Longjiang Huang

439 total citations
27 papers, 354 citations indexed

About

Longjiang Huang is a scholar working on Molecular Biology, Organic Chemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Longjiang Huang has authored 27 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Organic Chemistry and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Longjiang Huang's work include Chemical Synthesis and Analysis (8 papers), Phenothiazines and Benzothiazines Synthesis and Activities (6 papers) and Click Chemistry and Applications (4 papers). Longjiang Huang is often cited by papers focused on Chemical Synthesis and Analysis (8 papers), Phenothiazines and Benzothiazines Synthesis and Activities (6 papers) and Click Chemistry and Applications (4 papers). Longjiang Huang collaborates with scholars based in China, Bulgaria and Romania. Longjiang Huang's co-authors include Xiufen Li, Yu Han, Wei Dong, Qunqun Guo, Zhipeng Hou, Haibo Yu, Min Li, Jing Ding, Guorui Cao and Cheng Lian and has published in prestigious journals such as Journal of Medicinal Chemistry, Chemistry - A European Journal and British Journal of Pharmacology.

In The Last Decade

Longjiang Huang

27 papers receiving 345 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Longjiang Huang China 9 207 131 40 28 24 27 354
Anja Bodtke Germany 15 240 1.2× 190 1.5× 27 0.7× 62 2.2× 29 1.2× 38 469
Leszek Siergiejczyk Poland 11 112 0.5× 125 1.0× 37 0.9× 45 1.6× 38 1.6× 36 390
Mohammed Farrag El‐Behairy Egypt 12 212 1.0× 180 1.4× 92 2.3× 20 0.7× 8 0.3× 39 430
О. А. Нуркенов Kazakhstan 9 284 1.4× 92 0.7× 18 0.5× 23 0.8× 21 0.9× 111 362
Amol S. Kotmale India 14 288 1.4× 272 2.1× 48 1.2× 41 1.5× 12 0.5× 34 466
Luis A. Martínez Spain 15 171 0.8× 108 0.8× 29 0.7× 91 3.3× 17 0.7× 26 478
Maria Rosaria Del Giudice Italy 14 289 1.4× 153 1.2× 74 1.9× 19 0.7× 13 0.5× 39 464
Pawel Fludzinski United States 10 232 1.1× 165 1.3× 17 0.4× 18 0.6× 42 1.8× 15 423
Boris A. Czeskis United States 11 190 0.9× 90 0.7× 38 0.9× 11 0.4× 7 0.3× 35 328
И. В. Федорова Russia 12 231 1.1× 154 1.2× 16 0.4× 20 0.7× 66 2.8× 67 430

Countries citing papers authored by Longjiang Huang

Since Specialization
Citations

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

Fields of papers citing papers by Longjiang Huang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Longjiang Huang

This figure shows the co-authorship network connecting the top 25 collaborators of Longjiang Huang. A scholar is included among the top collaborators of Longjiang Huang 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 Longjiang Huang. Longjiang Huang 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.
Li, Fei, et al.. (2025). NaI‐Promoted Synthesis of Dihydroquinolines via an Unusual Azetine Intermediate. European Journal of Organic Chemistry. 28(13). 1 indexed citations
2.
Lou, Bin, et al.. (2025). Discovery of novel 4-azaindole derivatives as selective Nav1.2 Inhibitor with potent antiepileptic activity and low neurotoxicity. European Journal of Medicinal Chemistry. 292. 117664–117664. 1 indexed citations
3.
Wu, Jun, et al.. (2025). Design, synthesis and structure-activity relationship of novel 1,2,4-triazolopyrimidin-5-one derivatives targeting GABAA1 and Nav1.2 with antiepileptic activity. European Journal of Medicinal Chemistry. 286. 117316–117316. 3 indexed citations
4.
Zhang, Jingtao, et al.. (2024). The Potential of PARP Inhibitors as Antitumor Drugs and the Perspective of Molecular Design. Journal of Medicinal Chemistry. 68(1). 18–48. 6 indexed citations
5.
Li, Zhenpeng, et al.. (2024). A novel [1, 2, 4]triazolo[5,1-b]quinazoline derivative as a fluorescent probe for highly selective detection of Fe 3+ ions. Journal of Asian Natural Products Research. 26(2). 228–236. 2 indexed citations
6.
Wang, Rui, Yu Han, Xiufen Li, et al.. (2023). Design, synthesis, anticonvulsant activity and structure-activity relationships of novel 7-Azaindole derivatives. Bioorganic Chemistry. 133. 106430–106430. 10 indexed citations
7.
Zhang, Qin, Xintao Gao, Xiyu Duan, et al.. (2023). Design, synthesis and SAR of novel 7-azaindole derivatives as potential Erk5 kinase inhibitor with anticancer activity. Bioorganic & Medicinal Chemistry. 95. 117503–117503. 4 indexed citations
8.
9.
Lian, Cheng, et al.. (2022). Oxidative coupling of primary amines to imines catalyzed by CoCl2·6H2O. Applied Organometallic Chemistry. 36(3). 4 indexed citations
10.
Zhao, Fang, Shuangyan Wang, Yan Li, et al.. (2021). Surfactant cocamide monoethanolamide causes eye irritation by activating nociceptor TRPV1 channels. British Journal of Pharmacology. 178(17). 3448–3462. 12 indexed citations
11.
Wu, Jun, Zhipeng Hou, Yan Wang, et al.. (2021). Discovery of 7-alkyloxy- [1,2,4] triazolo[1,5-a] pyrimidine derivatives as selective positive modulators of GABAA1 and GABAA4 receptors with potent antiepileptic activity. Bioorganic Chemistry. 119. 105565–105565. 6 indexed citations
12.
Chen, Liping, Cheng Lian, Yu Han, et al.. (2021). A novel [1,2,4]triazolo[1,5-a]pyrimidine derivative as a fluorescence probe for specific detection of Fe3+ ions and application in cell imaging. Analytica Chimica Acta. 1187. 339168–339168. 33 indexed citations
13.
Han, Yu, Wei Dong, Qunqun Guo, Xiufen Li, & Longjiang Huang. (2020). The importance of indole and azaindole scaffold in the development of antitumor agents. European Journal of Medicinal Chemistry. 203. 112506–112506. 133 indexed citations
14.
Wang, Hui, et al.. (2020). Direct amidation of non‐activated carboxylic acid and amine derivatives catalyzed by TiCp2Cl2. Applied Organometallic Chemistry. 34(5). 8 indexed citations
15.
Lian, Cheng, et al.. (2020). Synthesis of the impurity F of salbutamol. Journal of Asian Natural Products Research. 22(10). 956–965. 1 indexed citations
16.
Huang, Longjiang, Jing Ding, Min Li, et al.. (2019). Discovery of [1,2,4]-triazolo [1,5-a]pyrimidine-7(4H)-one derivatives as positive modulators of GABAA1 receptor with potent anticonvulsant activity and low toxicity. European Journal of Medicinal Chemistry. 185. 111824–111824. 41 indexed citations
17.
Ge, Xiaoping, et al.. (2018). Direct amidation of non-activated phenylacetic acid and benzylamine derivatives catalysed by NiCl 2. Royal Society Open Science. 5(2). 171870–171870. 7 indexed citations
18.
Cao, Guorui, et al.. (2016). Synthetic Strategy and Anti-Tumor Activities of Macrocyclic Scaffolds Based on 4-Hydroxyproline. Molecules. 21(2). 212–212. 7 indexed citations
19.
Huang, Longjiang, et al.. (2009). The synthesis of analogs of shuangkangsu, a novel natural cycloperoxide glucoside fromLonicera japonicaThunb. Journal of Asian Natural Products Research. 11(2). 172–176. 1 indexed citations
20.
Yu, De‐Quan, et al.. (2008). The structure and absolute configuration of Shuangkangsu: a novel natural cyclic peroxide from Lonicera japonica (Thunb.). Journal of Asian Natural Products Research. 10(9). 851–856. 26 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Anja Bodtke Breakdown of academic impact, for papers by Leszek Siergiejczyk Breakdown of academic impact, for papers by Mohammed Farrag El‐Behairy Breakdown of academic impact, for papers by О. А. Нуркенов Breakdown of academic impact, for papers by Amol S. Kotmale Breakdown of academic impact, for papers by Luis A. Martínez Breakdown of academic impact, for papers by Maria Rosaria Del Giudice Breakdown of academic impact, for papers by Pawel Fludzinski Breakdown of academic impact, for papers by Boris A. Czeskis Breakdown of academic impact, for papers by И. В. Федорова
Rankless by CCL
2026