鴻巣俊之 | Medicinal Chemistry Research Laboratories Sankyo Co. Ltd.

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PAYNE REARRANGEMENT ROUTE TO THE OPTICALLY ACTIVE OXIRANE PRECURSOR FOR THE PREPARATION OF TRIAZOLE ANTIFUNGALS
Triazole Antifungals. IV. Synthesis and Antifungal Activities of 3-Acylamino-2-aryl-2-butanol Derivatives
Triazole Antifungals. III. Stereocontrolled Synthesis of an Optically Active Triazolylmethyloxirane Precursor to Antifungal Oxazolidine Derivatives
Triazole Antifungals. II. : Synthesis and Antifungal Activities of 3-Acyl-4-methyloxazolidine Derivatives
Triazole Antifungals. V. Synthesis and Antifungal Activities of Some Amides Related to 3-Acylamino-2-aryl-1-triazolyl-2-butanol
Synthesis and Antifungal Activities of Some Thiolane-Triazole Derivatives
Synthesis of Racemic and Optically Active Cispentacin (FR109615) Using Intramolecular Nitrone-Olefin Cycloaddition
A Palladium-Catalyzed, Abnormal Hydrogenolytic Ring-Cleavage Reaction of Fused β-Lactams
β-Lactam Antifungals. II. Enantiocontrolled Synthesis of (2R, 5S)-2-Hydroxymethyl-1-carbapenam, the Carba-Analog of a Clavam Antifungal
Enantiocontrolled Synthesis of the Antifungal β-Lactam (2R, 5S)-2-(Hydroxymethyl)clavam

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