九州大学大学院薬学研究院
環境調和創薬化学分野

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2019

Megumi Noshita, Yuhei Shimizu, Hiroyuki Morimoto, Shuji Akai, Yoshitaka Hamashima, Noriyuki Ohneda, Hiromichi Odajima, Takashi Ohshima
Ammonium Salt-Accelerated Hydrazinolysis of Unactivated Amides: Mechanistic Investigation and Application to a Microwave Flow Process
Org. Process Res. Dev. 2019, 23, 588–594. DOI: 10.1021/acs.oprd.8b00424



Yohei Matsumoto, Taro Tsuji, Daiki Nakatake, Ryo Yazaki, Takashi Ohshima
Thionoesters as 1,2‐Dipolarophiles for [4+2] Cycloaddition with Cyclobutanones
Asian J. Org. Chem. 2019, 8, 1071–1074.  DOI: 10.1002/ajoc.201900156

Seiya Taninokuchi, Ryo Yazaki, Takashi Ohshima
Mechanistic Insight into Catalytic Aerobic Chemoselective α-Oxidation of Acylpyrazoles
Heterocycles 2019, 99, 906–918. DOI: 10.3987/COM-18-S(F)58

Yuta Kondo, Kazuhiro Morisaki, Yoshinobu Hirazawa, Hiroyuki Morimoto, Takashi Ohshima
A Convenient Preparation Method for Benzophenone Imine Catalyzed by Tetrabutylammonium Fluoride
Org. Process Res. Dev. 2019, 23, 1718–1724. DOI: 10.1021/acs.oprd.9b00226


Ryo Yazaki, Takashi Ohshima
Cross-Dehydrogenative Coupling of Carbonyls for Heterocycle Synthesis
Heterocycles via Cross Dehydrogenative Coupling 2019, 213–229. DOI: 10.1007/978-981-13-9144-6_6


Hiroyuki Morimoto, Walaa Akkad, Toru Deguchi, Takashi Ohshima
Mechanistic Studies of Nickel(II)-Catalyzed Direct Alcoholysis of 8-Aminoquinoline Amides
Heterocycles, Prepress. DOI: 10.3987/COM-19-S(F)30

Ryo Yazaki, Takashi Ohshima
Recent strategic advances for the activation of benzylic C–H bonds for the formation of C–C bonds
Tetrahedron Lett. 2019, 60, 151225. DOI: 10.1016/j.tetlet.2019.151225

Takuya Yokoyama, Masaki Yukuhiro, Yuka Iwasaki, Chika Tanaka, Kazunari Sankoda, Risa Fujiwara, Atsushi Shibuta, Taishi Higashi, Keiichi Motoyama, Hidetoshi Arima, Kazumasa Yoshida, Nozomi Sugimoto, Hiroyuki Morimoto, Hidetaka Kosako, Takashi Ohshima, Masatoshi Fujita
Identification of candidate molecular targets of the novel antineoplastic antimitotic NP-10
Scientific Reports, 2019, 9, Article number: 16825. DOI: 10.1038/s41598-019-53259-2