S
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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Miniaturization and Combinatorial Approach in Organic Electrochemistry
TL;DR: Recent advances in electro-organic chemistry involving miniaturization, integration, and combinatorial chemistry were reviewed and batch and flow electrolysis systems for the optimization and screening of electro- organic reactions as well as the building of chemical libraries for organic compounds are described.
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Reduction of a "cation pool": a new approach to radical mediated C--C bond formation.
TL;DR: The present strategy opens new opportunities to manipulate reactive carbon species using redox processes in organic synthesis by examining electrochemical reduction of "cation pools" generated by low-temperature electrolysis of carbamates.
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Three-component coupling based on the "cation pool" method.
TL;DR: In this paper, an N-acyliminium ion generated by thecation pool method adds to an electron-rich carbon−carbon double bond, such as enamine derivatives and vinyl sulfides, to form the second "cation pool" to create the corresponding three-component coupling products.
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Generation of alkoxycarbenium ion pools from thioacetals and applications to glycosylation chemistry
TL;DR: A one-pot method for electrochemical glycosylation, which involves anodic oxidation of thioglycosides to generate Glycosyl cation equivalents followed by their reactions with glycosy acceptors, has been developed.
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Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions
Hiroki Mandai,Kazuki Fujii,Hiroshi Yasuhara,Kenko Abe,Koichi Mitsudo,Toshinobu Korenaga,Seiji Suga +6 more
TL;DR: It is demonstrated that by attaching a binaphthyl moiety, appropriately modified to establish H-bonding interactions within the key intermediates in the catalytic cycle, and a 4-aminopyridyl unit, exceptionally efficient organic molecules can be prepared that facilitate enantioselective acyl transfer reactions.