OHGO Yoshiaki | Niigata College of Pharmacy

スポンサーリンク

概要

関連著者

もっと見る

著作論文

A Facile Synthesis of 2,3-Dihydroxyketones from 1,2-Diketones and Aldehydes Using Samarium Diiodide
Solid-State Specific and Unidirectional Photoisomerization of 3-Substituted Propyl to 1-Substituted Propyl Cobaloxime Complexes via 2-Substituted Propyl Complexes
Chiral Lattice-Controlled Asymmetric Photoisomerization of (2-Cyanoethyl)cobaloximes in the Solid State
The SmI_2 Mediated Cross-Coupling Reaction of Aldehydes with α-Diketones in Their Aqueous Forms
Asymmetric Synthesis of Ketones by SmI_2-Mediated Allylation or Benzylation of Ketenes Followed by Enantioselective Protonation
Crystalline-State Reaction of Cobaloxime Complexes. 18. Metastable Intermediate Structure Observed by a New X-Ray Diffractometer for Rapid Data Collection
Reactions in Solid and Constrained State. IV.^ Preparation and Solid-State Photoracemization of Optically Active Alkyl Cobaloxime Complexes
β-α Photoisomerization of Cobaloxime Complexes in the Solid State. 5.^ Reaction Rate Reduced by a Hydrogen Bond
Crystal Structure of [(S)-1, 2-Bis(allyloxycarbonyl)ethyl]bis-(dimethylglyoximato)[(R)-1-phenylethylamine]cobalt(III) Isopropanol Solvate
Structural studies of asymmetric hydrogenation. IV. The crystal structures of [(R)-1-cyanoethyl][(S)(-)-.ALPHA.-methylbenzylamine]bis(dimethylglyoximato)cobalt(III) at 293 K and 173 K.
Preparation and Reaction of Optically Active Organotransition Metal Complexes. III. Preparation of Optically Active (1-(Methoxycarbonyl)ethyl)cobaloximes Coordinated with Various Axial Ligands and Their Photoracemization. Remarkable Steric Effect of Axial
Preparation and reaction of optically active organotransition metal complexes. II. Preparation and photoracemization of optically active (1-cyanoethyl)cobaloxime complexes coordinated with various axial ligands.
Preparations and properties of optically active (alkyl)bis(dimethylglyoximato)cobalt(III) complexes.
Asymmetric hydrogenation catalyzed by bis(disubstituted glyoximato)cobalt(II)(L)-chiral cocatalyst system. Effect of structural variation of ligands and hydrogen pressure.
Asymmetric reactions. X. Asymmetric hydrogenation catalyzed by bis(dimethylglyoximato)cobalt(II)-chiral cocatalyst (amino alcohol) system.
Asymmetric hydrogenation catalyzed by the (achiral base)bis(dimethylglyoximato)cobalt(II)-chiral cocatalyst system. The preparation of a new type of chiral cocatalyst and its application to the asymmetric hydrogenation of methyl N-(acetylamino)acrylate an
Asymmetric hydrogenation of N,N'-dimethyl-5-alkylidene- and arylmethylenehydantoins catalyzed by (achiral base)bis(dimethylglyoximato)cobalt(II)-chiral cocatalyst system.
Asymmetric hydrogenation catalyzed by (achiral base)bis(dimethylglyoximato)cobalt(II)-chiral cocatalyst system.

もっと見る

スポンサーリンク