Jia‐Di Huang
About
Jia‐Di Huang is a scholar working on Organic Chemistry, Inorganic Chemistry and Biomedical Engineering.
According to data from OpenAlex, Jia‐Di Huang has authored 29 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Organic Chemistry, 21 papers in Inorganic Chemistry and 10 papers in Biomedical Engineering. Recurrent topics in Jia‐Di Huang's work include Asymmetric Hydrogenation and Catalysis (20 papers), Asymmetric Synthesis and Catalysis (11 papers) and Surface Chemistry and Catalysis (10 papers). Jia‐Di Huang is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (20 papers), Asymmetric Synthesis and Catalysis (11 papers) and Surface Chemistry and Catalysis (10 papers). Jia‐Di Huang collaborates with scholars based in China and Japan. Jia‐Di Huang's co-authors include Xiang‐Ping Hu, Zhuo Zheng, Daoyong Wang, Sai‐Bo Yu, Zheng‐Chao Duan, Jun Deng, Ken‐ichi Tominaga, Xuefeng Xu, Jun Deng and Min Qiu and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and ACS Catalysis.
In The Last Decade
Jia‐Di Huang
29 papers receiving 697 citations
Peers
Jia‐Di Huang
Micaela Toniutti Italy
Zheng‐Chao Duan China
Dibyajyoti Panja India
Jannik C. Borghs Germany
Sutthichat Kerdphon Sweden
Jian‐Bo Xie China
Qingqing Bu China
Weilong Wu China
Santo Magnolia Italy
Lavinia Panella Netherlands
Citations per year, relative to Jia‐Di Huang Jia‐Di Huang (= 1×)
peers
Micaela Toniutti
Countries citing papers authored by Jia‐Di Huang
Since
Specialization
Citations
This map shows the geographic impact of Jia‐Di 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 Jia‐Di Huang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jia‐Di Huang more than expected).
Fields of papers citing papers by Jia‐Di Huang
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Jia‐Di 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 Jia‐Di Huang. The network helps show where Jia‐Di Huang may publish in the future.
Co-authorship network of co-authors of Jia‐Di Huang
This figure shows the co-authorship network connecting the top 25 collaborators of Jia‐Di Huang. A scholar is included among the top collaborators of Jia‐Di 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 Jia‐Di Huang. Jia‐Di Huang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Han, Mei‐Ling, Xiang‐Ping Hu, Jia‐Di Huang, Ligong Chen, & Zhuo Zheng. (2011). New chiral amino alcohol ligands derived from 1-phenylethylamine for efficient Ru-catalyzed asymmetric transfer hydrogenation. Tetrahedron Asymmetry. 22(2). 222–225.
2.
Zhou, Xiaomao, et al.. (2010). Chiral 1-phenylethylamine-derived phosphine-phosphoramidite ligands for highly enantioselective Rh-catalyzed hydrogenation of β-(acylamino)acrylates: significant effect of substituents on 3,3′-positions of binaphthyl moiety. Organic & Biomolecular Chemistry. 8(10). 2320–2320.
3.
Zhou, Xiaomao, et al.. (2010). Readily available chiral phosphine–aminophosphine ligands derived from 1-phenylethylamine for Rh-catalyzed enantioselective hydrogenations. Tetrahedron Asymmetry. 21(4). 420–424.
4.
Qiu, Min, Daoyong Wang, Xiang‐Ping Hu, et al.. (2009). Asymmetric synthesis of chiral Roche ester and its derivatives via Rh-catalyzed enantioselective hydrogenation with chiral phosphine-phosphoramidite ligands. Tetrahedron Asymmetry. 20(2). 210–213.
5.
Yu, Sai‐Bo, Jia‐Di Huang, Daoyong Wang, et al.. (2008). Novel chiral phosphine-phosphoramidite ligands derived from 1-naphthylamine for highly efficient Rh-catalyzed asymmetric hydrogenation. Tetrahedron Asymmetry. 19(15). 1862–1866.
6.
Duan, Zheng‐Chao, Xiang‐Ping Hu, Daoyong Wang, et al.. (2008). Enantioselective Synthesis of Optically Active Alkanephos‐ phonates via Rhodium‐Catalyzed Asymmetric Hydrogenation of β‐Substituted α,β‐Unsaturated Phosphonates with Ferrocene‐Based Monophosphoramidite Ligands. Advanced Synthesis & Catalysis. 350(13). 1979–1983.
7.
Deng, Jun, Xiang‐Ping Hu, Jia‐Di Huang, et al.. (2008). Enantioselective Synthesis of β2-Amino Acids via Rh-Catalyzed Asymmetric Hydrogenation with BoPhoz-Type Ligands: Important Influence of an N−H Proton in the Ligand on the Enantioselectivity. The Journal of Organic Chemistry. 73(5). 2015–2017.
8.
Duan, Zheng‐Chao, Jia‐Di Huang, Xiang‐Ping Hu, et al.. (2008). Rh-Catalyzed Asymmetric Hydrogenation of γ-Phthalimido-Substituted α,β-Unsaturated Carboxylic Acid Esters: An Efficient Enantioselective Synthesis of β-Aryl-γ-amino Acids. Organic Letters. 10(15). 3379–3379.
9.
Qiu, Min, Xiang‐Ping Hu, Jia‐Di Huang, et al.. (2008). Modular Phosphine‐Aminophosphine Ligands Based on Chiral 1,2,3,4‐Tetrahydro‐1‐naphthylamine Backbone: A New Class of Practical Ligands for Enantioselective Hydrogenations. Advanced Synthesis & Catalysis. 350(17). 2683–2689.
10.
Qiu, Min, Xiang‐Ping Hu, Daoyong Wang, et al.. (2008). Chiral 1,2,3,4‐Tetrahydro‐1‐naphthylamine‐Derived Phosphine‐Phosphoramidite Ligand (THNAPhos): Application in Highly Enantioselective Hydrogenations of Functionalized CC Bonds. Advanced Synthesis & Catalysis. 350(9). 1413–1418.
11.
Wang, Daoyong, Xiang‐Ping Hu, Jia‐Di Huang, et al.. (2007). Highly Enantioselective Synthesis of α‐Hydroxy Phosphonic Acid Derivatives by Rh‐Catalyzed Asymmetric Hydrogenation with Phosphine–Phosphoramidite Ligands. Angewandte Chemie International Edition. 46(41). 7810–7813.
12.
Huang, Jia‐Di, Xiang‐Ping Hu, Sai‐Bo Yu, et al.. (2007). Readily available phosphine–imine ligands from α-phenylethylamine for highly efficient Pd-catalyzed asymmetric allylic alkylation. Journal of Molecular Catalysis A Chemical. 270(1-2). 127–131.
13.
Deng, Jun, Zheng‐Chao Duan, Jia‐Di Huang, et al.. (2007). Rh-Catalyzed Asymmetric Hydrogenation of γ-Phthalimido-Substituted α,β-Unsaturated Carboxylic Acid Esters: An Efficient Enantioselective Synthesis of β-Aryl-γ-amino Acids. Organic Letters. 9(23). 4825–4828.
14.
Wang, Daoyong, Xiang‐Ping Hu, Jia‐Di Huang, et al.. (2007). Highly Enantioselective Synthesis of α‐Hydroxy Phosphonic Acid Derivatives by Rh‐Catalyzed Asymmetric Hydrogenation with Phosphine–Phosphoramidite Ligands. Angewandte Chemie. 119(41). 7956–7959.
15.
Huang, Jia‐Di, Xiang‐Ping Hu, Zheng‐Chao Duan, et al.. (2006). Readily Available Phosphine−Phosphoramidite Ligands for Highly Efficient Rh-Catalyzed Enantioselective Hydrogenations. Organic Letters. 8(19). 4367–4370.
16.
Hu, Xiang‐Ping, et al.. (2005). Readily available, recoverable and soluble polymer-monophosphite ligands for highly enantioselective Rh-catalyzed hydrogenation. Chemical Communications. 293–295.
17.
Cai, Mingzhong, Jia‐Di Huang, & Rongli Zhang. (2004). Stereoselective synthesis of (E)‐α‐aryltellurenylvinylstannanes and their application in the synthesis of stereodefined trisubstituted alkenes. Chinese Journal of Chemistry. 22(8). 859–862.
18.
Cai, Mingzhong & Jia‐Di Huang. (2004). Stereoselective Synthesis of (E)-α-Silylvinyl Tellurides via the Hydrozirconation Reaction of Alkynylsilanes. Journal of Chemical Research. 2004(3). 228–229.
19.
Cai, Mingzhong, Jia‐Di Huang, & Wenyan Hao. (2003). (E)‐α‐Bromovinylselenides as Convenient Precursors for Stereoselective Synthesis of Trisubstituted Alkenes. Chinese Journal of Chemistry. 21(11). 1491–1493.
20.
Cai, Mingzhong, Chun‐Yun Peng, Hong Zhao, & Jia‐Di Huang. (2002). Stereoselective Synthesis of 1,3-enynylselenides via Palladium-Catalysed Cross Coupling Reactions. Journal of Chemical Research. 2002(8). 376–377.
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