Hideaki Hioki

1.5k total citations
65 papers, 1.3k citations indexed

About

Hideaki Hioki is a scholar working on Molecular Biology, Organic Chemistry and Rehabilitation. According to data from OpenAlex, Hideaki Hioki has authored 65 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 36 papers in Organic Chemistry and 11 papers in Rehabilitation. Recurrent topics in Hideaki Hioki's work include Chemical Synthesis and Analysis (16 papers), Plant-derived Lignans Synthesis and Bioactivity (15 papers) and Magnolia and Illicium research (11 papers). Hideaki Hioki is often cited by papers focused on Chemical Synthesis and Analysis (16 papers), Plant-derived Lignans Synthesis and Bioactivity (15 papers) and Magnolia and Illicium research (11 papers). Hideaki Hioki collaborates with scholars based in Japan, China and United States. Hideaki Hioki's co-authors include Miwa Kubo, Yoshiyasu Fukuyama, Kenichi Harada, W. Clark Still, Shô Itô, Mitsuaki Kodama, Jianmei Huang, Wanxia Tang, Tomoyuki Esumi and Tetsuto Tsunoda and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Hideaki Hioki

63 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hideaki Hioki Japan 21 752 674 177 146 127 65 1.3k
Tomoyuki Esumi Japan 23 984 1.3× 538 0.8× 87 0.5× 54 0.4× 136 1.1× 52 1.4k
Miwa Kubo Japan 25 582 0.8× 870 1.3× 307 1.7× 47 0.3× 419 3.3× 100 1.7k
Yi‐Kang Si China 18 405 0.5× 437 0.6× 40 0.2× 51 0.3× 242 1.9× 32 1.0k
Edmundo A. Rúveda Argentina 22 640 0.9× 890 1.3× 26 0.1× 110 0.8× 348 2.7× 95 1.6k
Guy L. F. Lemière Belgium 25 1.5k 2.0× 1.1k 1.6× 16 0.1× 129 0.9× 170 1.3× 95 2.2k
Seisho Tobinaga Japan 18 650 0.9× 355 0.5× 23 0.1× 36 0.2× 178 1.4× 112 1.2k
Xinfu Pan China 24 1.3k 1.7× 536 0.8× 18 0.1× 55 0.4× 126 1.0× 129 1.8k
Hongbin Zhai China 33 3.0k 4.0× 593 0.9× 55 0.3× 35 0.2× 47 0.4× 172 3.4k
Yasushi Kawai Japan 28 934 1.2× 1.2k 1.8× 11 0.1× 352 2.4× 58 0.5× 109 2.1k
Miguel Cardá Spain 30 2.1k 2.7× 1.0k 1.5× 15 0.1× 88 0.6× 181 1.4× 155 2.8k

Countries citing papers authored by Hideaki Hioki

Since Specialization
Citations

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

Fields of papers citing papers by Hideaki Hioki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hideaki Hioki

This figure shows the co-authorship network connecting the top 25 collaborators of Hideaki Hioki. A scholar is included among the top collaborators of Hideaki Hioki 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 Hideaki Hioki. Hideaki Hioki 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.
Harada, Kenichi, Kosho Makino, Tomoyuki Esumi, et al.. (2013). Total synthesis of riccardin C and (±)-cavicularin via Pd-catalyzed Ar–Ar cross couplings. Tetrahedron. 69(34). 6959–6968. 19 indexed citations
2.
Harada, Kenichi, Rich G. Carter, Tomoyuki Esumi, et al.. (2011). Asymmetric synthesis of (−)-chicanine using a highly regioselective intramolecular Mitsunobu reaction and revision of its absolute configuration. Tetrahedron Letters. 52(23). 3005–3008. 9 indexed citations
3.
Tang, Wanxia, Kenichi Harada, Miwa Kubo, Hideaki Hioki, & Yoshiyasu Fukuyama. (2011). Eight New Clerodane Diterpenoids from the Bark of Ptychopetalum olacoides. Natural Product Communications. 6(3). 327–32. 9 indexed citations
4.
Kubo, Miwa, et al.. (2010). NGF-potentiating vibsane-type diterpenoids from Viburnum sieboldii. Bioorganic & Medicinal Chemistry Letters. 20(8). 2566–2571. 34 indexed citations
5.
Yoshimoto, Mayumi, et al.. (2010). Novel Alkoxyamine Linker to Load Ketones for Solid-Phase Synthesis: Application of the Synthesis of 1,4-Benzodiazepine-2-ones. Journal of Combinatorial Chemistry. 12(3). 311–314. 6 indexed citations
6.
Hioki, Hideaki, et al.. (2009). Discovery of hydrolytic catalysts in a peptidocalixarene library by binding assay with a transition state analogue for the hydrolysis. Chemical Communications. 7194–7194. 2 indexed citations
7.
Hioki, Hideaki, Miwa Kubo, Tomoyuki Esumi, et al.. (2008). Synthesis of riccardin C and its seven analogues. Part 1: The role of their phenolic hydroxy groups as LXRα agonists. Bioorganic & Medicinal Chemistry Letters. 19(3). 738–741. 32 indexed citations
8.
Tang, Wanxia, Miwa Kubo, Kenichi Harada, Hideaki Hioki, & Yoshiyasu Fukuyama. (2008). Novel NGF-potentiating diterpenoids from a Brazilian medicinal plant, Ptychopetalum olacoides. Bioorganic & Medicinal Chemistry Letters. 19(3). 882–886. 27 indexed citations
9.
Tang, Wanxia, Hideaki Hioki, Kenichi Harada, Miwa Kubo, & Yoshiyasu Fukuyama. (2008). Clerodane Diterpenoids with NGF-Potentiating Activity from Ptychopetalum olacoides. Journal of Natural Products. 71(10). 1760–1763. 28 indexed citations
10.
Fukuyama, Yoshiyasu, Kenichi Harada, Tomoyuki Esumi, et al.. (2008). Synthesis of (—)-Talaumidin, a Neurotrophic 2,5-Biaryl-3,4-dimethyltetrahydrofuran Liganan, and Its Stereoisomers. Heterocycles. 76(1). 551–551. 14 indexed citations
11.
Hioki, Hideaki, A. Noda, Miwa Kubo, et al.. (2008). Total Synthesis of Pseudodehydrothyrsiferol. Organic Letters. 11(3). 579–582. 8 indexed citations
12.
Hioki, Hideaki, et al.. (2007). Solid-phase combinatorial synthesis of benzothiazoles, benzimidazoles, and benzoxazoles using a traceless linker. Tetrahedron. 63(46). 11315–11324. 24 indexed citations
13.
Kubo, Miwa, et al.. (2006). On-bead screening of a library to detect host–guest complexation by an aniline reporter. Chemical Communications. 3390–3392. 4 indexed citations
14.
Hioki, Hideaki, Hideki Takahashi, Miwa Kubo, et al.. (2005). Development of a new traceless aniline linker for solid-phase synthesis of azomethines. Application to parallel synthesis of a rod-shaped liquid crystalline library. Tetrahedron. 61(45). 10643–10651. 16 indexed citations
15.
Kodama, Mitsuaki, et al.. (2000). Asymmetric Total Synthesis of Terpenoids Possessing Novel Structure or Biological Activity.. Journal of Synthetic Organic Chemistry Japan. 58(12). 1167–1177.
16.
Hioki, Hideaki, et al.. (1998). Enantioselective Synthesis of Reported Hippospongic Acid A. Synlett. 1998(7). 729–730. 4 indexed citations
17.
Matsushita, Masayuki, et al.. (1996). A Simple Method for the Conversion of Primary Alcohols into Terminal Olefins. Chemistry Letters. 25(12). 1039–1040. 19 indexed citations
18.
Hioki, Hideaki, et al.. (1995). Intramolecular amidoalkylation of chiral imines and iminium ions: Stereoselective synthesis of anti-1,2- and -1,3-aminoalcohols. Tetrahedron Letters. 36(13). 2289–2292. 13 indexed citations
19.
Hioki, Hideaki, et al.. (1993). Intramolecular amidoalkylation of chiral iminium ions: Stereoselective synthesis of syn- 1,3-aminoalcohols. Tetrahedron Letters. 34(38). 6131–6134. 23 indexed citations
20.
Hirama, Masahiro, Hideaki Hioki, Shô Itô, & Chizuko Kabuto. (1988). Conjugate addition of internal nucleophile to chiral vinyl sulfoxides with stereogenic center at the allylic carbon. “intramolecular” double asymmetric induction. Tetrahedron Letters. 29(25). 3121–3124. 22 indexed citations

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