T
Teruaki Mukaiyama
Researcher at Kitasato University
Publications - 1072
Citations - 15343
Teruaki Mukaiyama is an academic researcher from Kitasato University. The author has contributed to research in topics: Catalysis & Silylation. The author has an hindex of 52, co-authored 1072 publications receiving 14878 citations. Previous affiliations of Teruaki Mukaiyama include University of Tokyo & Tokyo University of Science.
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S-Alkylthioamidium Salt. II. The Reactions of S-Alkylthioamidium Iodides with Mercuric Compounds
TL;DR: In this paper, the reactions of S-alkylthioamidium iodides with some mercuric compounds have been studied and it was established that the reaction of mercurics cyanide with the iodides afforded α-dimethylaminomalononitriles by the elimination of alkylmercaptomercuric iodide.
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Dehydration Reactions of Benzaldoxime by Means of Compounds Having a Nitrogen-Carbon Double Bond
TL;DR: In this article, the dehydration reactions of benzaldoxime with such nitrogen-carbon double bond compounds having halogen and alkoxyl groups as phenylimidophosgen, ethyl N-phenyliminochlo-roformate and ethyl n-phenylformidate were studied.
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A total synthesis of (.+-.)-integerrimine.
TL;DR: A total synthesis of a 12-membered bislactonic pyrrolizidine alkaloid, integerrimine, has been achieved in this paper, which is known as the first synthesis of integerrimines.
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A Novel Activating Agents of ‘Disarmed’ Thioglycosides, Combination of Trityl Tetrakis(pentafluorophenyl)borate, Iodine and 2,3-Dichloro-5,6-dicyano-p-benzoquinone (DDQ)
TL;DR: A combined use of trityl tetrakis(pentafluorophenyl) borate, iodine, and 2,3-dichloro-5,6-dicyano-p-benzoquinone effectively activates “disarmed” thioglycosides to afford the corresponding disaccharides in high yields on treatment with several glycosyl acceptors.
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5,6-dihydrophenanthridin-5-yl as an activatable protecting group of carboxylic acid—a direct preparation of amides from 5-acyl-5,6-dihydrophenanthridine
TL;DR: In this article, various amides are directly prepared from the protected carboxylic acids, 5-acyl-5,6-dihydrophenanthridines, by the reaction with primary amines in the presence of cerie pyridinium chloride and cupric oxide.