Sato Ken-ichi | Laboratory of Chemistry for Natural Products, Faculty of Science, Tokyo Institute of Technology

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著作論文

Hydrogen peroxide induces Src family tyrosine kinase-dependent activation of Xenopus eggs
Crystal Structure of(1R, 2R, 3S, 4S, 5S, 6S, 7R, 9S)-6-Azido-7-cyano-3-C-hydroxy-methyl-3, 3'-di-O-isopropylidene-9-methoxy-2, 4, 5-tris(O-methoxymethyl)-2, 3, 4, 5-tetrahydroxy-8-oxabicyclo[4. 3. 0]nonane, toward Tetrodotoxin
Convenient Syntheses of 3-Deoxy-D-manno-2-octulosonic Acid (KDO) and 3-Deoxy-D-glycero-D-galacto-2-nonulosonic Acid (KDN) Derivatives from D-Mannose
Total Syntheses of Bistratamides J, E, and H from Two Types of ΔAla-Containing Oligopeptides
Useful Intermediates, 3-C-Dichloromethyl Furanose Derivatives, for the Synthesis of Branched-Chain Functionalized Sugars
Crystal Structure of Potential Key Compounds, DL-(1, 2, 3', 4, 5, 6'/3, 6)-6-Azido-5'-O-t-butyldiphenylsilyl-6-(cyano)hydroxymethyl-3, 5-di-C-hydroxymethyl-1, 2 : 3, 3'-di-O-isopropylidene-4-O-methoxymethyl-1, 2, 3, 4-cyclohexanetetrol, toward(±)-Tetrodot
An Efficient Deoxysugar Synthesis using Bu4NBH4 via an SN2 Reduction
Total Synthesis of a Novel β-Glucosidase Inhibitor, Cyclophellitol Starting from D-Glucose
Reaction of α-Hydroxydichloromethyl Derivatives with Cesium Acetate
A Novel Method for Constructions of β-D-Mannosidic, 2-Acetamido-2-deoxy-β-D-mannosidic, and 2-Deoxy-β-D-arabino-hexopyranosidic Units from the Bis(triflate) Derivative of β-D-Galactoside
A Novel Method for Constructing β-D-Mannosidic, 2-Acetamido-2-deoxy-β-D-mannosidic, and 2-Deoxy-D-arabino-hexopyranosidic Units from the Bis(triflate) Derivative of β-D-Galactoside
Branched-chain Sugars. XXIX. Synthesis of Moenuronic Acid (4-C-Methyl-D-glucuronic Acid)
Branched-chain Sugars. IX. Reaction of 3,6-Anhydro-1,2-O-isopropylidene-α-D-ribo-hexofuranos-3-ulose with Nitromethane or Hydrogen Cyanide
Branched-chain Sugars. VIII. On the Configuration of Branched-chain Sugars from Methyl 3-O-Benzoyl-4,6-O-benzylidene-α-D-arabino-hexopyranosid-2-ulose
Branched-chain Sugars. XXIII. Stereoselectivities in the Addition of Nucleophiles to Several 4-Uloses
Branched-chain Sugars. XX. Kinetic Studies on the Epimerization of 1,2 : 5,6-Di-O-isopropylidene-3-C-nitromethyl-α-D-allofuranose
α,β-Unsaturated Carboxylic Acid Derivatives. IV. General Synthesis of Unsaturated Unsymmetric 3,6-Disubstituted-2,5-piperazinediones
Aminosugars. XXVIII. A Facile Synthesis of Benzyl α- and β-Kasugaminides via the Corresponding Abequosides
Branched-chain Sugars. XII. The Stereoselectivities in the Reaction of Methyl 4,6-O-Benzylidene-α- and -β-D-hexopyranosid-3-uloses with Diazomethane
Synthesis of 2,2-Di-C-methyl-2-deoxy- and 4,4-Di-C-methyl-4-deoxypyranosides via Michael Addition of Conjugated Enopyranosiduloses
Branched-chain Sugars. XIX. On the Application of 13C NMR Spectroscopy to the Configurational Assignment of 3-C-Substituents of Aldohexopyranose Derivatives
Branched-Chain Sugars. II. On the Configuration of Branched-Chain Sugars from Methyl 2-O-Benzoyl-4,6-O-benzylidene-α-D-ribo-hexopyranosid-3-ulose

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