大石武 | Riken Institute (The Institute of Physical and Chemical Research)

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著作論文

The Regioselective Dehydration of Unsymmetrical Secondary Alcohols under Mitsunobu's Reaction Conditions
ENZYMATIC HYDROLYSIS IN ORGANIC SOLVENTS FOR KINETIC RESOLUTION OF WATER-INSOLUBLE α-ACYLOXY ESTERS WITH IMMOBILIZED LIPASES
A Facile Chemoenzymatic Route to Optically Active 4,5-Disubstituted-2E-hexenoate Derivatives. I
Enantioselective Acetylation of an α-Hydroxy Ester by Using Ether-Linked Lipid-Lipase Aggregates in Organic Solvents
A Lipid-Lipase Aggregate with Ether Linkage as a New Type of Immobilized Enzyme for Enantioselective Hydrolysis in Organic Solvents
A FACILE CHEMOENZYMATIC ROUTE TO ENANTIOMERICALLY PURE 4,5-DISUBSTITUTED-2-HEXENOATE DERIVATIVES
A LIPID LIPASE AGGREGATE AS A NEW TYPE OF IMMOBILIZED ENZYME
Asymmetric Reduction of α-Methyl β-Keto Esters by Microbial Cells Immobilized with Prepolymer(Organic,Chemical)
SYNTHESIS OF USEFUL CHIRAL SYNTHONS (2R, 3R)-2-METHYLMALATE AND ITS CONGENERS VIA MICROBIAL ASYMMETRIC REDUCTION
Reduction of Nitroolefin Using Microorganisms
Synthesis of (+)- and (-)-cis-α-Irones
Studies on Taxane Synthesis III.Stereocontrolled Synthesis of a Twelve-Membered Lactam Sulfide as a Precursor of 4,8,11,11-Tetramethyl-3-oxobicyclo[5.3.1]undec-8-ene
Studies on Taxane Synthesis. II. : Synthese of 3,8,11,11-Tetramethyl-4-oxo- and 4,8,11,11-Tetramethyl-3-oxo-bicyclo[5.3.1]undec-8-enes Corresponding to the A- and B-Rings of Taxane Diterpenes
Studies on Taxane Synthesis. I. : Synthesis of 3,8,11,11-Tetramethyl-4-oxobicyclo[5.3.1]undecane as a Model for Taxane Synthesis
Revised Stereostructure for (+)-Roemecarine and Synthesis of (±)-, (+)-, and (-)-Roemercarine and (±)-Epiroemecarine
Kinetic Resolution of (±)-4-Acyloxy-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisopuinolines by Use of Immobilized Lipases in Organic Solvents
DETERMINATION OF THE STEREOSTRUCTURE OF THE δ-LACTONES OF 5,7-DIHYDROXY-2,3-UNSATURATED ACIDS BY ^1H NMR SPECTROSCOPY(Communications to the Editor)
Formal Total Synthesis of (-(-Indolmycin
A Facile Chemoenzymatic Route to Optically Active 4,5-Disubstituted-2E-hexenoate Derivatives. II
β-HYDROXY-δ-LACTONES AS CHIRAL BUILDING BLOCKS INVOLVING 1,3-DIHYDROXYL FUNCTIONS. 1. : NEW STRATEGIES FOR STREOSELECTIVE CONSTRUCTION OF 2-METHYL-3,5-DIHYDROXY ESTERS
Highly syn-Selective Reduction of α-Phenylthio-β-methoxy Ketones with Super-hydride

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