Deju Shang

1.2k total citations
19 papers, 1.0k citations indexed

About

Deju Shang is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Deju Shang has authored 19 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Organic Chemistry, 9 papers in Inorganic Chemistry and 4 papers in Molecular Biology. Recurrent topics in Deju Shang's work include Asymmetric Synthesis and Catalysis (9 papers), Asymmetric Hydrogenation and Catalysis (9 papers) and Sulfur-Based Synthesis Techniques (5 papers). Deju Shang is often cited by papers focused on Asymmetric Synthesis and Catalysis (9 papers), Asymmetric Hydrogenation and Catalysis (9 papers) and Sulfur-Based Synthesis Techniques (5 papers). Deju Shang collaborates with scholars based in China, United States and United Kingdom. Deju Shang's co-authors include Xiaoming Feng, Xiaohua Liu, Xin Zhou, Yanling Liu, Junguo Xin, P. Andrew Evans, Lili Lin, Lu Chang, Xu Yang and Mu‐Hyun Baik 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

Deju Shang

19 papers receiving 1.0k citations

Peers

Deju Shang
Masayuki Hoshi Japan
Noël Collignon France
George Y. Li United States
Tue B. Petersen Denmark
Robert Naasz Netherlands
R. Soundararajan India
Changmin Xie China
Jun Yong Kang United States
Haruka Shimizu Japan
Mark S. Kerr United States
Masayuki Hoshi Japan
Deju Shang
Citations per year, relative to Deju Shang Deju Shang (= 1×) peers Masayuki Hoshi

Countries citing papers authored by Deju Shang

Since Specialization
Citations

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

Fields of papers citing papers by Deju Shang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deju Shang

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

All Works

19 of 19 papers shown
1.
Huang, Rong, et al.. (2024). Total Synthesis of Stachybotrys microspora Triprenol Phenol-7 (SMTP-7). Organic Letters. 26(3). 697–701. 2 indexed citations
2.
Li, Chaomin, Shujun Wang, Jianxin Yang, et al.. (2023). From Chiral Resolution to Diastereoselective Ellman Chemistry to Biocatalysis: Route Evolution for the Efficient Synthesis of the Tetrahydrobenzoazepine Core of BTK Inhibitor BIIB091. Organic Process Research & Development. 27(8). 1463–1473. 2 indexed citations
3.
Li, Chaomin, Fredrik Hæffner, Shujun Wang, et al.. (2021). Sulfone Displacement Approach for Large-Scale Synthesis of 4-Chloro-N-(1-methyl-1H-pyrazol-4-yl)pyrimidin-2-amine. Organic Process Research & Development. 26(1). 137–143. 5 indexed citations
4.
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Mazumder, Shivnath, et al.. (2012). Stereoselective Rhodium-Catalyzed [3 + 2 + 1] Carbocyclization of Alkenylidenecyclopropanes with Carbon Monoxide: Theoretical Evidence for a Trimethylenemethane Metallacycle Intermediate. Journal of the American Chemical Society. 134(51). 20569–20572. 99 indexed citations
7.
Liu, Yanling, Deju Shang, Xin Zhou, Xiaohua Liu, & Xiaoming Feng. (2009). Enantioselective Friedel–Crafts Alkylation of Indoles with Alkylidene Malonates Catalyzed by N,N′‐Dioxide–Scandium(III) Complexes: Asymmetric Synthesis of β‐Carbolines. Chemistry - A European Journal. 15(9). 2055–2058. 112 indexed citations
8.
Shang, Deju, Yanling Liu, Xin Zhou, Xiaohua Liu, & Xiaoming Feng. (2009). A N,N′‐Dioxide–Copper(II) Complex as an Efficient Catalyst for the Enantioselective and Diastereoselective Mannich‐Type Reaction of Glycine Schiff Bases with Aldimines. Chemistry - A European Journal. 15(15). 3678–3681. 63 indexed citations
9.
Zhou, Xin, Yanling Liu, Lu Chang, et al.. (2009). Highly Efficient Synthesis of Quaternary α‐Hydroxy Phosphonates via Lewis Acid‐Catalyzed Hydrophosphonylation of Ketones. Advanced Synthesis & Catalysis. 351(16). 2567–2572. 60 indexed citations
10.
Zhou, Xin, Deju Shang, Qi Zhang, et al.. (2009). Enantioselective Three-Component Kabachnik−Fields Reaction Catalyzed by Chiral Scandium(III)−N,N′-Dioxide Complexes. Organic Letters. 11(6). 1401–1404. 56 indexed citations
11.
Liu, Yanling, Deju Shang, Xin Zhou, et al.. (2009). AgAsF6/Sm(OTf)3 Promoted Reversal of Enantioselectivity for the Asymmetric Friedel−Crafts Alkylations of Indoles with β,γ-Unsaturated α-Ketoesters. Organic Letters. 12(1). 180–183. 87 indexed citations
12.
Liu, Yanling, Xin Zhou, Deju Shang, Xiaohua Liu, & Xiaoming Feng. (2009). N,N′-Dioxide–scandium(III) complex catalyzed highly enantioselective Friedel–Crafts alkylation of indole to alkylidene malonates. Tetrahedron. 66(7). 1447–1457. 26 indexed citations
13.
Chen, Xiaohong, Jun Wang, Yin Zhu, et al.. (2008). A Secondary Amine Amide Organocatalyst for the Asymmetric Nitroaldol Reaction of α‐Ketophosphonates. Chemistry - A European Journal. 14(35). 10896–10899. 48 indexed citations
14.
Xin, Junguo, Lu Chang, Zongrui Hou, et al.. (2008). An Enantioselective Biginelli Reaction Catalyzed by a Simple Chiral Secondary Amine and Achiral Brønsted Acid by a Dual‐Activation Route. Chemistry - A European Journal. 14(10). 3177–3181. 99 indexed citations
15.
Chang, Lu, Deju Shang, Junguo Xin, Xiaohua Liu, & Xiaoming Feng. (2008). Chiral N,N′-dioxide-iron(II) complexes catalyzed enantioselective oxa-Michael addition of α,β-unsaturated aldehydes. Tetrahedron Letters. 49(47). 6663–6666. 17 indexed citations
16.
Zhou, Xin, Xiaohua Liu, Xu Yang, et al.. (2007). Highly Enantioselective Hydrophosphonylation of Aldehydes Catalyzed by Tridentate Schiff Base Aluminum(III) Complexes. Angewandte Chemie International Edition. 47(2). 392–394. 108 indexed citations
17.
Zhou, Xin, Xiaohua Liu, Xu Yang, et al.. (2007). Highly Enantioselective Hydrophosphonylation of Aldehydes Catalyzed by Tridentate Schiff Base Aluminum(III) Complexes. Angewandte Chemie. 120(2). 398–400. 39 indexed citations
18.
Shang, Deju, Junguo Xin, Yanling Liu, et al.. (2007). Enantioselective Aza-Diels−Alder Reaction of Aldimines with “Danishefsky-Type Diene” Catalyzed by Chiral Scandium(III)-N,N‘-Dioxide Complexes. The Journal of Organic Chemistry. 73(2). 630–637. 76 indexed citations
19.
Yang, Weiqing, Deju Shang, Yanling Liu, Ying Du, & Xiaoming Feng. (2005). Highly Enantioselective Synthesis of 2,6-Disubstituted and 2,2,6-Trisubstituted Dihydropyrones:  A One-Step Synthesis of (R)-(+)-Hepialone and Its Analogues. The Journal of Organic Chemistry. 70(21). 8533–8537. 44 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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