Miao Zhan

601 total citations
27 papers, 486 citations indexed

About

Miao Zhan is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Miao Zhan has authored 27 papers receiving a total of 486 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 5 papers in Molecular Biology and 5 papers in Pharmaceutical Science. Recurrent topics in Miao Zhan's work include Organoboron and organosilicon chemistry (8 papers), Catalytic Cross-Coupling Reactions (6 papers) and Catalytic C–H Functionalization Methods (5 papers). Miao Zhan is often cited by papers focused on Organoboron and organosilicon chemistry (8 papers), Catalytic Cross-Coupling Reactions (6 papers) and Catalytic C–H Functionalization Methods (5 papers). Miao Zhan collaborates with scholars based in China, Japan and United States. Miao Zhan's co-authors include Yuanwei Chen, Dawen Niu, Jie Liu, Ze‐Dong Mou, Chao-Guo Cao, Ren‐Zhe Li, Pengfei Li, Yuanwei Chen, Lifeng Zhao and Jiao Jiao and has published in prestigious journals such as Nature Communications, ACS Catalysis and Chemical Engineering Journal.

In The Last Decade

Miao Zhan

26 papers receiving 483 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miao Zhan China 14 288 124 100 86 65 27 486
Tao Fan China 16 834 2.9× 138 1.1× 61 0.6× 32 0.4× 42 0.6× 32 952
Thomas Wiesinger Austria 9 1.4k 4.7× 295 2.4× 139 1.4× 71 0.8× 240 3.7× 13 1.8k
Gaj Stavber Slovenia 15 469 1.6× 184 1.5× 76 0.8× 121 1.4× 42 0.6× 20 615
Shan‐Shan Zhu China 13 529 1.8× 56 0.5× 52 0.5× 60 0.7× 14 0.2× 23 648
Honghua Rao China 20 1.6k 5.6× 218 1.8× 172 1.7× 43 0.5× 20 0.3× 32 1.8k
David G. Cork Japan 14 306 1.1× 87 0.7× 97 1.0× 60 0.7× 13 0.2× 38 608
Guangyin Qian China 11 531 1.8× 80 0.6× 29 0.3× 24 0.3× 7 0.1× 12 597
Jia‐Jun Jiang China 13 607 2.1× 196 1.6× 92 0.9× 33 0.4× 47 0.7× 26 779
Katherine E. Jolley United Kingdom 12 221 0.8× 211 1.7× 148 1.5× 12 0.1× 19 0.3× 17 483

Countries citing papers authored by Miao Zhan

Since Specialization
Citations

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

Fields of papers citing papers by Miao Zhan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miao Zhan

This figure shows the co-authorship network connecting the top 25 collaborators of Miao Zhan. A scholar is included among the top collaborators of Miao Zhan 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 Miao Zhan. Miao Zhan 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.
2.
Xu, Liang, et al.. (2023). Iridium-catalyzed doubly stereoconvergent allylic alkylation of racemic α-boryl organozinc reagents. Chem Catalysis. 4(2). 100858–100858. 4 indexed citations
3.
4.
Feng, Chao, et al.. (2023). Access to Diverse Organoborons by α-Deprotonation and Functionalization of Benzylboronates. Organic Letters. 25(22). 4168–4172. 10 indexed citations
5.
Liu, Shaojun, Bo Zhang, Yingqiang Wu, et al.. (2022). Engineering manganese-rich phospho-olivine cathode materials with exposed crystal {0 1 0} facets for practical Li-ion batteries. Chemical Engineering Journal. 454. 139986–139986. 43 indexed citations
6.
Song, Xiaohui, Qiang Chang, Xuyong Feng, et al.. (2022). The regeneration of graphite anode from spent lithium-ion batteries by washing with a nitric acid/ethanol solution. New Carbon Materials. 37(5). 1011–1020. 20 indexed citations
7.
Zhan, Miao, et al.. (2021). Iridium-Catalyzed Enantioconvergent Allylation of a Boron-Stabilized Organozinc Reagent. The Journal of Organic Chemistry. 86(14). 9905–9913. 13 indexed citations
8.
Zhan, Miao, Zhengwei Ding, Haohua Chen, et al.. (2020). A unified approach for divergent synthesis of contiguous stereodiads employing a small boronyl group. Nature Communications. 11(1). 792–792. 19 indexed citations
9.
Wang, Fangying, Hongxia Jiang, Yu Jiang, et al.. (2018). Design, synthesis and biological evaluation of deuterated Vismodegib for improving pharmacokinetic properties. Bioorganic & Medicinal Chemistry Letters. 28(14). 2399–2402. 9 indexed citations
10.
Zhan, Miao, Xiang Pu, Bin He, Dawen Niu, & Xia Zhang. (2018). Intramolecular Umpolung Allylation of Imines. Organic Letters. 20(18). 5857–5860. 18 indexed citations
11.
Chen, Yutong, et al.. (2017). A Sensitive and Rapid Method for Detecting Formaldehyde in Brain Tissues. Analytical Cellular Pathology. 2017. 1–8. 6 indexed citations
12.
Tian, Ye, Shenzhen Huang, Miao Zhan, et al.. (2017). Synthesis and evaluation of novel thiazole‐based derivatives as selective inhibitors of DNA‐binding domain of the androgen receptor. Chemical Biology & Drug Design. 91(1). 172–180. 12 indexed citations
13.
Zhan, Miao, Ren‐Zhe Li, Ze‐Dong Mou, et al.. (2016). Silver-Assisted, Iridium-Catalyzed Allylation of Bis[(pinacolato)boryl]methane Allows the Synthesis of Enantioenriched Homoallylic Organoboronic Esters. ACS Catalysis. 6(5). 3381–3386. 114 indexed citations
14.
Zhan, Miao, Lingling Peng, Xuehai Pang, et al.. (2015). Design, synthesis and biological evaluation of deuterated nintedanib for improving pharmacokinetic properties. Journal of Labelled Compounds and Radiopharmaceuticals. 58(7). 308–312. 13 indexed citations
15.
Guo, Shiwei, Xuehai Pang, Lingling Peng, et al.. (2015). Design, synthesis and biological evaluation of deuterated Tivozanib for improving pharmacokinetic properties. Bioorganic & Medicinal Chemistry Letters. 25(11). 2425–2428. 21 indexed citations
16.
Zhan, Miao, Rui–Xue Xu, Ye Tian, et al.. (2015). A Simple and Cost‐Effective Method for the Regioselective Deuteration of Phenols. European Journal of Organic Chemistry. 2015(15). 3370–3373. 26 indexed citations
17.
Wu, Ting, Bing Hong, Xiaobing Wu, et al.. (2014). Persistent halogenated compounds in captive Chinese alligators (Alligator sinensis) from China. Chemosphere. 110. 23–30. 13 indexed citations
18.
Zhan, Miao, Tao Zhang, Haoxi Huang, Yongmei Xie, & Yuanwei Chen. (2014). A simple method for α‐position deuterated carbonyl compounds with pyrrolidine as catalyst. Journal of Labelled Compounds and Radiopharmaceuticals. 57(8). 533–539. 27 indexed citations
19.
Sun, Hongbao, Xiaoyan Wang, Miao Zhan, Jie Liu, & Yongmei Xie. (2013). Facile synthesis of novel tetrasubstituted 1-pyrazolines from Baylis–Hillman adducts and acyl diazomethanes. Tetrahedron Letters. 54(29). 3846–3850. 3 indexed citations
20.
Ji, Junfeng, et al.. (2010). Effect of flavones extract from Juglans mandshurica Maxim stem-barks on the p73-gene expression in hepatocarcinoma cell Bel-7402.. Shandong yiyao. 50(45). 10–12. 3 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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