Qing‐Qing Kang

574 total citations
16 papers, 530 citations indexed

About

Qing‐Qing Kang is a scholar working on Organic Chemistry, Inorganic Chemistry and Astronomy and Astrophysics. According to data from OpenAlex, Qing‐Qing Kang has authored 16 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 4 papers in Inorganic Chemistry and 2 papers in Astronomy and Astrophysics. Recurrent topics in Qing‐Qing Kang's work include Catalytic C–H Functionalization Methods (10 papers), Sulfur-Based Synthesis Techniques (9 papers) and Radical Photochemical Reactions (6 papers). Qing‐Qing Kang is often cited by papers focused on Catalytic C–H Functionalization Methods (10 papers), Sulfur-Based Synthesis Techniques (9 papers) and Radical Photochemical Reactions (6 papers). Qing‐Qing Kang collaborates with scholars based in China, Australia and South Korea. Qing‐Qing Kang's co-authors include Wen‐Ting Wei, Qiang Li, La‐Sheng Long, Lan‐Sun Zheng, Rong‐Bin Huang, Wei‐Min He, Xiaoxiao Meng, Shu‐Ting Wu, Zhiping Zheng and Hui Zhang and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and Green Chemistry.

In The Last Decade

Qing‐Qing Kang

16 papers receiving 526 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Qing‐Qing Kang China	10	370	165	93	72	53	16	530
Błażej Dziuk Poland	14	335 0.9×	100 0.6×	114 1.2×	67 0.9×	33 0.6×	68	507
Ludovic Gremaud Switzerland	13	397 1.1×	160 1.0×	69 0.7×	33 0.5×	19 0.4×	25	499
Guo‐Xin Jin China	11	338 0.9×	248 1.5×	98 1.1×	148 2.1×	33 0.6×	15	458
Jin‐Ji Wu China	16	212 0.6×	256 1.6×	125 1.3×	121 1.7×	49 0.9×	18	446
Lynne Horsburgh United Kingdom	18	528 1.4×	327 2.0×	122 1.3×	42 0.6×	42 0.8×	36	639
Chris Gendy Canada	11	322 0.9×	191 1.2×	66 0.7×	35 0.5×	126 2.4×	23	446
Lucia M. Lee Canada	6	212 0.6×	103 0.6×	156 1.7×	64 0.9×	167 3.2×	6	421
Mónica Moya‐Cabrera Mexico	13	323 0.9×	251 1.5×	89 1.0×	49 0.7×	28 0.5×	41	420
S. Graule France	5	313 0.8×	125 0.8×	130 1.4×	39 0.5×	26 0.5×	5	353
Jian Fan China	14	465 1.3×	94 0.6×	65 0.7×	34 0.5×	28 0.5×	21	521

Countries citing papers authored by Qing‐Qing Kang

Since Specialization

Citations

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

Fields of papers citing papers by Qing‐Qing Kang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Qing‐Qing Kang. 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 Qing‐Qing Kang. The network helps show where Qing‐Qing Kang may publish in the future.

Co-authorship network of co-authors of Qing‐Qing Kang

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

All Works

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16 of 16 papers shown

1.

Kang, Qing‐Qing, et al.. (2022). Copper-catalyzed switchable cyclization of alkyne-tethered α-bromocarbonyls: selective access to quinolin-2-ones and quinoline-2,4-diones. Organic Chemistry Frontiers. 9(23). 6617–6623. 14 indexed citations

2.

Wang, Dongkai, Qing‐Qing Kang, Guo‐Ping Ge, et al.. (2021). Sulfonyl radical triggered selective iodosulfonylation and bicyclization of 1,6-dienes. Chemical Communications. 57(67). 8288–8291. 22 indexed citations

3.

Liu, Hongxin, Wen‐Ting Wei, Qing‐Qing Kang, et al.. (2021). Radical Cyclization of Olefinic Amides through α-C(sp3)–H Functionalization of Ketones under Catalyst-, Ligand-, and Base-Free Conditions. Synlett. 32(9). 905–912. 5 indexed citations

4.

Kang, Qing‐Qing, Yanan Meng, Guo‐Ping Ge, et al.. (2021). Iron-catalyzed oxidative cyclization of olefinic 1,3-dicarbonyls with ketone C(sp³)–H bonds: facile access to 2,3-dihydrofurans. New Journal of Chemistry. 45(30). 13639–13643. 7 indexed citations

5.

Kang, Qing‐Qing, Yi Liu, Guo‐Ping Ge, et al.. (2021). Selective divergent radical cyclization of 1,6-dienes with alkyl nitriles. Organic & Biomolecular Chemistry. 19(43). 9501–9505. 6 indexed citations

6.

Kang, Qing‐Qing, Weikang Zhang, Guo‐Ping Ge, Hongxing Zheng, & Wen‐Ting Wei. (2021). The construction of benzimidazo[2,1-a]isoquinolin-6(5H)-ones from N-methacryloyl-2-phenylbenzoimidazoles through radical strategies. Organic & Biomolecular Chemistry. 19(41). 8874–8885. 18 indexed citations

7.

Kang, Qing‐Qing, Wenfeng Wu, Qiang Li, & Wen‐Ting Wei. (2020). Photochemical strategies for C–N bond formation via metal catalyst-free (hetero) aryl C(sp²)–H functionalization. Green Chemistry. 22(10). 3060–3068. 57 indexed citations

8.

Cao, Tingting, Weikang Zhang, Qing‐Qing Kang, et al.. (2020). Halocyclization of Olefinic 1,3-Dicarbonyls and Olefinic Amides in Aqueous Media Open in Air at Room Temperature. ACS Sustainable Chemistry & Engineering. 8(45). 16946–16951. 18 indexed citations

9.

Meng, Xiaoxiao, et al.. (2020). Visible-light-initiated regioselective sulfonylation/cyclization of 1,6-enynes under photocatalyst- and additive-free conditions. Green Chemistry. 22(4). 1388–1392. 135 indexed citations

10.

Meng, Yanan, Qing‐Qing Kang, Tingting Cao, et al.. (2019). Oxone-Mediated Radical Bicyclization of 1,6-Enynes through Dual α-C(sp³)–H Functionalization of Ketones under Catalyst- and Base-Free Conditions. ACS Sustainable Chemistry & Engineering. 7(22). 18738–18743. 39 indexed citations

11.

Kang, Qing‐Qing, et al.. (2019). Selective Cyanoalkylation and [2+2+2] Annulation of 1,6‐Enynes with Azobis(alkylcarbonitriles) under Mild Conditions. European Journal of Organic Chemistry. 2019(47). 7673–7677. 12 indexed citations

12.

Kang, Qing‐Qing, et al.. (2019). Cu(NO ₃ ) ₂ /Oxone‐Mediated Radical Nitration Cyclization of 1,6‐Enynes. ChemistrySelect. 4(45). 13380–13383. 5 indexed citations

13.

Wu, Shu‐Ting, Qing‐Qing Kang, Hui Zhang, et al.. (2007). Chiral Symmetry Breaking by Chemically Manipulating Statistical Fluctuation in Crystallization. Angewandte Chemie International Edition. 46(44). 8475–8479. 170 indexed citations

14.

Wu, Shu‐Ting, Qing‐Qing Kang, Hui Zhang, et al.. (2007). Chiral Symmetry Breaking by Chemically Manipulating Statistical Fluctuation in Crystallization. Angewandte Chemie. 119(44). 8627–8631. 13 indexed citations

15.

Kang, Qing‐Qing, La‐Sheng Long, Rong‐Bin Huang, & Lan‐Sun Zheng. (2004). La(NO₂)₃, a novel (3,9)-connected lanthanide-based network. Acta Crystallographica Section E Structure Reports Online. 60(2). i12–i14. 5 indexed citations

16.

Kang, Qing‐Qing, La‐Sheng Long, Rong‐Bin Huang, & Lan‐Sun Zheng. (2004). Polymeric bis(glycolato)nickel(II). Acta Crystallographica Section E Structure Reports Online. 60(4). m406–m407. 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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