Chao‐Shan Da

1.7k total citations
58 papers, 1.4k citations indexed

About

Chao‐Shan Da is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Chao‐Shan Da has authored 58 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Organic Chemistry, 23 papers in Inorganic Chemistry and 16 papers in Molecular Biology. Recurrent topics in Chao‐Shan Da's work include Asymmetric Synthesis and Catalysis (44 papers), Asymmetric Hydrogenation and Catalysis (23 papers) and Synthetic Organic Chemistry Methods (16 papers). Chao‐Shan Da is often cited by papers focused on Asymmetric Synthesis and Catalysis (44 papers), Asymmetric Hydrogenation and Catalysis (23 papers) and Synthetic Organic Chemistry Methods (16 papers). Chao‐Shan Da collaborates with scholars based in China, Hong Kong and Bulgaria. Chao‐Shan Da's co-authors include Rui Wang, Zhaoqing Xu, Wenjin Yan, Albert S. C. Chan, Qipeng Guo, Daxue Liu, Xiaowu Yang, Xinyuan Fan, Jiangke Xu and Chao Chen and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

Chao‐Shan Da

56 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chao‐Shan Da China 22 1.3k 527 328 80 75 58 1.4k
Mathieu P. Lalonde United States 7 1.1k 0.8× 367 0.7× 404 1.2× 77 1.0× 70 0.9× 8 1.2k
Jérôme Blanchet France 22 1.2k 0.9× 350 0.7× 503 1.5× 63 0.8× 53 0.7× 46 1.4k
Pankaj Jain United States 13 1.5k 1.1× 429 0.8× 170 0.5× 65 0.8× 49 0.7× 16 1.5k
Chuchi Tang China 25 1.7k 1.3× 458 0.9× 384 1.2× 105 1.3× 48 0.6× 77 1.8k
Jean‐Nicolas Desrosiers United States 21 1.2k 0.9× 514 1.0× 302 0.9× 67 0.8× 98 1.3× 43 1.3k
Yongda Zhang United States 22 1.7k 1.3× 497 0.9× 363 1.1× 100 1.3× 133 1.8× 50 1.8k
Vijay N. Wakchaure Germany 20 1.2k 0.9× 562 1.1× 275 0.8× 61 0.8× 48 0.6× 26 1.3k
Carmen Concellón Spain 20 1.1k 0.9× 240 0.5× 285 0.9× 69 0.9× 84 1.1× 57 1.2k
Silvia Vera Spain 21 1.8k 1.4× 493 0.9× 358 1.1× 70 0.9× 50 0.7× 27 1.9k
Kohsuke Ohmatsu Japan 23 1.7k 1.3× 589 1.1× 301 0.9× 79 1.0× 78 1.0× 56 1.8k

Countries citing papers authored by Chao‐Shan Da

Since Specialization
Citations

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

Fields of papers citing papers by Chao‐Shan Da

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chao‐Shan Da. 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 Chao‐Shan Da. The network helps show where Chao‐Shan Da may publish in the future.

Co-authorship network of co-authors of Chao‐Shan Da

This figure shows the co-authorship network connecting the top 25 collaborators of Chao‐Shan Da. A scholar is included among the top collaborators of Chao‐Shan Da 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 Chao‐Shan Da. Chao‐Shan Da 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.
Zhao, Pengfei, Jing Wen, Zhengwang Zhu, et al.. (2025). Recent advances in chiral phosphoric acids for asymmetric organocatalysis: a catalyst design perspective. Organic & Biomolecular Chemistry. 23(35). 7872–7913. 1 indexed citations
2.
Yuan, Meng, et al.. (2021). Organocatalyzed Highly Enantioselective Aldol Reaction of Aldehydes for Synthesis of (R)‐Pantolactone. Asian Journal of Organic Chemistry. 10(5). 1167–1172. 5 indexed citations
3.
Yuan, Meng, et al.. (2020). N-Primary-amine tetrapeptide-catalyzed highly asymmetric Michael addition of aliphatic aldehydes to maleimides. Organic & Biomolecular Chemistry. 18(35). 6899–6904. 13 indexed citations
4.
Han, Zhi‐Jian, Weiping Li, Chao‐Shan Da, et al.. (2020). Ruthenium‐Catalyzed Double C(sp2)−H Functionalizations of Fumaramides with Alkynes for the Divergent Synthesis of Pyridones and Naphthyridinediones. ChemCatChem. 12(9). 2538–2547. 12 indexed citations
5.
Wang, Pei, et al.. (2017). Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones. Organic Letters. 19(10). 2634–2637. 49 indexed citations
6.
Li, Xiao, Lei Zhang, Qipeng Guo, et al.. (2016). Direct asymmetric aldol reaction of acetophenones with aromatic aldehydes catalyzed by chiral Al/Zn heterobimetallic compounds. Russian Journal of General Chemistry. 86(8). 1922–1930. 3 indexed citations
7.
Yuan, Rui, Dan Zhao, Xiang Pan, et al.. (2015). Isopropylmagnesium chloride-promoted unilateral addition of Grignard reagents to β-diketones: one-pot syntheses of β-tertiary hydroxyl ketones or 3-substituted cyclic-2-enones. Organic & Biomolecular Chemistry. 14(2). 724–728. 11 indexed citations
8.
9.
Zhang, Jiadi, Corneliu Stanciu, Beibei Wang, et al.. (2011). Palladium-Catalyzed Allylic Substitution with (η6-Arene–CH2Z)Cr(CO)3-Based Nucleophiles. Journal of the American Chemical Society. 133(50). 20552–20560. 93 indexed citations
10.
Fan, Xinyuan, et al.. (2010). AlCl3 and BDMAEE: A Pair of Potent Reactive Regulators of Aryl Grignard Reagents and Highly Catalytic Asymmetric Arylation of Aldehydes. Chemistry - A European Journal. 16(27). 7988–7991. 45 indexed citations
11.
12.
Ma, Xiao, et al.. (2009). Highly efficient prolinamide-based organocatalysts for the direct asymmetric aldol reaction in brine. Tetrahedron Letters. 50(25). 3059–3062. 44 indexed citations
13.
Da, Chao‐Shan, Junrui Wang, Xiaogang Yin, et al.. (2009). Highly Catalytic Asymmetric Addition of Deactivated Alkyl Grignard Reagents to Aldehydes. Organic Letters. 11(24). 5578–5581. 48 indexed citations
14.
Da, Chao‐Shan, et al.. (2009). N-Primary-Amine-Terminal β-Turn Tetrapeptides as Organocatalysts for Highly Enantioselective Aldol Reaction. The Journal of Organic Chemistry. 74(13). 4812–4818. 49 indexed citations
15.
Li, Hong, et al.. (2008). Direct Asymmetric Aldol Reaction of Aryl Ketones with Aryl Aldehydes Catalyzed by Chiral BINOL-Derived Zincate Catalyst. The Journal of Organic Chemistry. 73(18). 7398–7401. 28 indexed citations
16.
Han, Zhi‐Jian, et al.. (2005). The asymmetric addition of phenylacetylene to aldehydes catalyzed by l-leucine derived chiral sulfonamide alcohol ligands. Journal of Molecular Catalysis A Chemical. 236(1-2). 32–37. 7 indexed citations
17.
Xu, Zhaoqing, Rui Wang, Jiangke Xu, et al.. (2003). Highly Enantioselective Addition of Phenylacetylene to Aldehydes Catalyzed by a β‐Sulfonamide Alcohol–Titanium Complex. Angewandte Chemie International Edition. 42(46). 5747–5749. 112 indexed citations
18.
19.
Liu, Daxue, Quan Wang, Chao‐Shan Da, et al.. (2001). The Application of Chiral Aminonaphthols in the Enantioselective Addition of Diethylzinc to Aryl Aldehydes. Organic Letters. 3(17). 2733–2735. 100 indexed citations
20.
Yang, Xiaowu, Jianheng Shen, Chao‐Shan Da, et al.. (2001). Highly enantioselective addition of diethylzinc to aldehydes catalyzed by a new chiral C2-symmetric Ti–diol complex. Tetrahedron Letters. 42(37). 6573–6575. 21 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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