K
Koji Kato
Researcher at Mitsui Chemicals
Publications - 38
Citations - 643
Koji Kato is an academic researcher from Mitsui Chemicals. The author has contributed to research in topics: Catalysis & Cobalt. The author has an hindex of 14, co-authored 38 publications receiving 592 citations.
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Journal ArticleDOI
Oxidation-Reduction Hydration of Olefins with Molecular Oxygen and 2-Propanol Catalyzed by Bis(acetylacetonato)cobalt(II)
TL;DR: In the presence of a catalytic amount of bis(acetylacetonato)cobalt(II), various olefins are hydrated with oxygen and secondary alcohol to afford the corresponding alcohols together with alkanes and ketones via Oxidation-Reduction process as mentioned in this paper.
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A New and Facile Method for the Direct Preparation of α-Hydroxycarboxylic Acid Esters from α,β-Unsaturated Carboxylic Acid Esters with Molecular Oxygen and Phenylsilane Catalyzed by Bis(dipivaloylmethanato)manganese(II) Complex
TL;DR: In this paper, the authors proposed a new and convenient method for the direct preparation of various α-hydroxy carboxylic acid esters starting from α,β-unsaturated CARB esters, and studied the influence of substituents of olefins on regioselectivity.
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Catalytic oxidation-reduction hydration of olefin with molecular oxygen in the presence of bis(1,3-diketonato)cobalt(II) complexes.
TL;DR: In the presence of a bis(1,3-diketonato)cobalt(II) complex, various olefins are converted to the corresponding hydrated products according to the Markownikov rule on treatment with molecular oxygen in secondary alcohol (“oxidation-reduction hydration”) as mentioned in this paper.
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The Baeyer-Villiger oxidation of ketones catalyzed by nickel (II) complexes with combined use of molecular oxygen and an aldehyde.
TL;DR: In the presence of a catalytic amount of a nickel(II) complex coordinated with 1,3-diketone, various cyclic or acyclic ketones are converted into the corresponding lactones or esters by the Baeyer-Villiger oxidation on treatment with an atmospheric pressure of molecular oxygen (oxidant) and an aldehyde (reductant) at room temperature as discussed by the authors.
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Bis(trifluoroacetylacetonato)cobalt(II) catalyzed oxidation-reduction hydration of olefins selective formation of alcohols from olefins
TL;DR: In this article, various olefins are hydrated with molecular oxygen (oxidant) and a secondary alcohol (reductant) in the presence of a catalytic amount of bis(trifluoroacetylacetonato)cobalt(II) in good yields.