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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Journal ArticleDOI
The Tandem Michael-aldol Reaction Catalyzed by Trityl Perchlorate
Teruaki Mukaiyama,Shu Kobayashi +1 more
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An Efficient Asymmetric Aldol Reaction Promoted by a Chiral Tin(II) Lewis Acid Consisting of Tin(II) Triflate, (R)-2-[(N-1-Naphthylamino)methyl]tetrahydrothiophene and a Tin(IV) Compound
TL;DR: In this article, the chiral Lewis acid was successfully employed in the enantioselective aldol reactions of silyl enol ether of S-ethyl propanethioate with achiral aldehydes to afford the corresponding adducts.
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Asymmetric reduction of prochiral hydroxy ketones with a chiral reducing agent prepared from tin(ii) chloride, a chiral diamine, and diisobutylaluminum hydride
TL;DR: Asymmetric reduction of prochiral α- and β-hydroxy ketones with a reagent, generated from tin(II) chloride, a chiral diamine, and diisobutylaluminum hydride, afforded the corresponding dihydroxy compounds in good chemical and optical yields as mentioned in this paper.
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Syntheses and Reactions of 2-Ethylthio- or 2-Phenylthio-2-cycloalkenones
TL;DR: In this paper, it was shown that dihydrofuran derivatives were obtained in good yields from the sulfonium salts of the cycloalkenones and active methylene compounds.
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Tin(ii) enediolate from methylglyoxal
TL;DR: Methylglyoxal is successfully converted to the tin(II) enediolate on treatment with activated metallic tin and reacts with several aldehydes to give α, β-dihydroxyketones in good yields.