Shigetaka Yakabe
Tokyo University of Agriculture and Technology
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Publication
Featured researches published by Shigetaka Yakabe.
Synthetic Communications | 1996
Masao Hirano; Shigetaka Yakabe; James H. Clark; Hiroyuki Kudo; Takashi Morimoto
Abstract A wide variety of sulphides can be readily converted to the corresponding sulphoxides in good to excellent yields by treatment with a combination of sodium chlorite, (salen)manganese(III) complex, and chromatographic alumina in dichloromethane under mild and neutral conditions.
Synthetic Communications | 2006
Masao Hirano; Shigetaka Yakabe; Masataka Fukami; Takashi Morimoto
Abstract — Aromatic, aliphatic, and alicyclic thiols can be readily oxidized to the disulfides quantitatively by calcium hypochlorite and moist Montmorillonite K10 under mild and neutral conditions.
Synthetic Communications | 1998
Shigetaka Yakabe; Masao Hirano; Takashi Morimoto
Chlorination of a variety of aliphatic, alicyclic, and aromatic ketones with a reagent combination of NaClO2 and Mn(acac)3 catalyst can be readily performed in dichloromethane to afford α-chloroket...
Tetrahedron Letters | 2000
Shigetaka Yakabe; Masao Hirano; Takashi Morimoto
Abstract Aliphatic and aromatic alkenes were hydrogenated quantitatively to the corresponding alkanes with sodium borohydride, catalyzed by nickel chloride in the presence of moist alumina in hexane under mild conditions.
Synthetic Communications | 1996
Masao Hirano; Shigetaka Yakabe; Akiko Satoh; James H. Clark; Takashi Morimoto
Abstract A variety of unsubstituted and mono- or di-substituted cycloalkanones can be oxidised with modest excess of magnesium monoperoxyphthalate hexahydrate in acetonitrile to produce the corresponding lactones in a facile, selective, and high yielding manner.
Synthetic Communications | 1998
Masao Hirano; Shigetaka Yakabe; Hiroyuki Monobe; Takashi Morimoto
Abstract Regioselective and high-yielding nuclear monobromination of aromatic ethers can be accomplished with a combination of NaClO2, NaBr, and Mn(acac)3 catalyst in dichloromethane under mild and neutral conditions with the aid of Montmorillonite K10.
Synthetic Communications | 1998
Masao Hirano; Hiroyuki Monobe; Shigetaka Yakabe; Takashi Morimoto
Abstract Nuclear monobromination of aromatic ethers can be achieved with a NaClO2/NaBr/Mn(acac)3 catalyst/silica gel system in dichloromethane in regioselective and high-yielding manner under mild conditions.
Synthetic Communications | 1997
Masao Hirano; Shigetaka Yakabe; Takashi Morimoto
Abstract 1,3-Dithianes derived from aromatic, aliphatic, and alicyclic ketones or aldehydes can be conveniently converted to the parent carbonyl compounds with a combination of ferric nitrate and silica gel in hexane in excellent to quantitative yields.
Synthetic Communications | 1998
Shigetaka Yakabe; Masao Hirano; Takashi Morimoto
Abstract Aliphatic, alicyclic, and aromatic alkenes underwent smooth vic-dichlorination upon treatment with a reagent combination of NaClO2, Mn(acac)3 catalyst, and chromatographic neutral alumina preloaded with a small amount of water in dichloromethane under mild conditions.
Synthetic Communications | 1997
Masao Hirano; Shigetaka Yakabe; Hiroyuki Monobe; James H. Clark; Takashi Morimoto
Abstract A combination of sodium chlorite, (salen)manganese(III) catalyst, and chromatographic neutral alumina in dichloromethane can be successfully utilized for the aromatic monochlorination of a variety of alkyl phenyl ethers in excellent to quantitative yields under mild and anhydrous conditions.