渋谷博孝 | Faculty of Pharmaceutical Sciences, Osaka University

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著作論文

STRUCTURE OF THEONELLAPEPTOLIDE ID, A NEW BIOACTIVE PEPTOLIDE FROM AN OKIKAWAN MARINE SPONGE, THEONELLA SP. (THEONELLIAE)
Chemical Transformation of Terpenoids. X. Ionophoretic Activities of Macrocyclic Lactone Epoxides Synthesized from Geraniol
Syntheses of a Glycerophospholipid, C16-Platelet Activating Factor and a Palmitoyl Analogue of M-5,an Anti-inflammatory Glyceroglycolipid
Syntheses of Two Pairs of Enantiomeric C18-Sphingosines and a Palmitoyl Analogue of Gaucher Spleen Glucocerebroside
Indonesian Medicinal Plants. XI. Chemical Structures of Caesaldekarins a and b, Two New Cassane-Type Furanoditerpenes from the Roots of Caesalpinia major (Fabaceae)
A NEW METHOD FOR MEASURING IONOPHORETIC ACTIVITY USING A GLASS-CELL APPARATUS EQUIPPED WITH ARTIFICIAL MEMBRANES
Indonesian Medicinal Plants. X. Chemical Structures of Four New Triterpene-Glycosides, Gongganosides D, E, F, and G, and Two Secoiridoid-Glucosides from the Bark of Bhesa paniculata (Celastraceae)
Indonesian Medicinal Plants. IX. Chemical Structures of Gongganosides A, B, and C, Three New Quinovic Acid Glycosides from the Bark of Bhesa paniculata (Celastraceae)
Chemical Transformation of Terpenoids. VI. Syntheses of Chiral Segments, Key Building-Blocks for the Left Half of Taxane-Type Diterpenoids
Chemical Transformation of Terpenoids. IV. Acid Treatment of (3R)-1-Vinyl-, (3R)-1-Hydroxypropenyl-, and (3R)-1-Epoxyethyl-5-methoxy-1,2,2-trimethylcyclopentane Derivatives : Ring Enlargement Reactions and Successive Migrations of Methyl Residues
Chemical Transformation of Terpenoids. III. Syntheses of (3R)-1-Vinyl-, (3R)-1-Hydroxypropenyl-, and (3R)-1-Epoxyethyl-5-methoxy-1,2,2-trimethylcyclopentane Derivatives from d-Camphor via 5-Oxo-d-bornyl Acetate
Chemical Transformation of Terpenoids. II. Acid Treatment of (3S)-1-Vinyl-, (3S)-1-Hydroxypropenyl-, and (3S)-1-Epoxyethyl-1,2,2-trimethylcyclopentane Derivatives : Ring Enlargement Reactions and Successive Migrations of Methyl Residues
Chemical Transformation of Terpenoids. I. Syntheses of (3S)-1-Vinyl-, (3S)-1-Hydroxypropenyl-, and (3S)-1-Epoxyethyl-1,2,2-trimethylcyclopentane Derivatives from d-Camphor via d-Camphoric Acid
Biogenetically Patterned Transformation of Eudesmanolide to Eremophilanolide. V. Studies on Stereochemical Factors for Favorable Conversion of 5α, 6α-Epoxy-eudesman-8β, 12-olide leading to Eremophilane-type Derivatives
Studies on the chemical Modification of Monensin. III. Synthesis and Sodium Ion transport Activity of macrocylic Monenslamino Acid-1,29-lactones
DEHATRINE, AN ANTIMALARIAL BISBENZYLISOQUINOLINE ALKALOID FROM THE INDONESIAN MEDICINAL PLANT BEILSCHMIEDIA MADANG, ISOLATED AS A MIXTURE OF TWO ROTATIONAL ISOMERS
Indonesian Medicinal Plants. V. Chemical Structures of Calotroposides C, D, E, F, and G, Five Additional New Oxypregnane-Oligoglycosides from the Root of Calotropis gigantea (Asclepiadaceae)
Indonesian Medicinal Plants. IV. On the Constituents of the Bark of Fagara rhetza (Rutaceae). (2). Lignan Glycosides and Two Apioglucosides
Indonesian Medicinal Plants. III. On the Constituents of the Bark of Fagara rhetza (Rutaceae).(1) : Alkaloids, Phenylpropanoids, and Acid Amide
Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae)
Marine Natural Products. XXVI. Biologically Active Tridecapeptide Lactones from the Okinawan Marine Sponge Theonella swinhoei(Theonellidae).(2).Structures of Theonellapeptolides Ia, Ib, Ic, and Ie
Sphingolipids and Glycerolipids. I. : Chemical Structures and Ionophoretic Activities of Soyacerebrosides I and II from Soybean
MAMMOSIDES B AND H1,NEW IONOPHORIC RESIN-GLYCOSIDES FROM THE TUBER OF MERREMIA MAMMOSA, AN INDONESIAN FOLK MEDICINE
Sphingolipids and Glycerolipids. IV. Syntheses and Ionophoretic Activities of Several Analogues of Soya-cerebroside II, a Calcium Ionophoretic Sphingoglycolipid Isolated from Soybean
Chemical Transformation of Terpenoids. VIII. Anodic Oxidation of Geranyl Acetate
IONOPHORETIC ACTIVITIES OF OLIGOPEPTIDE LACTONES AND RESIN-GLYCOSIDES IN HUMAN ERYTHEROCYTES
Biogenetically Patterned Transformation of Eudesmanolide to Eremophilanolide. I. Angular Methyl Migration of 5α, 6α-Epoxy-dihydroalantolactone
PULOSARIOSIDE, A NEW BITTER TRIMERIC-IRIDOID DIGLUCOSIDE, FROM AN INDONESIAN JAMU : THE BARK OF ALYXIA REINWARDTII BL__=. : APOCYNACEAE
STRUCTURES OF MERREMOSIDES B AND D, NEW ANTISEROTONIC RESIN-GLYCOSIDES FROM THE TUBER OF MERREMIA MAMMOSA, AN INDONESIAN FOLK MEDICINE
Chemical Transformation of Terpenoids. VII. Syntheses of Chiral Segments, Key Building-Blocks for the Right Half of Taxane-Type Diterpenoids
TAXOL AND ITS RELATED TAXOIDS FROM THE NEEDLES OF TAXUS SUMATRANA
Indonesian Medicinal Plants. VIII. Chemical Structures of Three New Triterpenoids, Bruceajavanin A, Dihydrobruceajavanin A, and Bruceajavanin B, and a New Alkaloidal Glycoside, Bruceacanthinoside, from the Stems of Brucea javanica (Simaroubaceae)
Indonesian Medicinal Plants. VII. Seven New Clerodane-Type Diterpenoids, Peronemins A_2,A_3,B_1,B_2,B_3,C_1,and D_1,from the Leaves of Peronema canescens (Verbenaceae)
Biogenetically Patterned Transformation of Eudesmanolide to Eremophilanolide. IV. Conversion of Alantolactone to Several Furanoeremophilane Derivatives
STRUCTURE OF THEONELLAPEPTOLIDE IE, A NEW TRIDECAPEPTIDE LACTONE FROM AN OKINAWAN MARINE SPONGE, THEONELLA SP. (THEONELLIDAE)(Communication to the Editor)
Biogenetically Patterned Transformation of Eudesmanolide to Eremo-philanolide. II. Structures of Minor Products obtained by Acid Treatment of 5α, 6α-Epoxy-eudesman-8β, 12-olide
Biogenetically Patterned Transformation of Eudesmanolide to Eremophilanolide. III. Acid Treatment of 4α, 5α-Epoxy-eudesman-8β, 12-olide
THE ABSOLUTE STEREOSTRUCTURE OF (4S, 5S)-(+)-GERMACRONE 4,5-EPOXIDE FROM ZEDOARIAE RHIZOMA CULTIVATED IN YAKUSHIMA ISLAND
CHEMICAL CONVERSION OF (4S, 5S)-(+)-GERMACRONE 4,5-EPOXIDE, A PLAUSIBLE BIOGENETIC INTERMEDIATE FOUND IN THE ESSENTIAL OIL OF ZEDOARIAE RHIZOMA FROM YAKUSHIMA, JAPAN
Chemical Transformation of Terpenoids. V. Acidic Conversions of 10-Hydroxygeraniol and 10-Hydroxynerol Derivatives Leading to Cyclic Monoterpenoids
A REINVESTIGATION OF THE STRUCTURE OF ZEDERONE, A FURANOGERMACRANE-TYPE SESQUITERPENE FROM ZEDOARY(Communications to the Editor)
Oxygen-Functionalization of C_-Angular Methyl Group in Pregnane Steroid by Means of Intramolecular Carbonyl-Mediated Anodic Oxidation

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