田口胤三 | Faculty Of Pharmaceutical Sciences Kyushu University

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著作論文

Catalytic Rearrangement of O, S-Dialkyl Dithiocarbonates to S, S-Dialkyl Dithiocarbonates. IV. Use of Boron Trifluoride Etherate as Catalyst
Rearrangement and trans-Elimination contrary to the Chugaev Reaction Rule. XIII. Solvent Effect on Rearrangement Reaction of Allylic Xanthates and a Correction of the Former Report
Catalytic Rearrangement of Xanthates to Dithiolcarbonates
Rearrangement and trans-Elimination contrary to the Chugaev Reaction Rule. IX. Thermal Rearrangement of 2-Cycloalkenyl S-Alkyl Xanthate
Rearrangement and trans-Elimination contrary to the Chugaev Reaction Rule. VIII. Thermal Rearrangement of 2-Alkenyl S-Alkyl Xanthate
Heteroalicyclic Aminoalkanol. II. Reactions of DL-2-Piperidinemethanol involving the Formation of DL-1-Azabicyclo[4,1,0]heptane
Heteroalicyclic Aminoalkanol. I. Syntheses of DL-2-Piperidinemethanol and meso-cis-2,6-Piperidinedimethanol and Reactions of Intermediates
thionamides. I. Synthesis. Demethylation of their N, N-Dimethyl Derivatives by Sulfur.
Deamination Reaction of Diastereomeric DL-2 (1-Phenylcyclohexyl) cyclohexylamine with Nitrous Acid
Grignard Reaction and Products. V. Reduction of Ketoximes to Aziridines with Grignard Reagents
Grignard Reaction and Products. VI. The Reaction of Grignard Reagents with 2-Phenoxy-and 2-Benzyloxy-cyclohexanone Oximes
Sulfinylamine Chemistry. I. A New Degradation Reaction of α-Amino Acid with N-Sulfinylaniline
Grignard Reaction and Products. II. A Novel Intramolecular Cyclization in the Grignard Reaction of Alicyclic Ketoxime containing an Aromatic Nucleus
Grignard Reaction and Products. I. 1,4-Addition of Arylmagnesium Bromide to 2-Alkylidenecyclohexanone and the Oxidative Cleavage therein
Configurational Effect in N-Alkylation of Diastereomeric 2-Aminocyclohexanol.

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