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Seiji Suga

Researcher at Okayama University

Publications -  204
Citations -  6857

Seiji Suga is an academic researcher from Okayama University. The author has contributed to research in topics: Nucleophile & Catalysis. The author has an hindex of 44, co-authored 192 publications receiving 6313 citations. Previous affiliations of Seiji Suga include Nagoya University & Kyoto University.

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Electro-reductive cyclization of aryl halides promoted by fluorene derivatives

TL;DR: In the presence of fluorene derivatives, the electro-reduction of aryl chlorides, bromides, and iodides bearing an ethylene moiety proceeded smoothly to afford the corresponding cyclized products as discussed by the authors.
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Desymmetrization of meso-1,2-Diols by a Chiral N,N-4-Dimethylaminopyridine Derivative Containing a 1,1'-Binaphthyl Unit: Importance of the Hydroxy Groups.

TL;DR: An acylative desymmetrization of meso-1,2-diols using a binaphthyl-based N,N-4-dimethylaminopyridine derivative 1h with tert-alcohol substituents to provide a monoacylate selectively with a high enantiomeric ratio is developed.
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Dynamic Kinetic Resolution of Azlactones by a Chiral N, N-Dimethyl-4-aminopyridine Derivative Containing a 1,1'-Binaphthyl Unit: Importance of Amide Groups.

TL;DR: A dynamic kinetic resolution (DKR) of azlactones in the presence of benzoic acid and a binaphthyl-based N, N-4-dimethylaminopyridine derivative 1i having two amide groups at the 3,3'-positions of a binAPHthyl unit is developed.
Journal Article

Synthetic Terrein Inhibits Progression of Head and Neck Cancer by Suppressing Angiogenin Production.

TL;DR: The mechanism underlying the anti-tumor effects of synthetic terrein against head and neck cancer consists of the inhibition of both tumor cell proliferation and angiogenesis via the suppression of ANG production.
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Electro-reductive Halogen-Deuterium Exchange and Methylation of Aryl Halides in Acetonitrile

TL;DR: In this article, the first electro-reductive halogen-deuterium exchange reaction and methylation reaction was reported under metal-free and mild conditions, and the reaction in CD3CN gave deuterated product selectively.