Kawai Y | Institute For Chemical Research Kyoto University

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著作論文

Efficient Synthesis, Structure, and Redox Reactions of 1,4,6,9-Tetraisopropylchalcogenanthrenes
Synthesis of New Pentathiepin and Dithiatriselenepin Fused to Ferrocene via Dithiametallacycles
Design of Reversible Low Redox Potential Systems Using Five-Membered Trichalcogenaheterocycles Containing Heavy Chalcogens ; Sulfur, Selenium, and Tellurium
Preparation of Functionalized Thianthrenes and Their Higher Related Compounds by Photolysis of Benzotrithiole Derivatives
Generation and Detection of a Dithia Dication Derived from 4,9-Diethyl-[1,4]dihydrodithiino[5,6-f]benzotrithiole 5-Oxide and Its Disproportionation
Preparation and Conformational Analysis of 6,10-Diethyl[1,2,3]trithiolo-[4,5-h]benzopentathiepin Monoxides : Isolation and Optical Properties of Chiral Benzopentathiepin Derivatives
First Preparation and Structural Determination of Optically Pure Cyclic Polysulfides, 6, 10-Diethyl Trithiolo[h]benzopentathiepin Monooxides
Synthesis and Unique Packing Structure by X-Ray Analysis of New Types of Stable Trithioles Bound to Fused Aromatic Systems
Synthesis, Structure, and Oxidation of Novel 4,7-Disubstituted Benzotrithioles. Formation and Characterization of Radical Cations with 11πElectron Framework
Reactivities of Stable Rotamers. XLI. Reactions of 1-(9-Fluorenyl)-2-(1-methylethenyl)naphthalene Rotamers with Chalcogenyl Halides and Observation of Coloration During the Reaction of Methanesulfenyl Chloride and the ap-Rotamer
Conformational Effect (Induced-Fit) on Catalytic Activity of α-Chymotrypsin
Stereochemical Control in Microbial Reduction. XXIX. Mechanism of Stereochemical Control with an Additive in the Diastereoselective Reduction by Geotrichum candidum
Stereochemical Control in Microbial Reduction. XXV. Additives Controlling Diastereoselectivity in a Microbial Reduction of Ethyl 2-Methyl-3-oxobutanoate

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