発表論文など

 

2023

Bathochromic Shift of Fluorescence Peak in Dipyrrolo[1,2-a:2,1′-c]quinoxaline by Introducing Each of Electron-Donating and Electron-Withdrawing Substituent,

Shoji Matsumoto, Makoto Takamori, Motohiro Akazzome, Molecules, 28 (7), 2896 (2023).

https://doi.org/10.3390/molecules28072896

ダイアグラム

自動的に生成された説明

 

Successful Identification of a Novel Therapeutic Compound for Hepatocellular Carcinoma through Screening of ADAM9 Inhibitors,

Keita Ogawa, Tetsuhiro Chiba, Masato Nakamura, Jun Arai, Jiaqi Zhang, Yaojia Ma, Na Qiang, Junjie Ao, Sae Yumita, Takamasa Ishino, Motoyasu Kan, Terunao Iwanaga, Miyuki Nakagawa, Kisako Fujiwara, Takafumi Sakuma, Hiroaki Kanzaki, Keisuke Koroki, Yuko Kusakabe, Kazufumi Kobayashi, Naoya Kanogawa, Soichiro Kiyono, Takayuki Kondo, Ryo Nakagawa, Sadahisa Ogasawara, Ryosuke Muroyama, Shingo Nakamoto, Tatsuo Kanda, Hitoshi Maruyama, Jun Kato, Shoji Matsumoto, Takayoshi Arai, Shinichiro Motohashi Naoya Kato, Anticancer Research, 43 (3), 1043-1052 (2023).

※当研究室で合成された化合物が活性評価されました。

 

 

2022

Relationship between Halogen-halogen Interaction and Electric Conductivity in Thiazolo[2,3-a]isoquinolin-7-ium Triiodides,

Shoji Matsumoto, Ryuta Sumida, Motohiro Akazzome, J. Mol. Struct., 1264, 133306 (2022).

https://doi.org/10.1016/j.molstruc.2022.133306

ダイアグラム, 概略図

自動的に生成された説明

 

 

2021

Chemoselective Reduction of α,β-Unsaturated Carbonyl and Carboxylic Compounds by Hydrogen Iodide,

Shoji Matsumoto, Hayato Marumoto, Motohiro Akazzome, Yasuhiko Otani, Tatsuo Kaiho, Bull. Chem. Soc. Jpn., 94 (2), 590-599 (2021).

https://doi.org/10.1246/bcsj.20200341

 

CCL299, a Benzimidazole Derivative, Induces G1 Phase Arrest and Apoptosis in Cancer Cells,

Yoshifumi Ohno, Ruipong Yi, Akiko Suganami, Yutaka Tamura, Akio Matsumoto, Shoji Matsumoto, Kengo Saito, Hiroshi Shirasawa, Anticancer Research, 41 (2), 699-706 (2021).

https://doi.org/10.21873/anticanres.14821

※当研究室で合成された化合物が活性評価されました。

 

 

2020

Change in the Fluorescence of 1,1′-Diaryl-2,2′-biimidazoles upon the Addition of Acid,

Shoji Matsumoto, Seigi Tachibana, Motohiro Akazome, Heterocycles, 100 (10), 1666-1677 (2020).

https://doi.org/10.3987/COM-20-14309

 

Molecular Recognition by Inclusion Crystals of Chiral Host Molecules Having Trityl and Related Bulky Groups,

Motohiro Akazome, Shoji Matsumoto, In Advances in Organic Crystal Chemistry, Comprehensive Reviews 2020, M. Sakamoto, H. Uekusa (Eds.): Springer, Tokyo, 2020,

pp. 457-475. (ISBN 978-981-15-5084-3)

 

 

2019

Selective Synthesis and Optical Properties of Diimidazo[1,2-a:5′,1′-c]quinoxaline Derivatives,

Shoji Matsumoto, Shunsuke Abe, Motohiro Akazome, Tetrahedron, 75 (26), 3657-3665 (2019).

https://doi.org/10.1016/j.tet.2019.05.041

Image 1

 

乙種1・2・3・5・6類危険物取扱者試験テキスト&問題集 第2版,

赤染元浩監修,ナツメ社,201931日発行 ISBN978-4-8163-6598-0.

乙1-6危険物 第2版

 

 

2018

Synthesis of Iodinated Thiazolo[2,3-a]isoquinolinium Salts and Their Crystal Strucutres with/without Halogen Bond,

Shoji Matsumoto, Ryuta Sumida, Sia Er Tan, and Motohiro Akazome, Heterocycles, 97 (2), 755-775 (2018).

https://doi.org/10.3987/COM-18-S(T)47

 

Selective Formation of Internal Olefinic Trimer of αMethylstyrenes with HI Gas and Ketones,

Shoji Matsumoto, Takehisa Oseki, Motohiro Akazome, and Yasuhiko Otani, ACS Omega, 3 (12), 17928-17935 (2018).

https://doi.org/10.1021/acsomega.8b03168

 

Preparation of Chiral 3-Oxocycloalkanecarbonitrile and Its Derivatives by Crystallization-Induced Diastereomer Transformation of Ketals with Chiral 1,2-Diphenylethane-1,2-diol,

Yohei Yamashita, Daisuke Maki, Shiho Sakurai, Takumi Fuse, Shoji Matsumoto, Motohiro Akazome, RSC Adv., 8 (57), 32601-32609 (2018).

https://doi.org/10.1039/c8ra06611f

Graphical abstract: Preparation of chiral 3-oxocycloalkanecarbonitrile and its derivatives by crystallization-induced diastereomer transformation of ketals with chiral 1,2-diphenylethane-1,2-diol

 

Exploiting CH/π Interactions in Robust Supramolecular Adhesives,

Taiki Yamate, Takayuki Fujiwara, Toru Yamaguchi, Hiroshi Suzuki, Motohiro Akazome, Polym. Chem., 9 (32), 4303-4308 (2018).

https://doi.org/10.1039/c8py00592c

Graphical abstract: Exploiting CH/π interactions in robust supramolecular adhesives 

                            (↑Inside front coverに選ばれました)

 

Incrementing Stokes Shifts through the Formation of 2,2′-Biimidazoldiium Salts,

Shoji Matsumoto, Mei Watanabe, Motohiro Akazome, Org. Lett., 20 (12), 3613-3617 (2018).

https://doi.org/10.1021/acs.orglett.8b01376

Figure

 

Polyacrylamide-Scaffold Adhesive Bearing Multiple Benzene Rings Forming CH/π Interactions with Polyolefin,

Taiki Yamate, Hiroshi Suzuki, Takayuki Fujiwara, Toru Yamaguchi, Motohiro Akazome, Adv. Mater. Lett., 9 (7), 526-530 (2018).

https://doi.org/10.5185/amlett.2018.2055

 

 

2017

Selective Reaction of Benzyl Alcohols with HI Gas: Iodination, Reduction, and Indane Ring Formations,

Shoji Matsumoto, Masafumi Naito, Takehisa Oseki, Motohiro Akazome, Yasuhiko Otani, Tetrahedron, 73 (52), 7254-7259 (2017).

https://doi.org/10.1016/j.tet.2017.11.009

image

 

Relationship between Mechanochromic Behavior and Crystal Structures in Donor-π-acceptor Compounds Consisted of Aromatic Rings with Ester Moiety as an Acceptor,

Shoji Matsumoto, Jun Moteki, Yuji Ito, Motohiro Akazome, Tetrahedron Lett., 58 (36), 3512-3516 (2017).

https://doi.org/10.1016/j.tetlet.2017.07.085

 

Effective Design of Supramolecular Polymer Adhesives Based on Multiple CH/π interactions,

Taiki Yamate, Hiroshi Suzuki, Kazuhisa Kumazawa, Takayuki Fujiwara, Toru Yamaguchi, Motohiro Akazome, Mol. Sys. Des. Eng., 2 (2), 214-222 (2017).

https://doi.org/10.1039/c7me00022g

Graphical abstract: Effective design of supramolecular polymer adhesives based on multiple CH/π interactions 

                                                  (↑Back coverに選ばれました)

 

完全攻略!ここが出る!毒物劇物取扱者試験テキスト&問題集

赤染元浩監修,ナツメ社,201781日発行 ISBN978-4-8163-6277-4.

 

A Practical and Scalable Synthesis of a Glucokinase Activator via Diastereomeric Resolution and Palladium-Catalyzed C–N Coupling Reaction,

Yohei Yamashita, Yasuhiro Morinaga, Makoto Kasai, Takao Hashimoto, Yuji Takahama, Atsushi Ohigashi, Satoshi Yonishi, Motohiro Akazome, Org. Process Res. Dev., 21 (3), 346-356 (2017).

https://doi.org/10.1021/acs.oprd.6b00415

Abstract Image

 

 

2016

一発合格!甲種危険物取扱者試験<ここが出る>問題集

赤染元浩監修,ナツメ社,201681日発行 ISBN978-4-8163-6061-9.

 

CH/π Interactions for Macroscopic Interfacial Adhesion Design,

Taiki Yamate, Kazuhisa Kumazawa, Hiroshi Suzuki, Motohiro Akazome, ACS Macro Lett., 5 (7), 858-861 (2016).

https://doi.org/10.1021/acsmacrolett.6b00265

Figure

 

Formation of Benzimidazoisoquinolinium and Benzimidazoisoindolinum Cyclic Systems by the Reaction of 2-(2-Alkynylphenyl)benzimidazoles with Iodine and Iodineiodine Interaction Including Halogen Bonding in Their Crystal Structures,

Shoji Matsumoto, Shu Kikuchi, Naoto Norita, Hyuma Masu, Motohiro Akazome, J. Org. Chem., 81 (13), 5322-5329 (2016).

https://doi.org/10.1021/acs.joc.6b00607

Figure

 

スパイラル有機化学−基礎から応用、発展へ!−

赤染元浩,河内 敦,松本祥治,三野 孝 著,筑波出版会,2016411日発行 ISBN978-4-924753-61-7

 

 

2015

一発合格!乙種第4類危険物取扱者試験<ここが出る>問題集

赤染元浩監修,ナツメ社,2015101日発行 ISBN978-4-8163-5902-6.

 

Chiral Recognition by Inclusion Crystals of Amino-Acid Derivatives Having Trityl Groups,

Motohiro Akazome, In Advances in Organic Crystal Chemistry, Comprehensive Reviews 2015, R. Tamura, M. Miyata (Eds.): Springer, Tokyo, 2015,

pp. 463-482. (ISBN 978-4-431-55554-4)

 

HI Gas as a Reagent for α-Alkylation Reaction with Two Ketone Molecules,

Shoji Matsumoto, Seigo Koitabashi, Yasuhiko Otani, Motohiro Akazome, Tetrahedron Lett., 56 (29), 4320-4323 (2015).

https://doi.org/10.1016/j.tetlet.2015.05.071

image

 

Systematic Investigation of Fluorescence Properties of Symmetric and Asymmetric Diazolo[1,2-a:2′,1′-c]quinoxaline Derivatives,

Shoji Matsumoto, Keisuke Sakamoto, Motohiro Akazome, Heterocycles, 91 (4), 795-814 (2015).

https://doi.org/10.3987/COM-15-13189

 

 

2014

一発合格!乙種第4類危険物取扱者試験テキスト&問題集

赤染元浩監修,ナツメ社,20141221日発行 ISBN978-4-8163-5761-9.

乙4表紙

 

多様な状態で蛍光発光可能な縮環型有機化合物群の開発

松本祥治,Jasco Report, 56 (1), 15-22 (2014).

 

Binding of Acetylcholine and Quaternary Ammonium Compounds to a Cs-Symmetric Bowl-Shaped Tripeptide of 2-(3-Aminophenyoxy)propanoic Acids Acting as a Ditopic Receptor,

Motohiro Akazome, Norihiro Hamada, Koji Takagi, Daisuke Yagyu, Shoji Matsumoto, Tetrahedron Lett., 55 (14), 2226-2229 (2014).

https://doi.org/10.1016/j.tetlet.2014.02.066

image

 

Formation of Benzo[c]thiophene-1-aminium Iodide by the Reaction of o-Alkynylbenzothioamide with Iodine,

Shoji Matsumoto, Daiki Takada, Hirokazu Kageyama, Motohiro Akazome, Tetrahedron Lett., 55 (5), 1082-1085 (2014).

https://doi.org/10.1016/j.tetlet.2013.12.094

Full-size image (10 K)

 

Synthesis and Optical Properties of 2,2'-Biimidazole and Benzo[d]imidazole Derivatives: Changing π-Conjugation by Photoexcitation,

Shoji Matsumoto, Yu Zhao, Motohiro Akazome, Heterocycles, 88 (1), 261-273 (2014).

https://doi.org/10.3987/COM-13-S(S)12

 

 

2013

Fluorescence of Diimidazo[1,2-a:2′,1′-c]quinoxalinium Salts Under Various Conditions,

Shoji Matsumoto, Hajime Abe, Motohiro Akazome, J. Org. Chem., 78 (6), 2397-2404 (2013).

https://doi.org/10.1021/jo302531g

Figure

 

α-Diketone Formation Accompanied by Oxidation of Sulfur Functional Group by the Reaction of o-Alkynylarenesulfoxide with Iodine,

Shoji Matsumoto, Hiroyuki Shibata, Motohiro Akazome, J. Org. Chem., 78 (4), 1650-1654 (2013).

https://doi.org/10.1021/jo3023186

Figure

 

Enantioselective Inclusion of Amide Guests into a Chiral N,N-Ditrityl Amino Amide Host to Compensate the Loss of Hydrogen Bonds Broken by Installation of Trityl Groups,

Ken Megumi, Shohei Yokota, Shoji Matsumoto, Motohiro Akazome, Tetrahedron Lett., 54 (7), 707-710 (2013).

https://doi.org/10.1016/j.tetlet.2012.12.029

image

 

 

さらに過去の論文などはこちらから。

 

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