Young Ho Rhee

2.6k total citations
84 papers, 2.1k citations indexed

About

Young Ho Rhee is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Young Ho Rhee has authored 84 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Organic Chemistry, 28 papers in Molecular Biology and 16 papers in Inorganic Chemistry. Recurrent topics in Young Ho Rhee's work include Synthetic Organic Chemistry Methods (36 papers), Carbohydrate Chemistry and Synthesis (26 papers) and Catalytic Alkyne Reactions (22 papers). Young Ho Rhee is often cited by papers focused on Synthetic Organic Chemistry Methods (36 papers), Carbohydrate Chemistry and Synthesis (26 papers) and Catalytic Alkyne Reactions (22 papers). Young Ho Rhee collaborates with scholars based in South Korea, United States and Japan. Young Ho Rhee's co-authors include Barry M. Trost, Hae Jin Kim, Jaiwook Park, Jungjoon Kim, Olivier Dirat, Janet L. Gunzner, Soyeong Kang, Baburaj Baskar, Sreya Gupta and Mijin Kim and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Analytical Chemistry.

In The Last Decade

Young Ho Rhee

81 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Young Ho Rhee South Korea	24	2.0k	397	381	161	157	84	2.1k
Gregory R. Dake Canada	26	1.7k 0.9×	363 0.9×	360 0.9×	172 1.1×	80 0.5×	49	1.9k
Marie E. Krafft United States	29	2.1k 1.1×	395 1.0×	329 0.9×	65 0.4×	147 0.9×	87	2.3k
Dirk Gördes Germany	22	933 0.5×	364 0.9×	465 1.2×	130 0.8×	87 0.6×	36	1.4k
Gordon Brasche Germany	8	3.2k 1.6×	346 0.9×	484 1.3×	179 1.1×	69 0.4×	9	3.3k
Yong Qiang Tu China	26	2.4k 1.2×	617 1.6×	506 1.3×	193 1.2×	216 1.4×	66	2.9k
Charles Fehr Switzerland	26	1.6k 0.8×	428 1.1×	407 1.1×	64 0.4×	95 0.6×	59	1.8k
Jun‐ichi Matsuo Japan	27	2.1k 1.1×	344 0.9×	348 0.9×	101 0.6×	80 0.5×	112	2.3k
Geneviève Balme France	32	2.9k 1.5×	275 0.7×	384 1.0×	175 1.1×	45 0.3×	92	3.0k
Yoshiro Hirai Japan	23	1.2k 0.6×	139 0.4×	279 0.7×	117 0.7×	108 0.7×	99	1.4k
Roberto Fernández de la Pradilla Spain	25	2.2k 1.1×	241 0.6×	558 1.5×	79 0.5×	105 0.7×	121	2.4k

Countries citing papers authored by Young Ho Rhee

Since Specialization

Citations

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

Fields of papers citing papers by Young Ho Rhee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Young Ho Rhee. 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 Young Ho Rhee. The network helps show where Young Ho Rhee may publish in the future.

Co-authorship network of co-authors of Young Ho Rhee

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

All Works

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20 of 20 papers shown

Lee, Jeong Min, et al.. (2021). Generation of N–H Imines from α-Azidocarboxylic Acids through Ru-Catalyzed Decarboxylation. The Journal of Organic Chemistry. 86(23). 17409–17417. 2 indexed citations

Jang, Dong‐Jin, et al.. (2021). Palladium‐Catalyzed Asymmetric Decarboxylative Addition of β‐Keto Acids to Heteroatom‐Substituted Allenes. Angewandte Chemie. 133(41). 22340–22345. 6 indexed citations

Lee, Jeong Min, et al.. (2020). Concurrent Formation of N–H Imines and Carbonyl Compounds by Ruthenium-Catalyzed C–C Bond Cleavage of β-Hydroxy Azides. Organic Letters. 22(12). 4608–4613. 7 indexed citations

Kang, Jihun, et al.. (2019). Flexible Total Synthesis of 11‐Deoxylandomycins and Their Non‐Natural Analogues by Way of Asymmetric Metal Catalysis. Angewandte Chemie. 132(6). 2369–2373. 8 indexed citations

Garnsey, Michelle R., Yuriy Slutskyy, Christopher R. Jamison, et al.. (2017). Short Enantioselective Total Syntheses of Cheloviolenes A and B and Dendrillolide C via Convergent Fragment Coupling Using a Tertiary Carbon Radical. The Journal of Organic Chemistry. 83(13). 6958–6976. 44 indexed citations

Slutskyy, Yuriy, et al.. (2017). Versatile Construction of 6-Substituted cis-2,8-Dioxabicyclo[3.3.0]octan-3-ones: Short Enantioselective Total Syntheses of Cheloviolenes A and B and Dendrillolide C. Journal of the American Chemical Society. 139(21). 7192–7195. 46 indexed citations

Park, Jin Yong, et al.. (2017). Ruthenium Bisammine Complex and Its Reaction with Aryl Azides. Organometallics. 36(18). 3471–3476. 15 indexed citations

Jeon, Mina, et al.. (2015). Synthesis of Enamides by Ruthenium‐Catalyzed Reaction of Alkyl Azides with Acid Anhydrides in Ionic Liquid. ChemCatChem. 7(24). 4030–4034. 17 indexed citations

Jeon, Mina, et al.. (2015). Synthesis of 1H-azadienes and application to one-pot organic transformations. RSC Advances. 6(1). 661–668. 6 indexed citations

10.

Jeon, Mina, et al.. (2015). Fast and Complete Transimination of NH Imines into O‐Alkyl Oximes. Asian Journal of Organic Chemistry. 4(4). 316–319. 7 indexed citations

11.

Kang, Soyeong, et al.. (2014). Access to trans‐3,4‐Dihydroxy‐2‐alkylpyrrolidines and Piperidines by Use of Stereodefined Cyclic N,O‐Acetals as a Diversity‐Generating Element. Chemistry - A European Journal. 20(49). 16391–16396. 8 indexed citations

12.

Kim, Hae Jin, et al.. (2012). Synthetic Strategy for Cyclic Amines: A Stereodefined Cyclic N,O‐Acetal as a Stereocontrol and Diversity‐Generating Element. Angewandte Chemie International Edition. 51(48). 12055–12058. 58 indexed citations

13.

Seo, Jongcheol, et al.. (2011). Aliphatic dipeptide tags for multi-2-plex protein quantification. The Analyst. 136(8). 1614–1614. 4 indexed citations

14.

Rhee, Young Ho, et al.. (2011). Gold(I)‐Catalyzed Access to Tetrahydropyran‐4‐ones from 4‐(Alkoxyalkyl)oxy‐1‐butynes: Formal Catalytic Petasis–Ferrier Rearrangement. Chemistry - A European Journal. 17(5). 1433–1436. 29 indexed citations

15.

Rhee, Young Ho, et al.. (2011). A racemic formal total synthesis of clavukerin A using gold(I)-catalyzed cycloisomerization of 3-methoxy-1,6-enynes as the key strategy. Beilstein Journal of Organic Chemistry. 7. 740–743. 6 indexed citations

16.

Baskar, Baburaj, et al.. (2009). Gold(I)‐Catalyzed Synthesis of Highly Substituted 2‐Cyclopentenones from 5‐Siloxypent‐3‐en‐1‐ynes. Chemistry - A European Journal. 15(44). 11837–11841. 24 indexed citations

17.

Baskar, Baburaj, et al.. (2008). Gold(I)‐Catalyzed Cycloisomerization of 3‐Methoxy‐1,6‐enynes Featuring Tandem Cyclization and [3,3]‐Sigmatropic Rearrangement. Angewandte Chemie International Edition. 47(12). 2263–2266. 88 indexed citations

18.

Chung, Cheol K., et al.. (1999). A Facile Synthesis of Methyl (3-isocyano-2-cyclopent-2-enyl) acetate. Bulletin of the Korean Chemical Society. 20(1). 99–100. 1 indexed citations

19.

Lee, Eun, et al.. (1993). 5-($\pi$-Endo)-exo Vinyl Radical Cyclization Mediated by the Addition of Stannly Radicals to Triples Bonds. Bulletin of the Korean Chemical Society. 14(5). 542–543.

20.

Honda, Kazuki, et al.. (1990). Chronic intake of Panax ginseng extract stabilizes sleep and wakefulness in food-deprived rats. Neuroscience Letters. 111(1-2). 217–221. 23 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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