr France 21 984 1.7× 142 0.4× 586 3.3× 68 0.7× 19 0.4× 79 1.1k
Stephanie Meyer Germany 11 694 1.2× 159 0.5× 186 1.1× 125 1.4× 28 0.6× 14 819
Joseph Cs. Jászberényi United States 24 1.3k 2.2× 94 0.3× 276 1.6× 112 1.2× 29 0.6× 58 1.4k
Murugaiah A. M. Subbaiah India 14 808 1.4× 74 0.2× 184 1.0× 117 1.3× 19 0.4× 28 1.0k
Guillaume Bernadat France 21 992 1.7× 83 0.3× 403 2.3× 138 1.5× 63 1.4× 57 1.3k
Matthew Brichacek United States 11 1.2k 2.0× 142 0.4× 284 1.6× 222 2.4× 27 0.6× 20 1.4k

Countries citing papers authored by In Howa Jeong

Since Specialization
Citations

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

Fields of papers citing papers by In Howa Jeong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by In Howa Jeong. 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 In Howa Jeong. The network helps show where In Howa Jeong may publish in the future.

Co-authorship network of co-authors of In Howa Jeong

This figure shows the co-authorship network connecting the top 25 collaborators of In Howa Jeong. A scholar is included among the top collaborators of In Howa Jeong 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 In Howa Jeong. In Howa Jeong 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
2.
Kim, Sujin, et al.. (2016). Cross-coupling of 1,1-difluoro-1-en-3-yn-2-yl tosylates with arylboronic acids: A new approach to 2-aryl-1,1-difluoro-1,3-enynes. Journal of Fluorine Chemistry. 196. 67–71. 8 indexed citations
3.
Kim, Joo Hee, et al.. (2014). Synthesis of 2-aryl-1,1-difluoro-1,3-enynes via consecutive cross-coupling reactions of 2,2-difluoro-1-iodoethenyl p-toluenesulfonate. Journal of Fluorine Chemistry. 167. 166–171. 9 indexed citations
4.
Hwang, Ji Hye, et al.. (2011). Synthesis of novel 2-trifluoromethyl-1-methylene-3-phenylindene derivatives via carbocyclization reaction of 2-trifluoromethyl-1,1-diphenyl-1,3-enynes. Journal of Fluorine Chemistry. 132(12). 1227–1231. 13 indexed citations
5.
Choi, Ji Hoon & In Howa Jeong. (2008). A novel method for the synthesis of 2,2-diaryl-1,1-difluoroethenes. Tetrahedron Letters. 49(6). 952–955. 22 indexed citations
6.
Oh, Sangtae, In Howa Jeong, Woon‐Seob Shin, & Seokjoon Lee. (2004). Synthesis and antiangiogenic activity of exo-olefinated deoxoartemisinin derivatives. Bioorganic & Medicinal Chemistry Letters. 14(14). 3683–3686. 11 indexed citations
7.
Cheong, Chan Seong, et al.. (2003). Chemo-enzymatic synthesis of (R)-(+)-aminoglutethimide by kinetic resolution of (±)-4-cyano-4-phenyl-1-hexanol. Journal of Molecular Catalysis B Enzymatic. 26(3-6). 185–191. 4 indexed citations
8.
Jeong, In Howa, et al.. (2001). A NEW METHOD FOR THE PREPARATION OF 2,3-DIARYL-1,1-DIFLUORO-1,3-BUTADIENES. Synthetic Communications. 31(15). 2261–2270. 6 indexed citations
9.
Jeong, In Howa & Woo Jin Chung. (1999). The Novel Synthesis of Fluorinated Unsaturated Phosphonates. Bulletin of the Korean Chemical Society. 20(7). 768–770.
10.
Jeong, In Howa, et al.. (1999). Allylation Of Novel β-Phenylthio Substituted gem-Difluoroallylic Bromide to Carbonyl Compounds. Synthetic Communications. 29(2). 235–241. 4 indexed citations
11.
Jeong, In Howa, et al.. (1998). PREPARATION OF GEM-DIFLUORINATED BETA -PHENYLTHIO SUBSTITUTED ALLYLIC BROMIDES AND THEIR REACTIONS. Bulletin of the Korean Chemical Society. 19(6). 709–712.
12.
Jeong, In Howa, et al.. (1997). REACTION OF 1-SUBSTITUTED 2,2-DIFLUOROSTYRENE WITH DIANIONS OF BETA -ENAMINO KETONES. Bulletin of the Korean Chemical Society. 18(2). 135–137. 1 indexed citations
13.
Kim, Bum‐Tae, et al.. (1997). Reactions of 1-Substituted 2,2-Difluorostyrenes with Dianions of 1,3-Diketones: Novel Synthesis of 4H-Pyran-4-one Derivatives. Heterocycles. 45(1). 37–37. 2 indexed citations
14.
Jeong, In Howa, et al.. (1996). A new method for the preparation of perfluoroalkylated triphenylethylene derivatives. Tetrahedron Letters. 37(33). 5905–5908. 2 indexed citations
15.
Kim, Bum‐Tae, Yong Ki Min, Tadao Asami, et al.. (1995). Synthesis and biological activities of new fluorinated abscisic acid. Bioorganic & Medicinal Chemistry Letters. 5(3). 275–278. 19 indexed citations
16.
Jeong, In Howa, et al.. (1993). A Novel Procedure for the Synthesis of $\alpha,\beta$-Disubstituted $\beta$-Fluorovinyl and $\beta$-Trifluoromethylvinyl Sulfides. Bulletin of the Korean Chemical Society. 14(3). 309–311. 3 indexed citations
17.
Jeong, In Howa. (1992). Novel Synthesis of Fluorinated Vinyl 1,2-Bis-Sulfides. Bulletin of the Korean Chemical Society. 13(5). 468–469.
18.
Jeong, In Howa, et al.. (1991). Hetero Diels-Alder Reaction of Thebaine with Perfluoroaldehydes and Chemical Transformation of Their Adducts. Bulletin of the Korean Chemical Society. 12(2). 125–126. 8 indexed citations
19.
Jeong, In Howa, et al.. (1991). An Efficient and General Synthesis of Perfluoroalkyl Dithioketals. Bulletin of the Korean Chemical Society. 12(4). 355–356. 8 indexed citations
20.
Jeong, In Howa, et al.. (1990). Unexpected Effect of Fluorine in Diels-Alder Reaction of 2-Fluoroacrolein with Thebaine. Bulletin of the Korean Chemical Society. 11(3). 178–179. 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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