Ke‐Yin Ye

4.0k total citations
103 papers, 3.4k citations indexed

About

Ke‐Yin Ye is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Ke‐Yin Ye has authored 103 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Organic Chemistry, 25 papers in Inorganic Chemistry and 19 papers in Pharmaceutical Science. Recurrent topics in Ke‐Yin Ye's work include Radical Photochemical Reactions (37 papers), Catalytic C–H Functionalization Methods (36 papers) and Sulfur-Based Synthesis Techniques (33 papers). Ke‐Yin Ye is often cited by papers focused on Radical Photochemical Reactions (37 papers), Catalytic C–H Functionalization Methods (36 papers) and Sulfur-Based Synthesis Techniques (33 papers). Ke‐Yin Ye collaborates with scholars based in China, Singapore and Germany. Ke‐Yin Ye's co-authors include Shu‐Li You, Yi Yu, Yaofeng Yuan, Song Lin, Li‐Xin Dai, Kai‐Jiong Xiao, Pei‐Qiang Huang, Chun‐Xiang Zhuo, Qing‐Feng Wu and Jie‐Min Luo and has published in prestigious journals such as Nature, Science and Journal of the American Chemical Society.

In The Last Decade

Ke‐Yin Ye

96 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ke‐Yin Ye China 32 3.1k 839 379 365 317 103 3.4k
Lin Guo China 37 3.6k 1.2× 652 0.8× 453 1.2× 386 1.1× 158 0.5× 108 3.8k
Manuel van Gemmeren Germany 29 2.3k 0.7× 761 0.9× 291 0.8× 198 0.5× 127 0.4× 70 2.6k
Corinne Gosmini France 37 4.0k 1.3× 761 0.9× 213 0.6× 328 0.9× 194 0.6× 102 4.3k
Lei Jiao China 37 4.2k 1.4× 851 1.0× 207 0.5× 318 0.9× 509 1.6× 84 4.9k
Wenbo Liu China 23 3.0k 1.0× 644 0.8× 513 1.4× 259 0.7× 141 0.4× 58 3.4k
Niankai Fu China 28 3.6k 1.1× 633 0.8× 407 1.1× 180 0.5× 644 2.0× 53 3.9k
Thomas Knauber United States 21 3.7k 1.2× 792 0.9× 491 1.3× 251 0.7× 153 0.5× 26 4.1k
Jin‐Tao Yu China 40 4.3k 1.4× 495 0.6× 494 1.3× 276 0.8× 154 0.5× 154 4.6k
Jacob T. Edwards United States 18 3.7k 1.2× 431 0.5× 447 1.2× 415 1.1× 224 0.7× 23 4.1k
João C. A. Oliveira Germany 35 3.1k 1.0× 865 1.0× 101 0.3× 168 0.5× 239 0.8× 75 3.4k

Countries citing papers authored by Ke‐Yin Ye

Since Specialization
Citations

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

Fields of papers citing papers by Ke‐Yin Ye

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ke‐Yin Ye. 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 Ke‐Yin Ye. The network helps show where Ke‐Yin Ye may publish in the future.

Co-authorship network of co-authors of Ke‐Yin Ye

This figure shows the co-authorship network connecting the top 25 collaborators of Ke‐Yin Ye. A scholar is included among the top collaborators of Ke‐Yin Ye 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 Ke‐Yin Ye. Ke‐Yin Ye 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.
Zhang, Ruiying, Lingyun Zhu, Yanxia Huang, et al.. (2025). Thiophene-backbone arcuate graphene nanoribbons: shotgun synthesis and length dependent properties. Chemical Science. 16(17). 7366–7373. 3 indexed citations
2.
Lin, Yuqi, Xiaomin Lin, Xinqi Xu, et al.. (2025). Synthesis of Chiral Sulfinamides Enabled by Polycyclic Ketone Monooxygenase Catalyzed Asymmetric Oxidation of Sulfenamides. ACS Catalysis. 15(18). 16247–16253. 1 indexed citations
3.
Zhang, Fengtao, et al.. (2025). Ligand‐Engineered Metal–Organic Frameworks of 3D Infinite Trinuclear Zinc Units for Photocatalytic Monooxygenation of Sulfenamides. Advanced Science. 12(33). e06037–e06037. 1 indexed citations
4.
Wang, Zhihua, et al.. (2025). One‐Pot, Divergent Synthesis of Sulfonimidoyl‐ and Sulfondiimidoyl Fluorides. Chinese Journal of Chemistry. 43(24). 3617–3622.
5.
Zhao, Bin, et al.. (2025). Electrochemical Conversions of Sulfinamidines into Sulfonimidoyl Fluorides. Organic Letters. 27(33). 9316–9321. 1 indexed citations
6.
Li, Minggang, Sha Yang, Cheng‐bin Gong, et al.. (2025). Electrophotocatalytic decarbonylative [4+2] cyclization of indenones. Chinese Chemical Letters. 37(6). 111709–111709. 1 indexed citations
7.
Hong, Yan, et al.. (2024). Porous electrocatalysts modified electrodes in organic electrocatalysis. Current Opinion in Electrochemistry. 45. 101478–101478. 6 indexed citations
8.
Wang, Zhihua, et al.. (2024). DMSO/SOCl2‐Mediated Synthesis of Thiomethylnaphthalenes from Propargyl Alcohols. Advanced Synthesis & Catalysis. 367(3). 3 indexed citations
9.
Zhao, Bin, et al.. (2024). Electrochemical Conversion of N‐Sulfinylamines to Sulfonimidoyl Fluorides. Chinese Journal of Chemistry. 43(7). 769–774. 5 indexed citations
10.
Shi, Zhaojiang, Shicheng Dong, Ting Liu, et al.. (2024). Electrochemical cascade migratory versus ortho -cyclization of 2-alkynylbenzenesulfonamides. Chemical Science. 15(8). 2827–2832. 10 indexed citations
11.
Guo, Peng, et al.. (2024). Cobalt-catalyzed migratory carbon-carbon cross-coupling of borabicyclo[3.3.1]nonane (9-BBN) borates. Chinese Chemical Letters. 36(4). 110052–110052.
12.
Chen, Lin, et al.. (2024). Cobalt‐Catalyzed Oxytrifluoromethylation of N‐Allylamides toward Trifluoromethyl‐Containing Oxazolines. Asian Journal of Organic Chemistry. 13(3).
13.
14.
Liu, Ting, Zhaojiang Shi, Yaofeng Yuan, Yuqi Lin, & Ke‐Yin Ye. (2023). Electrochemical Dearomative Spirocyclization of N‐Acyl Sulfonamides in a Continuous‐Flow Cell†. Chinese Journal of Chemistry. 42(9). 980–984. 6 indexed citations
15.
Liu, Ting, et al.. (2023). Electrochemical Selective Mono‐ and Polychlorination of Substituted Thiophenes. European Journal of Organic Chemistry. 27(1). 4 indexed citations
16.
17.
Ye, Ke‐Yin, Li‐Xin Dai, & Shu‐Li You. (2012). Enantioselective synthesis of 2,5-dihydrobenzo[b]azepine derivatives via iridium-catalyzed asymmetric allylic amination with 2-allylanilines and ring-closing-metathesis reaction. Organic & Biomolecular Chemistry. 10(30). 5932–5932. 33 indexed citations
18.
Wu, Qing‐Feng, Wen‐Bo Liu, Chun‐Xiang Zhuo, et al.. (2011). Iridium‐Catalyzed Intramolecular Asymmetric Allylic Dearomatization of Phenols. Angewandte Chemie International Edition. 50(19). 4455–4458. 270 indexed citations
19.
Xiao, Kai‐Jiong, Yu Wang, Ke‐Yin Ye, & Pei‐Qiang Huang. (2010). Versatile One‐Pot Reductive Alkylation of Lactams/Amides via Amide Activation: Application to the Concise Syntheses of Bioactive Alkaloids (±)‐Bgugaine, (±)‐Coniine, (+)‐Preussin, and (−)‐Cassine. Chemistry - A European Journal. 16(43). 12792–12796. 103 indexed citations
20.
Xiao, Kai‐Jiong, Jie‐Min Luo, Ke‐Yin Ye, Yu Wang, & Pei‐Qiang Huang. (2010). Direct, One‐pot Sequential Reductive Alkylation of Lactams/Amides with Grignard and Organolithium Reagents through Lactam/Amide Activation. Angewandte Chemie International Edition. 49(17). 3037–3040. 252 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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