TOSHIMA Hiroaki | Department of Bioresource Science, College of Agriculture, Ibaraki University

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概要

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著作論文

Cloning of a Gene Cluster Responsible for the Biosynthesis of Diterpene Aphidicolin, a Specific Inhibitor of DNA Polymerase α
Wound-Induced Expression of a Tobacco Peroxidase Is Not Enhanced by Ethephon and Suppressed by Methyl Jasmonate and Coronatine
Diterpene Cyclases Responsible for the Biosynthesis of Phytoalexins, Momilactones A, B, and Oryzalexins A-F in Rice
Syntheses and Potato Tuber-inducing Activity of Coronafacic Acid Analogues
Efficient Syntheses of the OPC Homologous Series, OPC-1:0, -3:0, -4:0, -5:0, -6:0, -7:0, and -8:0
Asymmetric Total Syntheses of (+)-Coronafacic Acid and (+)-Coronatine
Cloning of the Gene Cluster Responsible for the Biosynthesis of Brasilicardin A, a Unique Diterpenoid
Characterization of a Rice Gene Family Encoding Type-A Diterpene Cyclases
Total Syntheses of All Four Stereoisomers of Piscidic Acid via Catalytic Asymmetric Dihydroxylation of (Z)- and (E)-trisubstituted Olefins
Total Synthesis of (+)-(2S, 3R)-Piscidic Acid via Catalytic Asymmetric Dihydroxylation of a Trisubstituted Olefin
(-)-Semivioxanthin, A New Abscisic Active Compound against Hinoki Cypress Leaves Isolated from Cryptosporiopsis abietina
Identification of Diterpene Biosynthetic Gene Clusters and Functional Analysis of Labdane-Related Diterpene Cyclases in Phomopsis amygdali
Total Synthesis of (±) -syn-Copalol(Organic Chemistry)
P-99 SOLID-PHASE SYNTHESIS OF DEHYDROPEPTIDES
Syntheses and Potato Tuber-inducing Activities of Unnatural Long-chain OPC-9 : 0 and OPC-10 : 0
Syntheses of 3-Oxa-OPC and 2-Fluoro-OPC Homologues
Inhibitory Effect of Coronamic Acid Derivatives on Senescence in Cut Carnation Flowers
Practical Stereoselective Syntheses of All Four Stereoisomers of Coronamic Acid (2-Ethyl-1-aminocyclopropane-1-carboxylic acid)
Identification of Diterpene. Biosynthetic Gene Clusters and Functional Analysis of Labdane-Related Diterpene Cyclases in Phomopsis amygdali
Improved Synthesis of the C_8-C_ Segment of Aplysiatoxins via Asymmetric Dihydroxylation of the Chiral Homoallylic Alcohol
Total Synthesis of Biologically Active Compounds Related to Plant Disease and the Physiological Function
Stereoselective Synthesis of a Promising Flower-Inducing KODA Analog, (9R,12S,13R,15Z)-9-Hydroxy-12,13-methylene-10-oxooctadec-15-enoic Acid

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