Shohei Sase

678 total citations
37 papers, 560 citations indexed

About

Shohei Sase is a scholar working on Organic Chemistry, Inorganic Chemistry and Toxicology. According to data from OpenAlex, Shohei Sase has authored 37 papers receiving a total of 560 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Organic Chemistry, 15 papers in Inorganic Chemistry and 13 papers in Toxicology. Recurrent topics in Shohei Sase's work include Organoselenium and organotellurium chemistry (13 papers), Synthesis and characterization of novel inorganic/organometallic compounds (9 papers) and Sulfur-Based Synthesis Techniques (8 papers). Shohei Sase is often cited by papers focused on Organoselenium and organotellurium chemistry (13 papers), Synthesis and characterization of novel inorganic/organometallic compounds (9 papers) and Sulfur-Based Synthesis Techniques (8 papers). Shohei Sase collaborates with scholars based in Japan, Germany and Spain. Shohei Sase's co-authors include Kei Goto, Paul Knochel, Takayuki Kawashima, Albrecht Metzger, Vladimir Malakhov, Milica Jaric, Ryosuke Masuda, Keiichi Shimada, Naokazu Kano and Pradipta Sinha and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Shohei Sase

34 papers receiving 557 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shohei Sase Japan 13 415 124 118 82 66 37 560
Keiichi Shimada Japan 10 161 0.4× 58 0.5× 100 0.8× 86 1.0× 30 0.5× 17 316
Lihao Liao China 15 648 1.6× 138 1.1× 237 2.0× 52 0.6× 25 0.4× 27 756
Bhagat Singh Bhakuni India 10 691 1.7× 57 0.5× 280 2.4× 52 0.6× 29 0.4× 12 752
Ehrenfried Bulka Germany 11 460 1.1× 42 0.3× 201 1.7× 106 1.3× 26 0.4× 67 512
Fabrı́cio Vargas Brazil 15 586 1.4× 167 1.3× 308 2.6× 90 1.1× 28 0.4× 20 649
Márcio S. Silva Brazil 17 666 1.6× 80 0.6× 375 3.2× 73 0.9× 19 0.3× 66 777
Satoru Kuwano Japan 14 656 1.6× 206 1.7× 35 0.3× 123 1.5× 18 0.3× 38 732
Alexander Breder Germany 18 1.1k 2.6× 160 1.3× 398 3.4× 84 1.0× 25 0.4× 35 1.2k
Senthil Narayanaperumal Brazil 13 352 0.8× 54 0.4× 169 1.4× 44 0.5× 17 0.3× 16 390
Diana M. Freudendahl United Kingdom 6 597 1.4× 99 0.8× 485 4.1× 12 0.1× 32 0.5× 8 646

Countries citing papers authored by Shohei Sase

Since Specialization
Citations

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

Fields of papers citing papers by Shohei Sase

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shohei Sase

This figure shows the co-authorship network connecting the top 25 collaborators of Shohei Sase. A scholar is included among the top collaborators of Shohei Sase 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 Shohei Sase. Shohei Sase 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.
2.
Kuwano, Satoru, et al.. (2022). Oxy- and aminoselenation of alkenes utilizing an isolable selenenyl iodide. Mendeleev Communications. 32(1). 80–82. 3 indexed citations
3.
Masuda, Ryosuke, et al.. (2021). Modeling the Catalytic Cycle of Glutathione Peroxidase by Nuclear Magnetic Resonance Spectroscopic Analysis of Selenocysteine Selenenic Acids. Journal of the American Chemical Society. 143(17). 6345–6350. 47 indexed citations
4.
Masuda, Ryosuke, et al.. (2021). Isolable small-molecule cysteine sulfenic acid. Chemical Communications. 57(20). 2479–2482. 18 indexed citations
5.
Sase, Shohei, et al.. (2019). Model study on trapping of protein selenenic acids by utilizing a stable synthetic congener. New Journal of Chemistry. 43(18). 6830–6833. 11 indexed citations
6.
Shimada, Keiichi, et al.. (2016). Modeling of the Bioactivation of an Organic Nitrate by a Thiol to Form a Thionitrate Intermediate. Molecules. 22(1). 19–19. 5 indexed citations
7.
Sase, Shohei, et al.. (2015). Synthesis, Structure, and Reactivities of a Stable Primary-alkyl-substituted Sulfenic Acid. Chemistry Letters. 44(5). 615–617. 13 indexed citations
8.
Domoto, Yuya, Shohei Sase, & Kei Goto. (2014). Efficient End‐Capping Synthesis of Neutral Donor–Acceptor [2]Rotaxanes Under Additive‐Free and Mild Conditions. Chemistry - A European Journal. 20(48). 15998–16005. 8 indexed citations
9.
10.
Sase, Shohei, et al.. (2014). Synthesis of a Stable Selenoaldehyde by Self‐Catalyzed Thermal Dehydration of a Primary‐Alkyl‐Substituted Selenenic Acid. Angewandte Chemie International Edition. 54(3). 901–904. 20 indexed citations
11.
Sase, Shohei, et al.. (2014). Synthesis of a Stable Selenoaldehyde by Self‐Catalyzed Thermal Dehydration of a Primary‐Alkyl‐Substituted Selenenic Acid. Angewandte Chemie. 127(3). 915–918. 1 indexed citations
12.
Sasamori, Takahiro, et al.. (2011). Formation of a Unique Fluorosilene–KF Complex Bearing Bulky Substituents. Chemistry Letters. 40(2). 196–197. 3 indexed citations
13.
Domoto, Yuya, et al.. (2010). Synthesis and Properties of Pentacoordinated Phenoxysilane and Carboxysilanes with Intramolecular Nitrogen–Silicon Coordination. Phosphorus, sulfur, and silicon and the related elements. 185(5-6). 1221–1229. 1 indexed citations
14.
Domoto, Yuya, et al.. (2010). Catalyst-Free Syntheses of [2]Rotaxanes Utilizing a Pentacoordinated Hydrosilane as an End-Capping Agent. Organic Letters. 12(11). 2586–2589. 13 indexed citations
15.
16.
Goto, Kei, et al.. (2009). Modeling of the 5′‐Deiodination of Thyroxine by Iodothyronine Deiodinase: Chemical Corroboration of a Selenenyl Iodide Intermediate. Angewandte Chemie International Edition. 49(3). 545–547. 53 indexed citations
17.
Sase, Shohei, Milica Jaric, Albrecht Metzger, Vladimir Malakhov, & Paul Knochel. (2008). One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates. The Journal of Organic Chemistry. 73(18). 7380–7382. 117 indexed citations
18.
Tsuji, Hayato, Tomoyuki Inoue, Shohei Sase, & Kohei Tamao. (2006). trans-Dichlorobis(10-dodecyl-9-phospha-10-silatriptycene-κP)palladium(II). Acta Crystallographica Section E Structure Reports Online. 62(3). m535–m537. 4 indexed citations
19.
Sase, Shohei, Naokazu Kano, & Takayuki Kawashima. (2004). Isolation of a Cyclic Intermediate in the Reaction of a Phosphorus Ylide with Elemental Sulfur: Synthesis, Structure, and Reactivity of a 1,2σ5-Thiaphosphirane. Chemistry Letters. 33(11). 1434–1435. 5 indexed citations
20.
Sase, Shohei, Naokazu Kano, & Takayuki Kawashima. (2002). Novel Synthetic Method of Fluorophosphoranes by Fluoride Ion Abstraction from Tetrafluoroborate. Phosphorus, sulfur, and silicon and the related elements. 177(8-9). 2041–2041. 1 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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