Hao Jiang

4.8k total citations · 2 hit papers
77 papers, 4.1k citations indexed

About

Hao Jiang is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Hao Jiang has authored 77 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Organic Chemistry, 15 papers in Inorganic Chemistry and 12 papers in Molecular Biology. Recurrent topics in Hao Jiang's work include Asymmetric Synthesis and Catalysis (26 papers), Synthetic Organic Chemistry Methods (16 papers) and Synthesis and Catalytic Reactions (13 papers). Hao Jiang is often cited by papers focused on Asymmetric Synthesis and Catalysis (26 papers), Synthetic Organic Chemistry Methods (16 papers) and Synthesis and Catalytic Reactions (13 papers). Hao Jiang collaborates with scholars based in Denmark, China and Sweden. Hao Jiang's co-authors include Karl Anker Jørgensen, Łukasz Albrecht, Kim L. Jensen, Gustav Dickmeiss, Björn Gschwend, Márcio W. Paixão, Petteri Elsner, David Monge, Rebecca L. Davis and Aurelia Falcicchio and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Hao Jiang

72 papers receiving 4.1k citations

Hit Papers

The Diarylprolinol Silyl Ether System: A General Organoca... 2011 2026 2016 2021 2011 2023 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hao Jiang Denmark 32 3.7k 782 620 205 166 77 4.1k
Fangrui Zhong China 33 3.9k 1.1× 1.1k 1.4× 818 1.3× 262 1.3× 84 0.5× 92 4.2k
Hideo Togo Japan 39 5.2k 1.4× 765 1.0× 882 1.4× 279 1.4× 234 1.4× 249 5.5k
Steven W. M. Crossley United States 11 1.8k 0.5× 528 0.7× 443 0.7× 158 0.8× 154 0.9× 12 2.4k
Carlos Roque D. Correia Brazil 36 3.5k 0.9× 528 0.7× 638 1.0× 117 0.6× 216 1.3× 161 4.1k
Corinna S. Schindler United States 32 2.7k 0.7× 456 0.6× 633 1.0× 133 0.6× 185 1.1× 84 3.0k
Govindasamy Sekar India 41 4.3k 1.1× 884 1.1× 630 1.0× 122 0.6× 333 2.0× 152 4.6k
Hong‐Gang Cheng China 34 3.1k 0.8× 627 0.8× 275 0.4× 166 0.8× 236 1.4× 81 3.5k
Chun‐An Fan China 37 4.4k 1.2× 739 0.9× 564 0.9× 195 1.0× 150 0.9× 104 4.7k
Osamu Onomura Japan 34 3.0k 0.8× 826 1.1× 876 1.4× 187 0.9× 122 0.7× 141 3.4k
Sherry R. Chemler United States 45 5.9k 1.6× 1.3k 1.7× 648 1.0× 301 1.5× 161 1.0× 89 6.4k

Countries citing papers authored by Hao Jiang

Since Specialization
Citations

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

Fields of papers citing papers by Hao Jiang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hao Jiang

This figure shows the co-authorship network connecting the top 25 collaborators of Hao Jiang. A scholar is included among the top collaborators of Hao Jiang 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 Hao Jiang. Hao Jiang 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.
Zhang, Xiaojing, Hao Jiang, Yaqin Li, et al.. (2025). RLCKs phosphorylate RopGEFs to control auxin-dependent Arabidopsis development. Nature Plants. 11(10). 2130–2144.
2.
Jiang, Hao & Ulf Ryde. (2024). Putative reaction mechanism of nitrogenase with a half-dissociated S2B ligand. Dalton Transactions. 53(27). 11500–11513. 2 indexed citations
3.
Jiang, Hao, et al.. (2024). Tuning lanthanide luminescence from bipyridine-bis(oxazoline/thiazoline) tetradentate ligands. Chinese Journal of Structural Chemistry. 43(9). 100354–100354. 3 indexed citations
5.
Jiang, Hao & Ulf Ryde. (2023). H2 formation from the E2–E4 states of nitrogenase. Physical Chemistry Chemical Physics. 26(2). 1364–1375. 2 indexed citations
6.
Jiang, Hao, et al.. (2023). Visible-Light-Driven Zinc Oxide Quantum Dots for the Management of Bacterial Fruit Blotch Disease and the Improvement of Melon Seedlings Growth. Journal of Agricultural and Food Chemistry. 71(6). 2773–2783. 16 indexed citations
7.
Vysotskiy, Victor P., Hao Jiang, Ernst D. Larsson, et al.. (2023). Assessment of DFT functionals for a minimal nitrogenase [Fe(SH)4H]− model employing state-of-the-art ab initio methods. The Journal of Chemical Physics. 159(4). 6 indexed citations
9.
Chen, Qian, et al.. (2019). Nitration–Peroxidation of Alkenes: A Selective Approach to β-Peroxyl Nitroalkanes. Organic Letters. 21(5). 1480–1483. 51 indexed citations
10.
Monge, David, Hao Jiang, & Yolanda Álvarez‐Casao. (2015). Masked Unsaturated Esters/Amides in Asymmetric Organocatalysis. Chemistry - A European Journal. 21(12). 4494–4504. 40 indexed citations
11.
Davis, Rebecca L., Julian Stiller, Tricia Naicker, Hao Jiang, & Karl Anker Jørgensen. (2014). Asymmetric Organocatalytic Epoxidations: Reactions, Scope, Mechanisms, and Applications. Angewandte Chemie International Edition. 53(29). 7406–7426. 118 indexed citations
12.
Li, Yang, et al.. (2014). Trienamine-mediated asymmetric [4+2]-cycloaddition of α,β-unsaturated ester surrogates applying 4-nitro-5-styrylisoxazoles. Chemical Communications. 50(99). 15689–15691. 34 indexed citations
13.
Stiller, Julian, Dorota Kowalczyk, Hao Jiang, Karl Anker Jørgensen, & Łukasz Albrecht. (2014). Novel Organocatalytic Activation of Unmodified Morita–Baylis–Hillman Alcohols for the Synthesis of Bicyclic α‐Alkylidene‐Ketones. Chemistry - A European Journal. 20(41). 13108–13112. 26 indexed citations
14.
Jiang, Hao, Lennart Lykke, Steen Uttrup Pedersen, Wen‐Jing Xiao, & Karl Anker Jørgensen. (2012). A practical electromediated ipso-hydroxylation of aryl and alkyl boronic acids under an air atmosphere. Chemical Communications. 48(57). 7203–7203. 45 indexed citations
15.
Jiang, Hao, et al.. (2009). Achieving Molecular Complexity by Organocatalytic One‐Pot Strategies—A Fast Entry for Synthesis of Sphingoids, Amino Sugars, and Polyhydroxylated α‐Amino Acids. Angewandte Chemie International Edition. 48(37). 6844–6848. 108 indexed citations
16.
Jiang, Hao, et al.. (2009). Iminium‐Ion Activation as an Efficient Strategy for Divergent Synthesis of Optically Active Propargylic, Homopropargylic, and Allenic Compounds. Chemistry - A European Journal. 15(38). 9638–9641. 19 indexed citations
17.
Jiang, Hao, Peng Xia, & Qian Zhang. (2008). 4-(7-Acetoxy-6-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)phenyl acetate. Acta Crystallographica Section E Structure Reports Online. 64(7). o1230–o1230. 1 indexed citations
18.
Reyes, Efraím, et al.. (2007). How to Make Five Contiguous Stereocenters in One Reaction: Asymmetric Organocatalytic Synthesis of Pentasubstituted Cyclohexanes. Angewandte Chemie International Edition. 46(48). 9202–9205. 117 indexed citations
19.
Zou, Cheng, et al.. (1999). Structures of rubiarbonone B and C. Acta Botanica Yunnanica. 21(2). 256–259. 3 indexed citations
20.
Sakakibara, Iwao, Susumu Terabayashi, Masayoshi Kubo, et al.. (1998). Effect of oxindole alkaloids from the hooks of Uncaria macrophylla on thiopental-induced hypnosis. Phytomedicine. 5(2). 83–86. 33 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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