Toshikazu Hakogi

477 citations

19 papers · 404 indexed · h-index 12

Organic Chemistry top 10%
- Carbohydrate Chemistry and Synthesis 8
- Synthetic Organic Chemistry Methods 3
- Synthesis and Catalytic Reactions 2
Pharmaceutical Science top 10%
Molecular Biology
- Sphingolipid Metabolism and Signaling 10
- Chemical Synthesis and Analysis 4
- Lipid Membrane Structure and Behavior 3
Biotechnology
- Marine Sponges and Natural Products 3
Cell Biology
Biomedical Engineering
- Innovative Microfluidic and Catalytic Techniques Innovation 3

Co-authors: Shigeo Katsumura Tetsuya Yamamoto Hiroko Hasegawa Shinobu Fujii Misako Taichi Kiyoshi Ikeda Toyoharu Kobayashi Katsunori Tanaka
Cited by: Organic Chemistry Pharmaceutical Science Molecular Biology
Journals: Chemical Communications (1 paper)The Journal of Organic Chemistry (2 papers)Industrial & Engineering Chemistry Research (1 paper)
Partner nations: Japan

In The Last Decade

Toshikazu Hakogi

19 papers receiving 400 citations

Peers

Countries citing papers authored by Toshikazu Hakogi

Since Specialization

Citations

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

Fields of papers citing papers by Toshikazu Hakogi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Toshikazu Hakogi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Toshikazu Hakogi Line = papers co-authored together Toshikazu Hakogi links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Kinetic Study and Model-Based Design Space Determination for a Drug Substance Flow Synthesis Using an Amination Reaction via Nucleophilic Aromatic Substitution Organic Process Research & Development ·Junu Kim,Yusuke Hayashi,Sara Badr,Kazuya Okamoto,Toshikazu Hakogi,Haruo Furukawa,Satoshi Yoshikawa,Hayao Nakanishi,Hirokazu Sugiyama	2024	2
2	Stereoselective Synthesis of Baloxavir Marboxil Using Diastereoselective Cyclization and Photoredox Decarboxylation of l-Serine The Journal of Organic Chemistry ·Kazuya Okamoto,Tatsuhiko Ueno,Yoshio Hato,Yasunori Kawaguchi,Toshikazu Hakogi,Shohei Majima,Takafumi Ohara,M. Hagihara,Norihiko Tánimoto,Takayuki Tsuritani	2024	3
3	Mechanistic insights into amination via nucleophilic aromatic substitution Reaction Chemistry & Engineering ·Junu Kim,Yusuke Hayashi,Sara Badr,Kazuya Okamoto,Toshikazu Hakogi,Haruo Furukawa,Satoshi Yoshikawa,Hayao Nakanishi,Hirokazu Sugiyama	2023	4
4	Hybrid Modeling of an Active Pharmaceutical Ingredient Flow Synthesis in a Ring-Opening Reaction of an Epoxide with a Grignard Reagent Industrial & Engineering Chemistry Research ·Junu Kim,Yusuke Hayashi,Sara Badr,Kazuya Okamoto,Toshikazu Hakogi,Haruo Furukawa,Satoshi Yoshikawa,Hayao Nakanishi,Hirokazu Sugiyama	2023	4
5	Practical and Scalable Synthetic Method for Preparation of Dolutegravir Sodium: Improvement of a Synthetic Route for Large-Scale Synthesis Organic Process Research & Development ·Yasunori Aoyama,Toshikazu Hakogi,Yuki Fukui,Daisuke Yamada,Takao Ooyama,Yutaka Nishino,Shoji Shinomoto,Masahiko Nagai,Naoki Miyake,Yoshiyuki Taoda,Hiroshi Yoshida,Tatsuro Yasukata	2019	16
6	Process Optimization of Aldol-Type Reaction by Process Understanding Using in Situ IR Organic Process Research & Development ·Yuki Fukui,Shinichi Oda,Hiroyuki Suzuki,Toshikazu Hakogi,Daisuke Yamada,Yohei Takagi,Yasunori Aoyama,Hideyuki Kitamura,Masayoshi Ogawa,Junko Kikuchi	2012	6
7	Syntheses of Fluorescence-labeled Sphingosine 1-Phosphate Methylene and Sulfur Analogues as Possible Visible Ligands to the Receptor Chemistry Letters ·Tetsuya Yamamoto,Hiroko Hasegawa,Toshikazu Hakogi,Shigeo Katsumura	2008	8
8	ChemInform Abstract: Syntheses of Fluorescence‐Labeled Sphingosine 1‐Phosphate Methylene and Sulfur Analogues as Possible Visible Ligands to the Receptor. ChemInform ·Tetsuya Yamamoto,Hiroko Hasegawa,Toshikazu Hakogi,Shigeo Katsumura	2008	1
9	Development of a One-Pot Asymmetric Azaelectrocyclization Protocol: Synthesis of Chiral 2,4-Disubstituted 1,2,5,6-Tetrahydropyridines Organic Letters ·Toyoharu Kobayashi,Miyuki Nakashima,Toshikazu Hakogi,Katsunori Tanaka,Shigeo Katsumura	2006	50
10	Versatile Synthetic Method for Sphingolipids and Functionalized Sphingosine Derivatives via Olefin Cross Metathesis Organic Letters ·Tetsuya Yamamoto,Hiroko Hasegawa,Toshikazu Hakogi,Shigeo Katsumura	2006	79
11	Synthesis of sphingomyelin difluoromethylene analogue Tetrahedron Letters ·Toshikazu Hakogi,Tetsuya Yamamoto,Shinobu Fujii,Kiyoshi Ikeda,Shigeo Katsumura	2006	30
12	Synthesis of sphingomyelin sulfur analogue and its behavior toward sphingomyelinase Bioorganic & Medicinal Chemistry Letters ·Toshikazu Hakogi,Shinobu Fujii,Michio Morita,Kiyoshi Ikeda,Shigeo Katsumura	2005	16
13	Useful Method for Direct Introduction of the Photoaffinity 3-(4-Hydroxyphenyl)-3-trifluoromethyldiazirine Group Chemistry Letters ·Toshihiko Shigenari,Toshikazu Hakogi,Shigeo Katsumura	2004	13
14	Cross Metathesis Route in Sphingomyelin Synthesis Chemistry Letters ·Hiroko Hasegawa,Tetsuya Yamamoto,Sho Hatano,Toshikazu Hakogi,Shigeo Katsumura	2004	18
15	Synthesis of fluorescence-Labeled sphingosine and sphingosine 1-phosphate; effective tools for sphingosine and sphingosine 1-phosphate behavior Bioorganic & Medicinal Chemistry Letters ·Toshikazu Hakogi,Toshihiko Shigenari,Shigeo Katsumura,Takamitsu Sano,Takayuki Kohno,Yasuyuki Igarashi	2003	25
16	Synthesis of a Nitrogen Analogue of Sphingomyelin as a Sphingomyelinase Inhibitor Organic Letters ·Toshikazu Hakogi,Misako Taichi,Shigeo Katsumura	2003	27
17	Synthesis of Sphingomyelin Carbon Analogues as Sphingomyelinase Inhibitors The Journal of Organic Chemistry ·Toshikazu Hakogi,Yoshiko Monden,Misako Taichi,Seiji Iwama,Shinobu Fujii,Kiyoshi Ikeda,Shigeo Katsumura	2002	37
18	Stereocontrolled Synthesis of a Sphingomyelin Methylene Analogue as a Sphingomyelinase Inhibitor Organic Letters ·Toshikazu Hakogi,Yoshiko Monden,Seiji Iwama,Shigeo Katsumura	2000	34
19	New entry for asymmetric deoxyazasugar synthesis: syntheses of deoxymannojirimycin, deoxyaltrojirimycin and deoxygalactostatin Chemical Communications ·Koji Asano,Toshikazu Hakogi,Seiji Iwama,Shigeo Katsumura	1999	31

About Toshikazu Hakogi

Toshikazu Hakogi is a scholar working on Organic Chemistry, Biotechnology and Molecular Biology, having authored 19 papers that have together received 404 indexed citations. Recurring topics across this work include Sphingolipid Metabolism and Signaling (10 papers), Carbohydrate Chemistry and Synthesis (8 papers), Chemical Synthesis and Analysis (4 papers), Innovative Microfluidic and Catalytic Techniques Innovation (3 papers), Marine Sponges and Natural Products (3 papers), Synthetic Organic Chemistry Methods (3 papers), Lipid Membrane Structure and Behavior (3 papers) and Synthesis and Catalytic Reactions (2 papers). The work is most often cited by research in Organic Chemistry (271 citations), Pharmaceutical Science (33 citations) and Molecular Biology (283 citations). Toshikazu Hakogi has collaborated with scholars based in Japan. Frequent co-authors include Shigeo Katsumura, Tetsuya Yamamoto, Hiroko Hasegawa, Shinobu Fujii, Misako Taichi, Kiyoshi Ikeda, Toyoharu Kobayashi, Katsunori Tanaka, Koji Asano and Takayuki Kohno. Their work appears in journals such as Chemical Communications, The Journal of Organic Chemistry and Industrial & Engineering Chemistry Research.

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