稲山誠一 | Pharmaceutical Institute, School of Medicine, Keio University

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著作論文

A Convenient Screening Test for Hypoxic Cell Radiosensitizers/Cytotoxins
Isolation of a Hopane-Type Triterpenoid, Zeorin, from a Higher Plant, Tripterygium regelii
A Rapid and Simple Screening Method for Methamphetamine in Urine by Radioimmunoassay using a ^I-Labeled Methamphetamine Derivative
The Radioimmunoassay for Methamphetamine
Preparation of a Specific Antibody to Methamphetamine
Studies on Radioimmunoassay for Methamphetamine Excreted in Human Urine
The Absolute Configuration of Curcumalactone(Pharmacognosy,Chemical)
A NEW CONVENIENT METHOD FOR MICRODETERMINATION OF HYDROXYPROLINE BY FLOW INJECTION ANALYSIS
Hard Acid and Soft Nucleophile System. VI. A Convenient Synthesis of Alkylthiopolycyclic Aromatics with a Metal Halide and Thiol System
Mass Spectrometry of Oxidation Products of Δ^1-and Δ^6-Tetrahydrocannabinols
The Oxidation of Δ^1-and Δ^6-Tetrahydrocannabinol with Selenium Dioxide
THE ABSOLUTE CONFIGURATION AND CONFORMATION OF NEOCURDIONE
IMMOBILIZATION OF YEAST AND THE FUNCTION OF IMMOBILIZED YEAST
Microbiologically Modified Chiral Synthon. III. 4,9-Dimethyl-3,5-dioxo-Δ^-octalin for Formal Total Syntheses of Certain Sesquiterpenoids
A Series of Sesquiterpenes with a 7α-Isopropyl Side Chain and Related Compounds Isolated from Curcuma wenyujin
MICROBIOLOGICAL ASYMMETRIC INDUCTION OF 4,9-DIMETHYL-3,5-DIOXO-Δ^-OCTALIN
Microbiologically Modified Chiral Synthon. II. : 4,9-Dimethyl-3,7-dioxo-Δ^-octalin for Formal Total Syntheses of Certain C(8) Oxygenated Sesquiterpenoids
Microbiologically Modified Chiral Synthon. I. 3,8-Dioxo-4-methoxycarbonyl-9-methyl-Δ^-octalin for Formal Total Syntheses of Certain Sesquiterpenoids and Diterpenoids
MICROBIOLOGICALLY MODIFIED 4,9-DIMETHYL-Δ^-OCTAL-3,7-DIONES AS THE CHIRAL SYNTHON FOR FORMAL TOTAL SYNTHESES OF C(8) OXYGENATED SESQUITERPENOIDS(Communications to the Editor)
MICROBIOLOGICAL ASYMMETRIC REDUCTION OF 4-CARBOMETHOXY-3,8-DIOXO-9-METHYL-Δ^-OCTALIN
Studies on Non-sesquiterpenoid Constituents of Gaillardia pulchella. II. Less Lipophilic Substances, Methyl Caffeate as an Antitumor Catecholic
Ambrosic Acid, a New Irritant Principle from Ambrosia arthemisiifolia
The Absolute Structure and Synthesis of Wenjine Isolated from Curcuma wenyujin
The Diels-Alder Reaction of 3-Acetoxy-1-vinylcyclohexene with Methyl Vinyl Ketone
THE STEREOSTRUCTURE OF WENJINE AND RELATED (1S__-, 10S__-), (4S__-, 5S__-)-GERMACRONE-1(10), 4-DIEPOXIDE ISOLATED FROM CURCUMA WENYUJIN
THE ABSOLUTE CONFIGURATION OF REGELIDINE, A NOVEL 6-NICOTINOYL DIHYDROAGAROFURAN SESQUITERPENE ALKALOID FROM TRIPTERYGIUM REGELII(Communications to the Editor)
ISOLATION AND STRUCTURE OF REGELIN AND REGELINOL, NEW ANTITUMOR URSENE-TYPE TRITERPENOIDS FROM TRIPTERYGIUM REGELII(Communication to the Editor)
A NOTE ON THE A-RING CONFORMATION IN 2-CHLORO-1,2-DIHYDROSANTONINS
CONFORMATION OF CHLORODIHYDROSANTONINS
Preparation, Decarboxylation and Absolute Configuration of (+)-11α-Carboxy- and (+)-11β-Carboxy-3α, 4β, 5α, 6βH-hexahydrosantonin, and (-)-11β-Carboxysantonin
A New Helenanolide, 11βH-Dihydro-4-epineopulchellin, Isolated from Gaillardia grandiflora
THE ABSOLUTE CONFIGURATION OF CURDIONE AND THE STEREOSTRUCTURE OF CURCUMALACTONE FROM CURCUMA WENYUJIN
STEREOSTRUCTURE OF CURDIONE
THE ABSOLUTE STEREOSTRUCTURE OF CURCUMOL ISOLATED FROM CUROCUMA WENYUJIN
Studies on New Synthetic Pathways to ⊿^-butenolides from α-Methylbutanolides. III. Regiospecific Preparation of α-Methyl-⊿^-butenolides and α-Methylene-γ-butyrolactones by Electrolysis of α-Carboxy-α-methylbutanolides and by Oxidat
Studies on New Synthetic Pathways to ⊿^-Butenolides from a-Methylbutanolides. II. Electrolytic Oxidation of Simple a-Carboxy-a-methylbutanolides
A New Synthetic Pathway to Δ^-Butenolide from γ-Butyrolactone
A Michael Addition of Amines to α-Methylene-γ-butyrolactones

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