Publications

 2024   2023   2022   2021   2020   2019   2018

ORCiD      Google Scholar    2017以前の論文は左記を参照してください。

 2024

1.  Redox-Active Ligands: Concepts and Catalysis (Editor: Marine Desage-El Murr)

Part 2, Chapter 5, Redox-Active Ligands in Coordination Chemistry and Organic Synthesis 

Toru Amaya, Toshiyuki Moriuchi, Toshikazu Hirao, Wiley, January 2024.

Link

 2023

5.  Intramolecular Electron Transfer in Multi-Redox Systems Based on Cyclic [3]Spirobifluorenylene Compound

Tomoya Imai, Daisuke Sakamaki, Shinobu Aoyagi, and Toru Amaya*

Chem. Eur. J., 29 (70), e202302670 (2023).

https://doi.org/10.1002/chem.202302670


ChemRxiv (2023). (Preprint)

https://doi.org/10.26434/chemrxiv-2023-2kdbk-v3

4.  Synthesis and Host–Guest Chemistry of Chiral Spirobifluorene-Based Macrocycles Soluble in Basic Aqueous Solution

Kotoko Nakagawa, Kanaru Akimoto, Bunta Nakayasu, Saki Nagashima, Mamoru Tobisu, Michael P. Schramm, Shinobu Aoyagi, and Toru Amaya*

Org. Lett., 25 (32), 5969-5973 (2023).

https://doi.org/10.1021/acs.orglett.3c02074


Selected as a supplementary cover.

3.  Multiply exo-Methylated Corannulenes

Kazuhira Miwa, Shinobu Aoyagi,* Toru Amaya, Takahiro Sasamori,* Shogo Morisako, Takashi Kurogi, and Hideki Yorimitsu*

Chem. Eur. J., 29 (52), e202301557 (2023).

https://doi.org/10.1002/chem.202301557


Highlighted in ChemistryViews.

Selected as a front cover

2.  Synthesis of an Octacyclic C60 Fragment

Naruhiro Yoshida, Ryuhei Akasaka, Tomoya Imai, Michael P. Schramm, Yousuke Yamaoka, Toru Amaya, and Tetsuo Iwasawa* 

Eur. J. Org. Chem., 26 (33), e202300407 (2023).

https://doi.org/10.1002/ejoc.202300407


Highlighted in ChemistryViews.

1. エノラート種の酸化的クロスカップリング

雨夜 徹

化学と工業, 76 (1), 010 (2023).

リンク

 2022

.  Synthesis of Self-Doped Conductive Poly(3,4-ethylenedioxythiophene) (PEDOT) Bearing Phosphonic Acid Moieties

Kahori Kiriyama, Masato Daijo, Keiho Tsuchiya, Tomohiro Hatai, Toshikazu Hirao,* and Toru Amaya*

Bull. Chem. Soc. Jpn., 95 (8), 1228-1233 (2022).

https://doi.org/10.1246/bcsj.20220121

8.  Electrochemical and spectroscopic properties of twisted dibenzo[g,p]chrysene derivatives

Tomoya Imai, Ryuhei Akasaka, Naruhiro Yoshida, Toru Amaya*, and Tetsuo Iwasawa* 

Beilstein J. Org. Chem., 18, 963-971 (2022). (Open Access)

https://doi.org/10.3762/bjoc.18.96

7.  Message from Young Principal Researcher (MyPR)

有機化学の研究への誘い

雨夜 徹

有機合成化学協会誌, 80 (7), 693-695 (2022).

https://doi.org/10.5059/yukigoseikyokaishi.80.693

6.  ホウ素およびケイ素エノラート間の酸化的クロスカップリング

雨夜 徹*

有機合成化学協会誌, 80 (7), 654-663 (2022).

https://doi.org/10.5059/yukigoseikyokaishi.80.654

5.  Transformations of Main-Group Organometallics Induced by Transition Metals

Toshikazu Hirao* and Toru Amaya 

Synlett, 33 (15), 1492-1499 (2022).

https://doi.org/10.1055/s-0041-1738071

4.  Sustainable and Functional Redox Chemistry (Editor: Shinsuke Inagi)

Part 2, Chapter 5, Vanadium(V)-induced Oxidative Cross-coupling of Enolate Species 

Toru Amaya, Royal Society of Chemistry, April 2022.

Link

3.  Relevant synthesis to manipulating non-planarity in dibenzo[g,p]chrysene: Substitution reactions at the bay

Shinsuke Kamiguchi, Ryuhei Akasaka, Naruhiro Yoshida, Tomoya Imai, Yousuke Yamaoka, Toru Amaya, and Tetsuo Iwasawa* 

Tetrahedron Lett., 92 (2) 153664 (2022).

https://doi.org/10.1016/j.tetlet.2022.153664

2.  Overlooked Factors Required for Electrolyte Solvents in Li–O2 Batteries: Capabilities of Quenching 1O2 and Forming Highly-Decomposable Li2O2

Kiho Nishioka, Mizuki Tanaka, Hayato Fujimoto, Toru Amaya, Sensuke Ogoshi, Mamoru Tobisu, and Shuji Nakanishi* 

Angew. Chem. Int. Ed., 61 (12), e2021127 (2022).

https://doi.org/10.1002/anie.202112769

1.  9-Iodo-9-Borabicyclo[3.3.1]nonane

Toru Amaya 

Encyclopedia of Reagents for Organic Synthesis (e-EROS)

https://doi.org/10.1002/047084289X.rn02421

 2021

5.  有機電解合成の新潮流 監修:淵上寿雄、跡部真人、稲木信介

【第Ⅱ編 合成手法・応用】第4章 芳香族化合物の電解カップリング 

雨夜 徹、シーエムシー出版、2021年11月25日発行(pp.71-80)

Link

4.  Chemo- and regioselective cross-dehydrogenative coupling reaction of 3-hydroxycarbazoles with arenols catalyzed by a mesoporous silica-supported oxovanadium

Kengo Kasama, Kyohei Kanomata, Yuya Hinami, Karin Mizuno, Yuta Uetake, Toru Amaya, Makoto Sako, Shinobu Takizawa, Hiroaki Sasai, and Shuji Akai*

RSC Advances, 11 (56) 35342 - 35350 (2021). (Open Access)

https://doi.org/10.1039/D1RA07723F

3.  Solution-Processable Multi-Substituted Buckybowls: Synthesis of Diindeno(1,2,3,4-defg:1’,2’,3’,4’-mnop)chrysene Derivatives 

Naoki Yoshida, Ryuhei Akasaka, Yusuke Awakura, Toru Amaya, and Tetsuo Iwasawa* 

Eur. J. Org. Chem., (38) 5343-5347 (2021). (selected as a Cover Feature)

https://doi.org/10.1002/ejoc.202100869

Cover Feature:  https://doi.org/10.1002/ejoc.202101198

2.  Structural Consequences of Two-Fold Deprotonation of Sumanene: Embedding Two Cp-rings into a Nonplanar Carbon Framework 

Zheng Zhou, Zheng Wei, Toshikazu Hirao, Toru Amaya, and Marina A. Petrukhina* 

Organometallics, 40 (13), 2023–2026 (2021).

http://dx.doi.org/10.1021/acs.organomet.1c00295

1. スピロビフルオレンの連結に基づく構造的にユニークなπ共役系分子の合成

雨夜 徹

生産と技術, 73 (1), 51–54 (2021).

Link

 2020

4. Vanadium-induced Oxidative and Reductive Coupling

Toru Amaya and Toshikazu Hirao

In Vanadium Catalysis, Sutradhar, M.; Pombeiro, A. J. L.; Armando L da Silva, J. eds.; Royal Society of Chemistry; Chapter 19; pp 464–482. http://doi.org/10.1039/9781839160882-00464

3. Oxovanadium(v)-Catalyzed Oxidative Cross-Coupling of Enolates Using O2 as a Terminal Oxidant

Yuma Osafune, Yuqing Jin, Toshikazu Hirao, Mamoru Tobisu, Toru Amaya*

Chem. Commun., 56 (78), 11697–11700 (2020). 

http://dx.doi.org/10.1039/D0CC04395H

2. Pyrolysis of Iron‐Containing Polyanilines under Micropore Generation Control: Electrocatalytic Performance in the Oxygen Reduction Reaction

Yuhi Inada, Masato Daijo, Hitoshi Haneoka, Yosuke Murakami, Nao Eguchi, Toru Amaya, Takeyuki Suzuki, Takafumi Ohkawa, Ryotaro Tsuji, Toshikazu Hirao

ChemPlusChem, 85 (9), 1964–1967 (2020).  http://dx.doi.org/10.1002/cplu.202000363

1. Chiral Cyclic [n]Spirobifluorenylenes: Carbon Nanorings Consisting of Helically Arranged Quaterphenyl Rods Illustrating Partial Units of Woven Patterns

Kaige Zhu, Kosuke Kamochi, Takuya Kodama, Mamoru Tobisu, and Toru Amaya*

Chem. Sci., 11 (35) 9604–9610 (2020). http://dx.doi.org/10.1039/D0SC02452J

 2019

3. Linear [3]Spirobifluorenylene: An S-Shaped Molecular Geometry of p-Oligophenyls

Jumpei Oniki, Toshiyuki Moriuchi, Kosuke Kamochi, Mamoru Tobisu, and Toru Amaya* 

J. Am. Chem. Soc., 141 (45), 18238-18245 (2019).

http://dx.doi.org/10.1021/jacs.9b09179

本研究で合成した分子がThe Cambridge Crystallographic Data Centre (CCDC)で今月の”amazing new structure”として紹介された。

2. Recent Advances in Gomberg-Bachmann Biaryl Synthesis 

Toru Amaya*, Yuqing Jin, and Mamoru Tobisu

Tetrahedron Lett., 60 (39), 151062 (2019). (Digest review).

https://doi.org/10.1016/j.tetlet.2019.151062

1. Synthesis of a Sumanenyl Hafnocene Complex

Toru Amaya*, Shun Katoh, Toshiyuki Moriuchi, and Toshikazu Hirao*

Org. Chem. Front., 6(7) 1032-1037 (2019).

This article is part of the themed collection: In celebration of Julius Rebek’s 75th Birthday.

http://dx.doi.org/10.1030/c9qo00140a

 2018

5. Electrolytic Cross-Coupling of Arenediazonium Salts and Heteroarenes

Dai Hata, Mamoru Tobisu, and Toru Amaya*

Bull. Chem. Soc. Jpn., 59(12), 1749-1751 (2018). (Selected paper)

https://doi.org/10.1246/bcsj.20180193

4. レドックス型クロスカップリング反応の開発

雨夜 徹

化学工業 69(11), 807-811 (2018).

http://www.kako-sha.co.jp/

3. Iron(III) nitrate-induced aerobic and catalytic oxidative cleavage of olefins

Toru Amaya* and Hayato Fujimoto

Tetrahedron Lett., 59(27), 2657-2660 (2018).

 http://dx.doi.org/10.1016/j.tetlet.2018.05.070

2. Synthesis of self-doped polyaniline bearing phosphonic acid moiety via Pd-catalyzed phosphonation of poly(2-bromoaniline)

Toru Amaya*, Tomohiro Hatai, Izumi Kurata, and Toshikazu Hirao*

Tetrahedron Lett., 59(18), 1715-1718 (2018).

http://dx.doi.org/10.1016/j.tetlet.2018.03.054

. Synthesis and Isomerization Behavior of a Macrocycle with Four Photoresponsive Moieties

Toru Amaya*, Hayato Fujimoto, Takahiro Tanaka, and Toshiyuki Moriuchi

Org. Lett., 20(7), 2055-2058 (2018).

http://dx.doi.org/10.1021/acs.orglett.8b00598