Byung Tae Cho

1.7k total citations
52 papers, 1.3k citations indexed

About

Byung Tae Cho is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Byung Tae Cho has authored 52 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Organic Chemistry, 22 papers in Inorganic Chemistry and 18 papers in Molecular Biology. Recurrent topics in Byung Tae Cho's work include Asymmetric Synthesis and Catalysis (31 papers), Asymmetric Hydrogenation and Catalysis (22 papers) and Chemical Synthesis and Analysis (15 papers). Byung Tae Cho is often cited by papers focused on Asymmetric Synthesis and Catalysis (31 papers), Asymmetric Hydrogenation and Catalysis (22 papers) and Chemical Synthesis and Analysis (15 papers). Byung Tae Cho collaborates with scholars based in South Korea. Byung Tae Cho's co-authors include Yu Sung Chun, Herbert C. Brown, Dong Jun Kim, Namdu Kim, P. Veeraraghavan Ramachandran, Soo Ryeon Ryu, Nung Min Yoon, Min Sung Kim, Duk Keun An and Jahyo Kang and has published in prestigious journals such as Chemical Society Reviews, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Byung Tae Cho

51 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Byung Tae Cho South Korea 21 1.1k 606 460 142 104 52 1.3k
Jean‐Claude Fiaud France 25 1.3k 1.2× 661 1.1× 513 1.1× 182 1.3× 141 1.4× 69 1.6k
Katsuji Ito Japan 22 1.1k 1.0× 390 0.6× 229 0.5× 74 0.5× 80 0.8× 34 1.2k
David R. Schaad United States 5 1.6k 1.5× 549 0.9× 567 1.2× 93 0.7× 68 0.7× 7 1.8k
Toshiaki Morimoto Japan 25 1.2k 1.1× 900 1.5× 394 0.9× 75 0.5× 194 1.9× 76 1.4k
Sonia Rodrı́guez United States 20 1.2k 1.1× 520 0.9× 212 0.5× 105 0.7× 131 1.3× 47 1.4k
Jin Soon South Korea 17 600 0.6× 354 0.6× 274 0.6× 81 0.6× 92 0.9× 81 818
Gianni Palmieri Italy 23 1.7k 1.6× 278 0.5× 588 1.3× 160 1.1× 60 0.6× 63 1.9k
Michaela Edin Sweden 10 516 0.5× 496 0.8× 503 1.1× 139 1.0× 135 1.3× 14 843
T. TAKETOMI Japan 8 858 0.8× 657 1.1× 259 0.6× 115 0.8× 203 2.0× 17 1.1k
Bruce Z. Lu United States 23 1.5k 1.4× 523 0.9× 275 0.6× 75 0.5× 55 0.5× 34 1.6k

Countries citing papers authored by Byung Tae Cho

Since Specialization
Citations

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

Fields of papers citing papers by Byung Tae Cho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Byung Tae Cho. 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 Byung Tae Cho. The network helps show where Byung Tae Cho may publish in the future.

Co-authorship network of co-authors of Byung Tae Cho

This figure shows the co-authorship network connecting the top 25 collaborators of Byung Tae Cho. A scholar is included among the top collaborators of Byung Tae Cho 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 Byung Tae Cho. Byung Tae Cho 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.
Cho, Byung Tae. (2008). Recent development and improvement for boron hydride-based catalytic asymmetric reduction of unsymmetrical ketones. Chemical Society Reviews. 38(2). 443–452. 129 indexed citations
3.
Cho, Byung Tae. (2004). A Convenient Synthesis of Optically Active Unhindered Aliphatic Alcohols with High Optical Purity from Non-Racemic β-Hydroxy Sulfides. Bulletin of the Korean Chemical Society. 25(9). 1385–1391. 3 indexed citations
4.
Cho, Byung Tae, et al.. (2001). Synthesis of Optically Active 1,2-Indene Oxide and Vicinal cis-Aminoindanols via Asymmetric Reduction of 2-Tolylsulfonyloxy-1-indanone with (-)-B-Chlorodiisopinocampheylborane. Bulletin of the Korean Chemical Society. 22(11). 1261–1263. 2 indexed citations
5.
Cho, Byung Tae, et al.. (2001). Convenient synthesis of optically active 1,2-diol monosulfonates and terminal epoxides via oxazaborolidine-catalyzed asymmetric borane reduction of α-sulfonyloxy ketones. Journal of the Chemical Society Perkin Transactions 1. 1204–1211. 18 indexed citations
6.
Cho, Byung Tae, et al.. (2000). AN EFFICIENT SYNTHESIS OF ENANTIOPURE 3-CHLOROSTYRENE OXIDEviaOXAZABOROLIDINJGCATALYZED REDUCTION. Organic Preparations and Procedures International. 32(5). 493–497. 10 indexed citations
7.
Cho, Byung Tae & Yu Sung Chun. (1999). CATALYTIC ENANTIOSELCTIVE REACTIONS. PART 15. OXAZABOROLIDINE-CATALYZED ASYMMETRIC REDUCTION OF ALPHA -KETO ACETALS WITH N, N-DIETHYLANILINE-BORANE (D EANB) COMPLEX. Bulletin of the Korean Chemical Society. 20(4). 397–399. 4 indexed citations
8.
Cho, Byung Tae & Yu Sung Chun. (1999). Catalytic enantioselective reactions. Part 16. Oxazaborolidine-catalyzed asymmetric borane reduction of α-keto acetals. Journal of the Chemical Society Perkin Transactions 1. 2095–2100. 24 indexed citations
9.
Cho, Byung Tae & Yu Sung Chun. (1999). A practical method for synthesis of terminal 1,2-diols in high enantiomeric excess via oxazaborolidine-catalyzed asymmetric reduction. Tetrahedron Asymmetry. 10(10). 1843–1846. 32 indexed citations
10.
Kang, Jahyo, et al.. (1999). A concise synthesis of unnatural (+)-5-epi-nojirimycin-δ-lactam via asymmetric reduction of a meso-imide. Tetrahedron Asymmetry. 10(4). 657–660. 6 indexed citations
12.
Cho, Byung Tae & Yu Sung Chun. (1998). Facile Synthesis of Terminal 1,2-Diols with High Optical Purity via Oxazaborolidine-Catalyzed Asymmetric Borane Reduction. The Journal of Organic Chemistry. 63(15). 5280–5282. 31 indexed citations
14.
Cho, Byung Tae, et al.. (1994). Catalytic Enantioselective Reactions. Part 2.$^1$ A Comparison Study of Asymmetric Borane Reduction of Prochiral Ketones Catalyzed by Chiral Oxazaborolidines. Bulletin of the Korean Chemical Society. 15(2). 101–103. 1 indexed citations
15.
Cho, Byung Tae & Namdu Kim. (1994). Enantioselective addition of diethylzinc to aldehydes using γ-aminoalcohols derived from α-D-xylose as new chiral catalysts. Tetrahedron Letters. 35(24). 4115–4118. 25 indexed citations
17.
Cho, Byung Tae & Yu Sung Chun. (1992). Enantioselective synthesis of optically active metolachlor via asymmetric reduction. Tetrahedron Asymmetry. 3(3). 337–340. 14 indexed citations
18.
Brown, Herbert C., et al.. (1987). Selective reductions. 40. A critical examination of the relative effectiveness of various reducing agents for the asymmetric reduction of different classes of ketones. The Journal of Organic Chemistry. 52(24). 5406–5412. 75 indexed citations
19.
Brown, Herbert C., et al.. (1987). Addition compounds of alkali metal hydrides. 31. Preparation and properties of chiral dialkoxy monoalkylborohydrides. A new class of asymmetric reducing agents. The Journal of Organic Chemistry. 52(18). 4020–4024. 14 indexed citations
20.
Brown, Herbert C., et al.. (1986). Addition compounds of alkali metal hydrides. 29. Preparation and properties of chiral dialkylmonoalkoxyborohydrides. A new class of asymmetric reducing agents. The Journal of Organic Chemistry. 51(17). 3278–3282. 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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