Sangtae Oh

450 total citations
28 papers, 361 citations indexed

About

Sangtae Oh is a scholar working on Organic Chemistry, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Sangtae Oh has authored 28 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 10 papers in Molecular Biology and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Sangtae Oh's work include Malaria Research and Control (6 papers), Click Chemistry and Applications (5 papers) and Synthesis and Catalytic Reactions (5 papers). Sangtae Oh is often cited by papers focused on Malaria Research and Control (6 papers), Click Chemistry and Applications (5 papers) and Synthesis and Catalytic Reactions (5 papers). Sangtae Oh collaborates with scholars based in South Korea, United States and Bangladesh. Sangtae Oh's co-authors include Seokjoon Lee, Woon‐Seob Shin, In Howa Jeong, Jungyeob Ham, Chan Mug Ahn, Qian Wang, Daeho Kwon, Gab-Man Park, Sangkyu Park and J. W. Wheeler and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

Sangtae Oh

28 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sangtae Oh South Korea 12 169 143 45 41 33 28 361
Rakesh R. Somani India 12 188 1.1× 146 1.0× 20 0.4× 16 0.4× 8 0.2× 43 412
Kamal Ahmad India 14 270 1.6× 228 1.6× 71 1.6× 15 0.4× 15 0.5× 40 591
Aaron DeBono Australia 13 108 0.6× 174 1.2× 59 1.3× 46 1.1× 6 0.2× 14 347
Supriyo Saha India 13 141 0.8× 155 1.1× 13 0.3× 23 0.6× 22 0.7× 52 378
Asghar Davood Iran 12 271 1.6× 144 1.0× 39 0.9× 35 0.9× 18 0.5× 57 453
Chatchakorn Eurtivong Thailand 15 187 1.1× 224 1.6× 18 0.4× 10 0.2× 13 0.4× 41 468
Ahmad Alzamami Saudi Arabia 12 83 0.5× 158 1.1× 14 0.3× 18 0.4× 13 0.4× 24 347
Jerome P. L. Ng Macao 11 97 0.6× 117 0.8× 51 1.1× 23 0.6× 7 0.2× 28 324
Ashish Wadhwani India 11 75 0.4× 131 0.9× 27 0.6× 9 0.2× 19 0.6× 30 391
Zaesung No South Korea 15 248 1.5× 313 2.2× 112 2.5× 8 0.2× 20 0.6× 34 630

Countries citing papers authored by Sangtae Oh

Since Specialization
Citations

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

Fields of papers citing papers by Sangtae Oh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sangtae Oh

This figure shows the co-authorship network connecting the top 25 collaborators of Sangtae Oh. A scholar is included among the top collaborators of Sangtae Oh 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 Sangtae Oh. Sangtae Oh 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.
Lee, Dong Hwan, M. Hasanuzzaman, Daeho Kwon, et al.. (2019). 10-Phenyltriazoyl Artemisinin is a Novel P-glycoprotein Inhibitor that Suppresses the Overexpression and Function of P-glycoprotein. Current Pharmaceutical Design. 24(46). 5590–5597. 8 indexed citations
2.
Park, Gab-Man, et al.. (2017). Antimalarial Activity of C-10 Substituted Triazolyl Artemisinin. Korean Journal of Parasitology. 55(6). 661–665. 6 indexed citations
4.
Ahn, Chan Mug, Sangtae Oh, Daeho Kwon, et al.. (2015). Synthesis of alkylsulfonyl and substituted benzenesulfonyl curcumin mimics as dual antagonist of L-type Ca2+ channel and endothelin A/B2 receptor. Bioorganic & Medicinal Chemistry. 23(20). 6673–6682. 11 indexed citations
5.
Oh, Sangtae, et al.. (2014). Synthesis of diethylamino-curcumin mimics with substituted triazolyl groups and their sensitization effect of TRAIL against brain cancer cells. Bioorganic & Medicinal Chemistry Letters. 24(15). 3346–3350. 16 indexed citations
6.
Oh, Sangtae, et al.. (2013). Anti-platelet Aggregation and Anti-thrombotic Effects of Marine Natural Products Sargahydroquinoic Acid and Sargaquinoic Acid. Bulletin of the Korean Chemical Society. 34(10). 3121–3124. 3 indexed citations
7.
Shin, Woon‐Seob, Sangtae Oh, Gab-Man Park, et al.. (2013). 5E- and 5Z-farnesylacetones from Sargassum siliquastrum as novel selective L-type calcium channel blockers. Vascular Pharmacology. 58(4). 299–306. 7 indexed citations
8.
Park, Sangkyu, Sangtae Oh, Hye Kyoung Shin, et al.. (2011). Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis. Bioorganic & Medicinal Chemistry Letters. 21(12). 3573–3577. 22 indexed citations
9.
Oh, Sangtae, Woon‐Seob Shin, Jungyeob Ham, & Seokjoon Lee. (2011). Synthesis of Artemisinins with Substituted Sulfidyl or Sulfonyl Moiety and Their Anti-angiogenesis Activity. Bulletin of the Korean Chemical Society. 32(8). 2823–2826. 4 indexed citations
10.
Oh, Sangtae, et al.. (2010). Synthesis of two marine farnesylacetones that dilate the basilar arteries of rabbits. Bioorganic & Medicinal Chemistry Letters. 20(14). 4206–4209. 4 indexed citations
11.
Oh, Sangtae, et al.. (2010). Acid-catalyzed synthesis of 10-substituted triazolyl artemisinins and their growth inhibitory activity against various cancer cells. Bioorganic & Medicinal Chemistry Letters. 20(14). 4112–4115. 25 indexed citations
12.
Oh, Sangtae, et al.. (2008). Synthesis of 10-substituted triazolyl artemisinins possessing anticancer activity via Huisgen 1,3-dipolar cylcoaddition. Bioorganic & Medicinal Chemistry Letters. 19(2). 382–385. 52 indexed citations
13.
Oh, Sangtae, In Howa Jeong, Woon‐Seob Shin, Qian Wang, & Seokjoon Lee. (2005). Synthesis and biological activity of (+)-hedychilactone A and its analogs from (+)-sclareolide. Bioorganic & Medicinal Chemistry Letters. 16(6). 1656–1659. 34 indexed citations
14.
Oh, Sangtae, In Howa Jeong, Chan Mug Ahn, Woon‐Seob Shin, & Seokjoon Lee. (2004). Synthesis and antiangiogenic activity of thioacetal artemisinin derivatives. Bioorganic & Medicinal Chemistry. 12(14). 3783–3790. 42 indexed citations
15.
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
16.
Oh, Sangtae, In Howa Jeong, & Seokjoon Lee. (2004). Efficient Synthesis ofexo-Olefinated Deoxoartemisinin Derivatives by Ramberg−Bäcklund Rearrangement. The Journal of Organic Chemistry. 69(3). 984–986. 5 indexed citations
17.
Oh, Sangtae, et al.. (2003). A study on the synthesis of antiangiogenic (+)-coronarin A and congeners from (+)-sclareolide. Bioorganic & Medicinal Chemistry Letters. 13(12). 2009–2012. 11 indexed citations
18.
Oh, Sangtae, In Howa Jeong, Woon‐Seob Shin, & Seokjoon Lee. (2003). Growth inhibition activity of thioacetal artemisinin derivatives against human umbilical vein endothelial cells. Bioorganic & Medicinal Chemistry Letters. 13(21). 3665–3668. 29 indexed citations
19.
Lee, Seokjoon & Sangtae Oh. (2002). A simple synthesis of C-10 substituted deoxoartemisinin and 9-epi-deoxoartemisinin with various organozinc reagents. Tetrahedron Letters. 43(16). 2891–2894. 13 indexed citations
20.
Wheeler, J. W., et al.. (1972). Cyclopentanoid norsesquiterpenes from gyrinid beetles. Journal of the American Chemical Society. 94(21). 7589–7590. 12 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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