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http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_34/101021ja00139a033/authorship/1
http://hub.abes.fr/acs/periodical/ancham/2001/volume_73/issue_9/101021ac001136i/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_3/101021ja045603f/authorship/3
http://hub.abes.fr/acs/periodical/ancham/2000/volume_72/issue_20/101021ac000356t/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2002/volume_124/issue_32/101021ja0115013/authorship/2
http://hub.abes.fr/acs/periodical/jpcafh/2004/volume_108/issue_4/101021jp0355612/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_11/101021ja0035708/authorship/6
http://hub.abes.fr/acs/periodical/ancham/2001/volume_73/issue_5/101021ac001016a/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1997/volume_119/issue_49/101021ja972892h/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2000/volume_122/issue_49/101021ja002467f/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2000/volume_122/issue_48/101021ja005670j/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_15/101021ja047572u/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1999/volume_121/issue_49/101021ja992511v/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_14/101021jo00249a055/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1990/volume_112/issue_19/101021ja00175a044/authorship/1
http://hub.abes.fr/springer/periodical/10853/1993/volume_28/issue_17/B910822AE9602C51E053120B220A14F3/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1991/volume_113/issue_24/101021ja00024a068/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1993/volume_115/issue_16/101021ja00069a084/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1992/volume_114/issue_26/101021ja00052a086/authorship/2
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Conformation and stereoselective reduction of hapten side chains in the antibody combining site
Selective quinone formation by oxidation of aromatics with heteroaromatic N-oxides catalyzed by ruthenium porphyrins.
Heterolytic oxygen-oxygen bond cleavage of peroxy acid and effective alkane hydroxylation in hydrophobic solvent mediated by an iron porphyrin coordinated by thiolate anion as a model for cytochrome P-450
Synthesis of a highly stable iron porphyrin coordinated by alkylthiolate anion as a model for cytochrome P-450 and its catalytic activity in oxygen-oxygen bond cleavage
Vibronic Coupling between Soret and Higher Energy Excited States in Iron(II) Porphyrins: Raman Excitation Profiles of A2g Modes in the Soret Region
Bioimaging of Nitric Oxide with FluorescentIndicators Based on the Rhodamine Chromophore
Mechanistic Studies on the Binding of Nitric Oxide to aSynthetic Heme−Thiolate Complex Relevant to CytochromeP450
Unique Oxidation Reaction of Amides with Pyridine-N-oxide Catalyzed byRuthenium Porphyrin: Direct Oxidative Conversion of N-Acyl-l-proline toN-Acyl-l-glutamate
Pronounced Axial Thiolate Ligand Effect on theReactivity of High-Valent Oxo−Iron PorphyrinIntermediate
Development of a Time-Resolved FluorometricDetection System Using Diffusion-EnhancedEnergy Transfer
Highly Zinc-Selective Fluorescent Sensor MoleculesSuitable for Biological Applications
Intramolecular Fluorescence Resonance EnergyTransfer System with Coumarin Donor Included inβ-Cyclodextrin
Novel Iron Porphyrin−Alkanethiolate Complex withIntramolecular NH···S Hydrogen Bond: Synthesis,Spectroscopy, and Reactivity
Rational Design of Fluorescein-Based Fluorescence Probes.Mechanism-Based Design of a Maximum Fluorescence Probe forSinglet Oxygen
First Synthetic NO−Heme−Thiolate ComplexRelevant to Nitric Oxide Synthase and CytochromeP450nor
Multiple Active Intermediates in Oxidation Reaction Catalyzedby Synthetic Heme−Thiolate Complex Relevant toCytochrome P450
Study of La1−xMnO3−δ non-stoichiometry and defect structure using ESR and iodometry
Versatile chiral synthons for vic-amino alcohols. Facile synthesis of (2S,3R)-3-hydroxyglutamic acid and (+)-statine
Highly efficient oxidation of alkanes and alkyl alcohols with heteroaromatic N-oxides catalyzed by ruthenium porphyrins
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