The reactive intermediate of catalytic borohydride reduction by Schiff base-cobalt complexes

Izumi Iwakura, Miho Hatanaka, Ai Kokura, Haruna Teraoka, Taketo Ikeno, Takushi Nagata, Tohru Yamada

研究成果: Article

20 引用 (Scopus)

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The key reactive intermediate of borohydride reduction catalyzed by Schiff base-cobalt complexes is proposed to be the dichloromethylcobalt hydride with a sodium cation, based on experimental and theoretical studies. It was revealed that chloroform is not the solvent but the reactant that activates the cobalt catalyst. The substrate carbonyl compounds are fixed and activated by the alkali cation, which is cap tured by the oxygen atoms of the planar ligand and the chlorine atom of the axial ligand, and attacked by the hydride on the cobalt atom via a sixmembered-like transition state to afford the corresponding alcohol.

元の言語English
ページ(範囲)656-663
ページ数8
ジャーナルChemistry - An Asian Journal
1
発行部数5
DOI
出版物ステータスPublished - 2006 12 11

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry

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