Shu‐Jiang Tu

16.0k total citations · 1 hit paper
497 papers, 14.0k citations indexed

About

Shu‐Jiang Tu is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Shu‐Jiang Tu has authored 497 papers receiving a total of 14.0k indexed citations (citations by other indexed papers that have themselves been cited), including 486 papers in Organic Chemistry, 78 papers in Molecular Biology and 70 papers in Pharmacology. Recurrent topics in Shu‐Jiang Tu's work include Multicomponent Synthesis of Heterocycles (277 papers), Synthesis and biological activity (149 papers) and Catalytic C–H Functionalization Methods (115 papers). Shu‐Jiang Tu is often cited by papers focused on Multicomponent Synthesis of Heterocycles (277 papers), Synthesis and biological activity (149 papers) and Catalytic C–H Functionalization Methods (115 papers). Shu‐Jiang Tu collaborates with scholars based in China, United States and Czechia. Shu‐Jiang Tu's co-authors include Bo Jiang, Wen‐Juan Hao, Guigen Li, Feng Shi, Xiang‐Shan Wang, Changsheng Yao, Shuliang Wang, Hao Wen, Walter J. Wever and Daqing Shi and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Shu‐Jiang Tu

482 papers receiving 13.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Multicomponent Reactions for the Synthesis of Heterocycles

2010 438 citations Bo Jiang, Shu‐Jiang Tu et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shu‐Jiang Tu China	63	13.6k	1.7k	1.1k	633	454	497	14.0k
Vijay Nair India	50	10.8k 0.8×	1.3k 0.7×	507 0.5×	1.0k 1.6×	334 0.7×	262	11.3k
Alakananda Hajra India	55	9.1k 0.7×	953 0.5×	297 0.3×	779 1.2×	557 1.2×	238	9.6k
Sandro Cacchi Italy	58	11.6k 0.9×	1.4k 0.8×	440 0.4×	1.5k 2.3×	412 0.9×	246	12.3k
Jie Wu China	76	20.8k 1.5×	1.8k 1.0×	474 0.5×	1.2k 1.9×	1.7k 3.7×	492	21.7k
Sambasivarao Kotha India	47	8.1k 0.6×	2.8k 1.6×	457 0.4×	594 0.9×	191 0.4×	371	8.8k
David J. Procter United Kingdom	63	10.8k 0.8×	1.4k 0.8×	310 0.3×	1.6k 2.5×	971 2.1×	230	12.1k
Issa Yavari Iran	41	7.1k 0.5×	912 0.5×	642 0.6×	304 0.5×	185 0.4×	594	7.8k
Giancarlo Fabrizi Italy	48	8.9k 0.7×	1.1k 0.6×	308 0.3×	1.1k 1.8×	311 0.7×	216	9.6k
Jie‐Ping Wan China	51	7.4k 0.5×	873 0.5×	514 0.5×	481 0.8×	595 1.3×	239	7.8k
Andrey P. Antonchick Germany	59	10.5k 0.8×	2.1k 1.2×	539 0.5×	2.8k 4.5×	511 1.1×	140	11.6k

Countries citing papers authored by Shu‐Jiang Tu

Since Specialization

Citations

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

Fields of papers citing papers by Shu‐Jiang Tu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shu‐Jiang Tu

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

All Works

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20 of 20 papers shown

Tu, Shu‐Jiang, et al.. (2024). Nanostructured NiCo2S4 immobilized on nickel foam as recyclable catalyst for activating peroxymonosulfate toward doxycycline degradation: Performance and mechanism. Separation and Purification Technology. 357. 129990–129990. 2 indexed citations

Wang, Jia‐Yin, Wen‐Juan Hao, Shu‐Jiang Tu, & Bo Jiang. (2022). Engaging Yne‐Allenes in Cycloaddition Reactions: Recent Developments. Chinese Journal of Chemistry. 40(10). 1224–1242. 37 indexed citations

Qin, Xiao‐Yan, et al.. (2021). Engaging yne-allenones in tunable catalytic silane-mediated conjugate transfer reductions. Chemical Communications. 57(44). 5394–5397. 16 indexed citations

Guo, Cheng, et al.. (2021). Cu-Catalyzed radical-triggered spirotricyclization of enediynes and enyne-nitriles for the synthesis of pentacyclic spiroindenes. Organic Chemistry Frontiers. 8(7). 1496–1502. 20 indexed citations

Zhang, Tian-Shu, et al.. (2021). Cyclic Oxime Esters as Deconstructive Bifunctional Reagents for Cyanoalkyl Esterification of 1,6-Enynes. The Journal of Organic Chemistry. 86(21). 15488–15497. 21 indexed citations

Chen, Yixin, et al.. (2021). Copper/silver co-mediated three-component bicyclization for accessing indeno[1,2-c]azepine-3,6-diones. Chemical Communications. 57(64). 7966–7969. 18 indexed citations

Hao, Wen‐Juan, et al.. (2020). Stereoselective synthesis of fully substituted ethylenes via an Ag-catalyzed 1,6-nucleophilic addition/annulation cascade. Chemical Communications. 56(56). 7749–7752. 11 indexed citations

Zhang, Tian-Shu, Hongping Zhang, Rong Fu, et al.. (2019). tert-Butyl peroxide (TBHP)/KI-mediated dual C(sp²)–H bond amination of arylamines with α-diazo carbonyls toward 1,2,4-benzotriazines. Chemical Communications. 55(88). 13231–13234. 20 indexed citations

Zhang, Tian-Shu, Rong Wang, Peijun Cai, et al.. (2019). Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides. Organic Chemistry Frontiers. 6(16). 2968–2973. 26 indexed citations

10.

Chen, Ke, Wen‐Juan Hao, Shu‐Jiang Tu, & Bo Jiang. (2019). Metal-free synthesis of triarylated (Z)-nitrones via H₂O-mediated 1,3-dipolar transfer under aerobic conditions. Green Chemistry. 21(3). 675–683. 33 indexed citations

11.

Shi, Haonan, Minhua Huang, Chun‐Lan He, et al.. (2019). Completely Stereoselective Synthesis of Sulfonated 1,3-Dihydroisobenzofurans via Radical Multicomponent Reactions. The Journal of Organic Chemistry. 84(21). 13686–13695. 33 indexed citations

12.

Wang, Jia‐Yin, Mengwei Li, Wen‐Juan Hao, et al.. (2018). N-Sulfonyl Bisimidazoline Ligands and Their Applications in Pd(II)-Catalyzed Asymmetric Addition toward α-Tertiary Amines. Organic Letters. 20(21). 6616–6621. 23 indexed citations

13.

Liu, Feng, et al.. (2018). Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols. Green Chemistry. 20(15). 3476–3485. 40 indexed citations

14.

Huang, Minhua, Wen‐Juan Hao, Guigen Li, Shu‐Jiang Tu, & Bo Jiang. (2018). Recent advances in radical transformations of internal alkynes. Chemical Communications. 54(77). 10791–10811. 190 indexed citations

15.

Zhu, Xiaotong, Xiang Wang, Tian-Shu Zhang, et al.. (2018). Substrate-Controlled Generation of 3-Sulfonylated 1-Indenones and 3-Arylated (Z)-Indenes via Cu-Catalyzed Radical Cyclization Cascades of o-Alkynylbenzonitriles. The Journal of Organic Chemistry. 83(17). 9890–9901. 45 indexed citations

16.

Li, Heng, Peng Zhou, Feng Xie, et al.. (2018). I₂-Mediated Iodobenzannulation of Yne-Allenones toward 1-Naphthols and Their Synthetic Application. The Journal of Organic Chemistry. 83(21). 13335–13343. 18 indexed citations

17.

Xu, Ting, et al.. (2018). Metal-free naphthannulation reactions of yne-allenone esters for accessing polycyclic aromatic hydrocarbons. Chemical Communications. 54(74). 10415–10418. 21 indexed citations

18.

Zhu, Xiaotong, Qi Zhao, Feng Liu, et al.. (2017). Silver-mediated radical 5-exo-dig cyclization of 2-alkynylbenzonitriles: synthesis of phosphinylated 1-indenones. Chemical Communications. 53(51). 6828–6831. 65 indexed citations

19.

Zhu, Yi‐Long, Ai‐Fang Wang, Jianyu Du, et al.. (2017). Ag-Catalyzed difluorohydration of β-alkynyl ketones for diastereoselective synthesis of 1,5-dicarbonyl compounds. Chemical Communications. 53(48). 6397–6400. 25 indexed citations

20.

Sun, Jun, Jiang‐Kai Qiu, Yanan Wu, et al.. (2017). Silver-Mediated Radical C(sp³)–H Biphosphinylation and Nitration of β-Alkynyl Ketones for Accessing Functional Isochromenes. Organic Letters. 19(4). 754–757. 74 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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