Qingmin Song

568 total citations · 1 hit paper
20 papers, 421 citations indexed

About

Qingmin Song is a scholar working on Organic Chemistry, Pharmaceutical Science and Inorganic Chemistry. According to data from OpenAlex, Qingmin Song has authored 20 papers receiving a total of 421 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 10 papers in Pharmaceutical Science and 3 papers in Inorganic Chemistry. Recurrent topics in Qingmin Song's work include Cyclopropane Reaction Mechanisms (17 papers), Catalytic C–H Functionalization Methods (14 papers) and Fluorine in Organic Chemistry (10 papers). Qingmin Song is often cited by papers focused on Cyclopropane Reaction Mechanisms (17 papers), Catalytic C–H Functionalization Methods (14 papers) and Fluorine in Organic Chemistry (10 papers). Qingmin Song collaborates with scholars based in China, Italy and Israel. Qingmin Song's co-authors include Xihe Bi, Paramasivam Sivaguru, Zhaohong Liu, Edward A. Anderson, Giuseppe Zanoni, Zikun Wang, Zhanjing Wang, Graham de Ruiter, Yongquan Ning and Xiaolong Zhang and has published in prestigious journals such as Angewandte Chemie International Edition, Nature Communications and Nature Chemistry.

In The Last Decade

Qingmin Song

19 papers receiving 420 citations

Hit Papers

Tunable molecular editing of indoles with fluoroalkyl car... 2024 2026 2025 2024 25 50 75

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Qingmin Song China 11 360 113 62 32 12 20 421
Chaosheng Luo United States 8 305 0.8× 116 1.0× 104 1.7× 59 1.8× 10 0.8× 10 364
Yuuki Maekawa Japan 12 583 1.6× 99 0.9× 114 1.8× 49 1.5× 21 1.8× 20 626
Benjamin T. Boyle United States 6 373 1.0× 71 0.6× 48 0.8× 32 1.0× 8 0.7× 6 403
Weizhi Geng China 11 474 1.3× 40 0.4× 81 1.3× 21 0.7× 30 2.5× 14 498
Shuya Yamada Japan 5 572 1.6× 49 0.4× 72 1.2× 28 0.9× 12 1.0× 7 586
Alan Wortman United States 6 393 1.1× 104 0.9× 53 0.9× 24 0.8× 14 1.2× 6 442
Ben Zhang China 6 316 0.9× 166 1.5× 79 1.3× 29 0.9× 7 0.6× 11 369
Ranjini Laskar Germany 7 301 0.8× 68 0.6× 37 0.6× 30 0.9× 9 0.8× 11 332
Florian W. Friese Germany 7 548 1.5× 77 0.7× 59 1.0× 43 1.3× 12 1.0× 7 573

Countries citing papers authored by Qingmin Song

Since Specialization
Citations

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

Fields of papers citing papers by Qingmin Song

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qingmin Song

This figure shows the co-authorship network connecting the top 25 collaborators of Qingmin Song. A scholar is included among the top collaborators of Qingmin Song 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 Qingmin Song. Qingmin Song 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.
Ning, Yongquan, et al.. (2026). Thermal [2+2] cycloaddition as a route to gem-difluoro heterobicyclo[n.1.1]alkanes. Nature Chemistry. 18(2). 283–293.
2.
Yang, Yong, Paramasivam Sivaguru, Qingmin Song, et al.. (2025). Copper‐Catalyzed Cyclopropenation of Alkynes with Difluoromethyl Carbene. Chinese Journal of Chemistry. 43(15). 1833–1840. 1 indexed citations
3.
Song, Qingmin, Paramasivam Sivaguru, Zhaohong Liu, et al.. (2024). Controllable Skeletal and Peripheral Editing of Pyrroles with Vinylcarbenes. Angewandte Chemie International Edition. 63(24). e202401359–e202401359. 21 indexed citations
4.
Zhang, Xiaolong, Qingmin Song, Paramasivam Sivaguru, et al.. (2024). Asymmetric dearomative single-atom skeletal editing of indoles and pyrroles. Nature Chemistry. 17(2). 215–225. 38 indexed citations
5.
Song, Qingmin, Zhaohong Liu, Paramasivam Sivaguru, et al.. (2024). Halogencarbene-free Ciamician-Dennstedt single-atom skeletal editing. Nature Communications. 15(1). 9998–9998. 28 indexed citations
6.
Song, Qingmin, et al.. (2024). Tunable molecular editing of indoles with fluoroalkyl carbenes. Nature Chemistry. 16(6). 988–997. 85 indexed citations breakdown →
7.
Song, Qingmin, Paramasivam Sivaguru, Zhaohong Liu, et al.. (2024). Controllable Skeletal and Peripheral Editing of Pyrroles with Vinylcarbenes. Angewandte Chemie. 136(24). 1 indexed citations
8.
Song, Qingmin, Yue Zhao, Shaopeng Liu, Yong Wu, & Zhaohong Liu. (2023). Stereoselective Synthesis of trans-Stilbenes through Silver-Catalyzed Self-Coupling of N-Triftosylhydrazones: An Experimental and Theoretical Study. Organic Letters. 25(19). 3461–3465. 4 indexed citations
9.
Zhang, Xiaolong, Yong Ji, Rong Li, et al.. (2023). Defluorinative 1,3‐Dienylation of Fluoroalkyl N‐Triftosylhydrazones with Homoallenols. Chemistry - A European Journal. 29(67). e202302562–e202302562. 5 indexed citations
10.
Wu, Yong, Qingmin Song, Ying Xia, et al.. (2023). Silver-catalyzed vinylcarbene insertion into Si–H bonds with vinyl N-triftosylhydrazones leading to allylsilanes. Organic Chemistry Frontiers. 10(18). 4588–4592. 4 indexed citations
12.
Yang, Yong, Zhaohong Liu, Qingmin Song, et al.. (2022). The merger of vinyl-N-triftosylhydrazones and silver catalysis to enable stereoselective vinylcyclopropanation of alkenes. Chem Catalysis. 2(3). 563–577. 25 indexed citations
13.
Ning, Yongquan, Qingmin Song, Paramasivam Sivaguru, et al.. (2022). Ag-Catalyzed Insertion of Alkynyl Carbenes into C–C Bonds of β-Ketocarbonyls: A Formal C(sp2) Insertion. Organic Letters. 24(2). 631–636. 30 indexed citations
14.
Liu, Zhaohong, Hongwei Wang, Paramasivam Sivaguru, et al.. (2022). Silver-catalyzed site-selective C(sp3)−H benzylation of ethers with N-triftosylhydrazones. Nature Communications. 13(1). 1674–1674. 41 indexed citations
15.
Liu, Zhaohong, Yong Yang, Qingmin Song, et al.. (2022). Chemoselective carbene insertion into the N−H bonds of NH3·H2O. Nature Communications. 13(1). 7649–7649. 34 indexed citations
17.
Song, Qingmin, Chengjie Feng, Zikun Wang, et al.. (2022). The Sulfinylsulfonation of alkynes for β‐Sulfinyl alkenylsulfone. Chemistry - An Asian Journal. 17(14). e202200299–e202200299. 20 indexed citations
18.
Zhang, Xiaolong, Xinyu Zhang, Qingmin Song, et al.. (2021). A Carbene Strategy for Progressive (Deutero)Hydrodefluorination of Fluoroalkyl Ketones. Angewandte Chemie. 134(7). 10 indexed citations
19.
Zhang, Xiaolong, Xinyu Zhang, Qingmin Song, et al.. (2021). A Carbene Strategy for Progressive (Deutero)Hydrodefluorination of Fluoroalkyl Ketones. Angewandte Chemie International Edition. 61(7). e202116190–e202116190. 44 indexed citations
20.
Liu, Binbin, Qingmin Song, Zhaohong Liu, & Zikun Wang. (2021). Silver‐Catalyzed Oxyphosphorylation of Unactivated Alkynes. Advanced Synthesis & Catalysis. 363(13). 3214–3219. 9 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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