学術研究・イノベーション推進機構
研究者氏名 西田 篤司
ニシダ アツシ URL 所属 千葉大学 部署 学術研究・イノベーション推進機構 職名 特任教授 学位 薬学博士(北海道大学) J-Global ID 200901074908564750
研究キーワード
有機合成化学
,synthetic organic chemistry
受賞
2020年3月
日本薬学会, 薬学会賞,新規反応開発を基盤とする多環性天然物合成
2004年3月
日本薬学会, 学術振興賞,新規骨格構築法の開発と天然物合成への応用
論文
Shigeru Arai Arisa Izaki Yuka Amako Masaya Nakajima Masanobu Uchiyama Atsushi Nishida
Advanced Synthesis and Catalysis 361(21) 4882-4887 2019年11月 [査読有り]
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim A Ni-catalyzed [2+2+2] cycloaddition reaction between allene-ynes and various mono-, di- and tri-substituted allenes is described. This protocol effectively differentiates allenyl π components and ...
Shigeru Arai Yuna Kawata Yuka Amako Atsushi Nishida
Tetrahedron Letters 60(43) 2019年10月 [査読有り]
© 2019 Elsevier Ltd A nickel-catalyzed [2 + 2] cycloaddition of bisallenes has been described. Simple bisallenes are employed for the formation of “head to head” cycloadducts in the presence of Ni(0) with xantphos. The dienyl moiety in a product w...
Akito Okabe Shinji Harada Takuya Takeda Atsushi Nishida
European Journal of Organic Chemistry 2019(24) 3916-3920 2019年6月 [査読有り]
Shinji Harada Atsushi Nishida
Asian Journal of Organic Chemistry 8(6) 732-745 2019年6月 [査読有り]
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Diels-Alder reaction is one of the most well-known named reactions in organic chemistry. It involves a diene substrate and a dienophile substrate. Among dienes, siloxydiene is a reactive substrate ...
Shigeru Arai Koichi Nakazawa Xiao fei Yang Atsushi Nishida
Tetrahedron 75(17) 2482-2485 2019年4月 [査読有り]
© 2019 Nickel-catalyzed regioselective hydrocyanation of terminal alkynes is described. A tosylamide functionality at the propargyl position was the most suitable group for controlling the regiochemistry for C–CN bond formation as well as rate enh...
MISC
Shigeru Arai Yuka Amako Hiroto Hori Atsushi Nishida
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry 77(4) 341-350 2019年 [査読有り]
© 2019 Society of Synthetic Organic Chemistry. All rights reserved. Since a cyano group can be transformed to carboxylic acids, amino- and hydroxymethyl groups as well as aldehydes, its installation, particularly catalytic protocol, has been one o...
Shigeru Arai Masaya Nakajima Atsushi Nishida
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry 76(7) 668-677 2018年 [査読有り]
© 2018 Society of Synthetic Organic Chemistry. Lundurines A-D were isolated in 1995 from the Malayan plant Kopsia tenuis, which has been used in folk medicine and is a rich source of biologically active alkaloids. Their intriguing hexacyclic frame...
Shigeru Arai Masaya Nakajima Atsushi Nishida
Alkaloids: Chemistry and Biology 78 167-204 2017年 [査読有り]
© 2017 Elsevier Inc. This review focuses on the total synthesis of lundurines A–C. Their main structural feature is a unique cyclopropa[b]indole core that has been found only in these alkaloids. In addition to this characteristic structure, the bi...
Minoru Isobe Atsushi Nishida Yeun-Mun Choo Noorsaadah Abd. Rahman Poonsakdi Ploypradith Somsak Ruchirawat Guo-Qiang Lin Ang Li Zhu-Jun Yao Biing-Jiun Uang Chun-Chen Liao Pauline Chiu Byeong Moon Kim Teck Peng Loh
Chemistry - An Asian Journal 10(4) 790-804 2015年 [査読有り]
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry 73(3) 254-265 2015年
We have established aromatic enamide-ene metathesis to give highly substituted indole derivatives. This is a new method for the preparation of chiral 2-trans-cyclopropyl indoles, which successfully led to our H 4 antagonist candidates. Based on th...
大学院国際学術研究院