A
A. Ando
Researcher at Nagoya City University
Publications - 12
Citations - 283
A. Ando is an academic researcher from Nagoya City University. The author has contributed to research in topics: Enantioselective synthesis & Aldol reaction. The author has an hindex of 5, co-authored 12 publications receiving 277 citations.
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Journal ArticleDOI
New methods and reagents in organic synthesis. 75. asymmetric synthesis of α-hydroxy ketones using chiral phase transfer catalysts
TL;DR: Optically active α-hydroxy ketones are obtained by oxidation of achiral ketones with molecular oxygen in two phase system using chiral phase transfer catalysts.
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Chiral quarternary ammonium fluoride. A new reagent for catalytic asymmetric aldol reactions
TL;DR: In this paper, a chiral quarternary ammonium fluoride was used for catalytic enantioselective aldol reactions of silyl enol ethers with benzaldehyde in high enantiomeric excesses.
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Chemical Manganese Dioxide (CMD), an Efficient Activated Manganese Dioxide. Application to Oxidation of Benzylic and Allylic Alcohols
Toyohiko Aoyama,Naoko Sonoda,M. Yamauchi,K. Toriyama,Masahiro Anzai,A. Ando,Takayuki Shioiri +6 more
TL;DR: In this paper, it is shown that activated manganese dioxide (MnO2) is a useful reagent both for selective oxidation of benzylic and allylic alcohols to aldehydes and ketones, respectively, and for dehydrogenation of heterocycles to heteroaromatics.
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Enantioselective synthesis of β-hydroxy-α-methyl carbonyl compounds by aldol reaction
A. Ando,Takayuki Shioiri +1 more
TL;DR: The enantioselective aldol reactions of ketone lithium enolates with aldehydes mediated chiral lithium amides were extensively investigated in this paper, where the chiral amino ethers 4a, 4l and diamines 16a, b were prepared from α-amino acids.
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Studies on Reaction Conditions and New Entry to Chiral Ligands in the Chiral Lithium Amide-Mediated Enantioselective Aldol Reaction
TL;DR: In this article, the chiral lithium amide 6b was used as a chiral auxiliary for the enantioselective aldol reaction of 2, 2-dimethyl-3-pentanone and benzaldehyde.