KINDAI UNIVERSITY


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YAMAGUCHI Yoshihiro

Profile

FacultyDepartment of Science / Graduate School of Science and Engineering Research
PositionProfessor
Degree
Commentator Guidehttps://www.kindai.ac.jp/meikan/340-yamaguchi-yoshihiro.html
URL
Mail
Last Updated :2020/04/03

Education and Career

Education

  •  - 1987 , Tohoku University
  •  - 1987 , Tohoku University, Graduate School, Division of Natural Science
  •  - 1981 , Tohoku University, Faculty of Science
  •  - 1981 , Tohoku University, Faculty of Science

Research Activities

Research Areas

  • Manufacturing technology (mechanical, electrical/electronic, chemical engineering), Electronic devices and equipment
  • Nanotechnology/Materials, Functional solid-state chemistry
  • Life sciences, Bioorganic chemistry
  • Nanotechnology/Materials, Structural/physical organic chemistry

Published Papers

  • Highly Emissive Whole Rainbow Fluorophores Consisting of 1,​4-​Bis(2-​phenylethynyl)​benzene Core Skeleton: Design, Synthesis, and Light-​Emitting Characteristics, YAMAGUCHI Yoshihiro, Journal of Physical Chemistry A, Journal of Physical Chemistry A, 119(32), 8630 - 8642, 2015 , Refereed
  • Assembly of Substituted 2-Alkylquinolines by a Sequential Palladium-Catalyzed C-N and C-C Bond Formation, Angewandte Chemie International Edition, Angewandte Chemie International Edition, 50(33), 7670 - 7673, Aug. 2011
    Summary:A range of substituted 2-alkylquinolines can be prepared in a general and efficient synthetic approach that employs mild reaction conditions. The synthesis is based on a sequentional palladium-catalyzed C-N and C-C bond formation, followed by palladium-catalyzed aromatization, and results in the formation of the desired compounds in one step.
  • Analytical study of interaction between spdider toxin and glutamate receptors., Peptide Science 2009, Peptide Science 2009, 349 - 352, 2010
  • Highly fluorescent oligomers with donor and acceptor groups: DFT calculations and experiments, Synthetic Metals, Synthetic Metals, 159(21-22), 2211 - 2214, Nov. 2009
  • Syntheses of NPTX-594 Analogs with Thiol-Containing Fluorophores to Develop a Probe for Analysis of Binding Mode between Spider Toxins and Glutamate Receptors, Protein & Peptide Letters, Protein & Peptide Letters, 16(3), Mar. 2009
    Summary:NPTX-594 is a neurotoxic acylpolyamine isolated from a Madagascar Joro spider, and seems to act as a specific blocker like general spider toxins against glutamate receptors (GluRs). The present study reports the creation of novel NPTX-594 analogs with thiol-containing fluorophores to adopt as visualization probes for the analysis of binding mode between spider toxins and GluRs, and the result of their cricket bioassay.
  • Syntheses and Biological Activities of Fluorescent-Labeled Analogs of Acylpolyamine Toxin NPTX-594 Isolated from the Venom of Madagascar Joro Spider, Bioorganic & Medicinal Chemistry, Bioorganic & Medicinal Chemistry, 17(1), 57 - 63, Jan. 2009
    Summary:Acylpolyamine-type spider toxins are known to be potent and specific blockers against glutamate receptors (GluRs). The present study descirbes the syntheses and biological activities of several fluorescent-labeled analogs related to a Madagascar Joro spider toxin NPTX-594 to analyze visually the unknown interaction between spider toxins and GluRs.
  • Meso-Disubstituted Anthracenes with Fluorine-Containing Groups: Synthesis, Light-Emitting Characteristics and Photostability, Organic Letters, Organic Letters, 10(24), 5541 - 5544, Dec. 2008
  • How the π Conjugation Length Affects the Fluorescence Emission Efficiency, Journal of the American Chemical Society, Journal of the American Chemical Society, 130(42), 13867 - 13869, Oct. 2008
  • Development of the first and practical method for enantioselective synthesis of 10B-enriched p-borono-L-phenylalanine, Tetrahedron Letters, Tetrahedron Letters, 49(33), 4977 - 4980, Aug. 2008
    Summary:At present <I>p</I>-(<SUP>10</SUP>B)borono-L-phenylalanine (L-<SUP>10</SUP>Bpa) is used clinically as an excellent 10B carrier for BNCT, however its enantioselective synthesis has not been reported yet. The present paper describes the first and practical method for enantioselective synthesis of <SUP>10</SUP>B-enriched L-Bpa using Z-L-Ser-OMe as the chiral synthon in good total yield and high optical purity.
  • Photophysical Properties of Oligophenyleneethynylenes Modified by Donor and/or Acceptor Groups., Journal Physical Chemistry A, Journal Physical Chemistry A, 112(23), 5074 - 5084, Jun. 2008
  • Block Modification of Rod-Shaped pi Conjugated Carbon Framework with Donor and Acceptor Groups Toward Highly Fluorescent Molecules: Synthesis and Emission Characteristics, Organic & Biomolecular Chemistry, Organic & Biomolecular Chemistry, 6(7), 1222 - 1231, Mar. 2008
  • Study directed toward the analysis of interaction between the spider toxin NPTX-594 and glutamate receptors., Peptide Science, Peptide Science, 2008, 401 - 404, 2008
  • Rod-shaped Oligophenylene Ethynylenes Modified by Donor and Acceptor Groups in a Block Manner: Synthesis and Light-emitting Characteristics, Chemistry Letters, Chemistry Letters, 36(6), 794 - 795, Jun. 2007
  • Analysis of bile acid glutathione thioesters by liquid chromatography/electrospray ionization-tandem mass spectrometry, Journal of Chromatography B, Journal of Chromatography B, 855, 88 - 97, Feb. 2007
  • Synthesis and evaluation as MRI probe of the trifluoromethylated p-boronophenylalanine and its alcohol derivative., Bioorganic and Medicinal Chemistry, Bioorganic and Medicinal Chemistry, 15(5), 2298 - 2302, Jan. 2007
  • Biological evaluation of fluorinated p-boronophenylalanine derivatives as boron carrier, Protein and Peptide Letters, Protein and Peptide Letters, 15(3), 269 - 272, Jan. 2007
  • Rigid Molecular Architectures That Comprise a 1,3,5-Tri-Substituted Benzene Core and Three Oligoaryleneethynylene Arms: Light-Emitting Characteristics and pi Conjugation between The Arms, Journal of The American Chemical Society, Journal of The American Chemical Society, 128(14), 4504 - 4505, Apr. 2006
  • Study on the compounds containing 19F and 10B atoms in a single molecule for the application to MRI and BNCT, Bioorganic & Medicinal Chemistry, Bioorganic & Medicinal Chemistry, 14, 3258 - 3262, Feb. 2006
  • New Fluorophores with Rod-Shaped Polycyano-p Conjugated Structures: Synthesis and Photophysical Properties., Organic Letters, Organic Letters, 8(4), 717 - 720, Feb. 2006
  • Synthtic Study of a Cardiac Steroid, Marinoic Acid, J. School Sci. Eng. Kinki Univ., J. School Sci. Eng. Kinki Univ., (41), 17 - 22, Sep. 2005
  • Structural determination of novel acylpolyamines from the venom of Nephila clavipes , a Brajilian spider, Journal of The School of Science and Engineering Kinki University, Journal of The School of Science and Engineering Kinki University, 41, 23 - 29, Sep. 2005
  • Synthetic study of fluorine containing peptides to use for diagnosis of cancer, Journal of the School of Science and Engineering Kinki University, Journal of the School of Science and Engineering Kinki University, 31 - 35, Sep. 2005
  • Study on the solid-phase synthesis of cuclic peptides containing asparagine or glutamine, 169 - 172, Apr. 2003
  • Study on solid-phase synthesis of compounds, containing hydroxyamino acids or saccharides, by taking advantage of the characteristics of glutamic acid, 316 - 317, Apr. 2003
  • Study on peptides inhibiting the activation of gelatinase A (MMP 2), 227 - 230, Mar. 2002

Books etc

  • Invention of Conjugated Electronic Structures: Synthesis, Functions and Applications, Creation of Oligo(phenyleneethynylene)-type Fluorophores, 共著,   2008 01
  • Peptides 2006, Synthesis and in vitro evaluation of fluorinated p-boronophenylalanine derivatives as boron carrier and MRI probe, 共著, Kenes International,   2007 07
  • Peptides 2006, Electron transfer of flat peptides, 共著, Kenes International,   2007 07
  • Peptides 2006, Studies on the syntheses and LC/ESI-MS analyses of the glutathione conjugates of bile acids, 共著, Kenes International,   2007 07
  • Peptide Science 2006, Syntheses and Biological Activities of Fluorescent Labeled Analogs of Acylpolyaminetoxin, 共著,   2006 11
  • Peptide Science 2006, Study on the syntheses and LC/ESI-MSn analyses of glutathione conjugates of bile acids, 共著,   2006 11
  • Peptide Science 2006, In vitro and vivo evaluation of fluorinated p-boronophenylalanine derivatives as boron carrier and MRI probe, 共著,   2006 11
  • Peptide Science 2005, Study on the structure activity rerationship of a phytosiderophore, mugineic acid, 共著,   2006 03
  • Peptide Science 2005, Synthesis and biological activity of fluorescent labeled analogs of the spider toxin NPTX-594, 共著,   2006 03
  • Peptide Science 2005, Synthesis and evaluation of the compounds containing 10B and 19F atoms as boron carrier and imaging agent, 共著,   2006 03
  • Peptide Science 2005, Syntheses and 3D-structual analyses of α,β-dehydroalanine- and α,β-dehydrovaline-homopeptides, 共著,   2006 03
  • Peptide Science 2004 , Structural study of novel acylpolyaminetoxins from the venom of Nephila clavipes , a Brajilian spider, 共著, The Japanese Peptide Society,   2005 04
  • Peptide Science 2004 , Study of the fluorine- and boron-10 containing compounds toward MRI and BNCT, 共著, The Japanese Peptide Society,   2005 04
  • Peptides 2004, Study on fluoline- and/or boron-containing amino acids and their related compounds as tools for diagnosis and treatment of cancer, 共著, Kenes International,   2005 03
  • Study on suructure activity relationships of spider toxins with a generalized acylpolyamine structure of type B, 共著,   2001 04

Conference Activities & Talks

  • Synthesis and Photophysical Properties of Organic Luminophores Bearing 1, 2, 3-Triazole Rings,   2011 03
  • Synthesis and Luminescent Characteristics of Aromatic Cyclic Boron Complexes Having N-B-N Bond,   2011 03
  • Synthesis and Light-emitting Characteristics of Donor/Acceptor Type Oligo(phenyleneethnylene)s Having Acceptor Unit at The Both Molecular End,   2011 03
  • Synthesis of Oraganic Fluorophores Having Condensed Coumarin Rings,   2011 03
  • Synthesis of organic luminophores having 1,2,3-triazole rings,   2010 03
  • Two-photon absorption characteristics of star-shaped donor/acceptor type fluorophores having nitrogen atom at the molecular center,   2010 03
  • Synthesis and photophysical properties of novel perylene derivatives,   2010 03
  • Light-emitting characteristics of Zn(II) complex of oligo(phenyleneethnylene)s having terpyridine groups at the terminal,   2010 03
  • Synthesis and light-emitting characteristics of donor/acceptor type oligo(phenyleneethnylene)s having terphenyl groups at the terminal,   2010 03
  • Synthesis and photophysical properties of novel N-containing p-conjugated ring systems,   2010 03
  • Synthesis and light-emitting characteristics of donor/acceptor type of phenylethnyl-substituted anthracenes,   2010 03
  • Synthesis and luminescent characteristics of boron complexes of aromatics having bidentate nitrogen ligands,   2010 03
  • Light-Emitting Characteristics in Solid State of Donor/Acceptor Type Oligo(phenyleneethnylene)s Having Acceptor Unit at The Molecular Center,   2009 03
  • Synthesis and Light-Emitting Properties of Donor/Acceptor Type Phenyleneethynylene-Dendrimer,   2009 03
  • Synthesis and Light-Emitting Properties of p,p’-Disubstituted Diphenylacetylenes and Their Derivatives,   2009 03
  • Synthesis and Light-Emitting Characteristics of p-Diethynylbenzenes Having m-Terphenyl Groups at Both Ends of The Molecules,   2009 03
  • Synthesis and Light-Emitting Characteristics of Star-Shaped Donor/Acceptor Type Fluorophores Having Nitrogen Atom at The Center of Molecule,   2009 03
  • The Change of Light-Emitting Characteristics by The Array Control of Donor and Acceptor Units in Donor/Acceptor Type Oligo(phenyleneethynylene)s,   2009 03
  • Highly Fluorescent Oligophenylene Ethynylenes with Donor and AcceptorGroups: Theoretical calculations and experiments, 18th IKETANI CONFERENCE,   2008 10 , 18th IKETANI CONFERENCE
  • Synthesis of spider toxin NPTX-594 analogs with the alkyne group for post fluorescent labeling,   2008 10
    Summary:Acylpolyamine toxins in spider venom are known to be potent and specific blockers against glutamate receptors (GluRs) in the mammalian central nervous systems or in the arthropod ganglia. In order to elucidate the specific binding of spider toxins to GluRs, the present study describes the syntheses of spider toxin NPTX-594 analogs with the alkyne group that is convertible into fluorescent moiety based on the reaction with azide-containing fluorophores by means of click chemistry.
  • Creation of novel spider toxin analogs to adopt as probes for visualization of glutamate receptors, 30th European Peptide Symposium,   2008 09 , 30th European Peptide Symposium
  • Enantioselective synthesis of fluorinated p-borono-L-phenylalanines enriched with 10B atom, 30th European Peptide Symposium,   2008 09 , 30th European Peptide Symposium
  • Opto-electronics materials derived from novel pi-conjugated systems., The 8th International Symposium on Functional pi-Electron Systems,   2008 07 , The 8th International Symposium on Functional pi-Electron Systems
  • Highly Fluorescent Oligomers with Donor and Acceptor Groups: DFT Calculations and Experiments, International Conference on the Science and Technology of Synthetic Metals (ICSM2008),   2008 07 , International Conference on the Science and Technology of Synthetic Metals (ICSM2008)
  • Synthesis of Rod-shaped Red Oligo(phenyleneethynylene)-fluorophores Modified by CN and HexO Groups in a Block Manner.,   2008 03
  • Synthesis of Dendritic Red Fluorophores,   2008 03
  • Photophisical Properties of Rod-shaped Oligo(phenyleneethynylene)s Modified by Donor and Acceptor Groups in a Block Manner,   2008 03
  • Creation of Intense Red Fluorophores That Comprise Donor-Substituted Polycyano-pi Conjugated Systems.,   2008 03
  • Synthesis and Light-emitting Properties of Perylene Derivatives Containing Heterocyclic Rings.,   2008 03
  • Synthesis and Light-emitting Properties of Oligo(phenyleneethynylene)s Containing Disilyl Groups.,   2008 03
  • Relationship of pi Conjugation Length with the Fluorescence Emission Efficiency,   2008 03
  • Creation of Novel Spider Toxin Analogs Using as Probes for Visualization of Glutamate Receptor,   2008 03
  • Synthesis of Expanded Cubane-type Molecules Composed by p-Azaarylene Rings.,   2008 03
  • Synthesis of Rod-shaped Oligo(phenyleneethynylene)-fluorophores Modified by CN and Me2N Groups in a Block Manner.,   2008 03
  • Synthesis of a phophopeptide thioester with difficult sequence,   2007 12
  • Synthesis of Dendritic Red Fluorophores,   2007 11
  • Synthesis and Chemical Properties of p-azaarylenecyclyne Dimer,   2007 11
  • Synthesis of optically active β-[4-(10B)borono-2,6-difluorophenyl]alanine and its evaluation as a boron carrier of BNCT,   2007 11
  • Synthesis of Rod-shaped Red Fluorophores,   2007 11
  • Donor and Acceptor-Substituted Oligo(phenyleneethynylene)s Having The Acceptor Groups at The Molecular Center: Synthesis and Light-Emitting Characteristics,   2007 03
  • Synthesis of azaarylene-macrocycles.,   2007 03
  • Light-Emitting Characteristics of Rod-Shaped Polymethoxy-Oligo(phenyleneethynylene)s Having Electron-Withdrawing Groups at The Molecular End.,   2007 03
  • Block Modification of Rod-Shaped π Conjugated Systems with Donor and Acceptor Groups: Synthesis and Light-Emitting Characteristics.,   2007 03
  • Synthesis and Light-emitting Characteristics of Rod-Shaped π-Conjugated Systems Containig Bipyridine Unit,   2007 03
  • Synthesis and Light-emitting Properties of Novel Organic Luminophors That Comprise Benzofuran Rings.,   2007 03
  • Creation of A Whole Rainbow of Fluorophores and Chromophores by Construction of Donor-Substituted Polycyano-p Conjugated Systems.,   2007 03
  • Synthesis and Light-emitting Characteristics of π Conjugated Systems Containing Bithiophene or Bipyridine,   2006 12
  • Synthesis and Light-emitting Characteristics of Novel Organic Light-emitter.,   2006 12
  • Synthetic studies of p-azaarylenecyclynes and their dimer.,   2006 12
  • Syntheses and Biological Activities of Fluorescent Labeled Analogs of AcylpolyaminetoxinNPTX-594 Isolated from the Venom of Madagascar Joro Spider,   2006 12
  • Block Modification of Rod-Shaped p Conjugated Carbon Framework with Donor and Acceptor Groups: Synthesis and Light-Emitting Characteristics., The Fifth International Forum on Chemistry of Functional Organic Chemicals,   2006 11 , The Fifth International Forum on Chemistry of Functional Organic Chemicals
  • Syntheses and Biological Activities of Fluorescent Labeled Analogs of Acylpolyaminetoxin,   2006 11
  • Study on the syntheses and LC/ESI-MSn analyses of the glutathione conjugates of bile acids,   2006 11
  • Novel Light-Emitters with Rod-Shaped Polycyano-π Conjugated Structures: Creation of A Whole Rainbow of Fluorophores., The Fifth International Forum on Chemistry of Functional Organic Chemicals (IFOC-5),   2006 11 , The Fifth International Forum on Chemistry of Functional Organic Chemicals (IFOC-5)
  • Star-shaped Oligophenyleneethynylene Architectures: Synthesis, Light-Emitting Characteristics, and π Conjugation between the Arms., The Fifth International Forum on Chemistry of Functional Organic Chemicals (IFOC-5),   2006 11 , The Fifth International Forum on Chemistry of Functional Organic Chemicals (IFOC-5)
  • In vitro and vivo evaluation of fluorinated p-boronophenylalanine derivatives as boron carrier and MRI probe,   2006 11
  • Synthesis and biological evaluation of fluorinated p-boronophenylalanine derivatives, 12th International Congress on Neutron Capture Therapy,   2006 10 , 12th International Congress on Neutron Capture Therapy
  • Synthesis and in vitro evaluation of fluorinated p-boronophenylalanine derivatives as boron carrier and MRI probe,   2006 09
  • Electron transfer to flat peptides,   2006 09
  • Study on the syntheses and LC/ESI-MS analyses of the glutathione conjugates of bile acids,   2006 09
  • New Fluorophores with Rod-shaped Polycyano pi conjugated Structures: Synthesis and Light-emitting Characteristics., The Seventh International Symposium on Functional pi-Electron Systems,   2006 05 , The Seventh International Symposium on Functional pi-Electron Systems
  • Star-shaped Oligophenyleneethynylene Architectures: Synthesis and Photophysical Properties., The Seventh International Symposium on Functional pi-Electron Systems,   2006 05 , The Seventh International Symposium on Functional pi-Electron Systems
  • Enzymatic transformation of bile acids into glutathione conjugates,   2006 03
  • Synthesis and Light-emitting Characteristics of Polycyano pi-conjugated systems.,   2006 03
  • Synthesis of the cubric type dimeric system of azaaryleneethynylene.,   2006 03
  • Synthesis and Light-emitting Characteristics of Donor-Acceptor Type Oligo(fluorene)s.,   2006 03
  • Synthesis and Light-emitting Characteristics of Donor-Acceptor Type Perylenes.,   2006 03
  • Synthesis and Light-emitting Characteristics of Star-shaped Oligo(phenyleneethynylene)s.,   2006 03
  • Synthesis and Light-emitting Characteristics of p-Electron Systems Having Fluorene- and Bithiophene-units.,   2006 03
  • The Synthesis of p-Boronophenylalanine with the Trifluoromethyl Group and its Evaluation as Boron Carrier or MRI Probe,   2006 03
  • Donor-acceptor type perylene derivatives: Synthesis and Light-emitting Characteristics,   2005 12
  • Study on the compounds containing fuorine and boron-10 for the application to MRI and BNCT,   2005 12
  • Light-emitting Efficiency Tuning of Oligo(phenylene ethynylene)s (OPEs) by Donor and Acceptor Groups,   2005 12
  • Studies on the improvement of light-emitting efficiency in organic fluorophores,   2005 12
  • Synthesis of the dimer of azaarylenecyclyne,   2005 12
  • Synthesis and evaluation of the compounds containing 10B and 19F atoms as boron carrier and imaging agent,   2005 12
  • Novel Oligomeric p Conjugated Systems : Synthesis and Light- Emitting Charateristics,   2005 12
  • Study on the structure activity rerationship of a phytosiderophore, mugineic acid,   2005 12
  • Synthesis of glutathione conjugated bile acids,   2005 12
  • Synthesis and biological activity of fluorescent labeled analogs of the spider toxin NPTX-594,   2005 12
  • Study on the structure activity rerationship of a phytosiderophore, mugineic acid,   2005 11
  • Synthesis and evaluation of the compounds containing CF3 and B(OH)2 groups as boron carrier and MRI probe,   2005 11
  • Syntheses and 3D-structual analyses of α,β-dehydroalanine- and α,β-dehydrovaline-homopeptides,   2005 10
  • Synthesis and evaluation of the compounds containing 10B and 19F atoms as boron carrier and imaging agent,   2005 10
  • Synthesis and biological activity of fluorescent labeled analogs of the spider toxin NPTX-594,   2005 10
  • Study on the structure activity rerationship of a phytosiderophore, mugineic acid,   2005 10
  • Light-emitting Characteristics of Donor-Acceptor Type Oligo(arylene ethynylene)s,   2005 03
  • Light-emitting Characteristics of Linear π-Electron Systems Having Fluorene- and Bipyridine- units.,   2005 03
  • Synthesis and Light-emitting Properties of Novel Organic Luminophors Including Benzofuran Rings.,   2005 03
  • Study on synthesis and application of fluorine- and 10boron-containing amino acids to MRI and BNCT,   2004 12
  • Study on electron transfer of dehydroalanine oligopeptides,   2004 12
  • Structural study of novel acylpolyamine-toxins from the venom of Nephila clavipes, a Brazilian Joro spider,   2004 12
  • Study on the compounds containing fluorine and boron-10 for the application to MRI and BNCT,   2004 12
  • Study on the synthesis of fluorescent labeled analogs of spider toxin for clarification of glutamatergic neuromuscular transmission,   2004 12
  • Study on fluorine- and 10boron-containing compounds toward MRI and BNCT,   2004 11
  • Structural study of novel acylpolyaminetoxins from the venom of Nephila clavipes, a Brajilian spider,   2004 11
  • Study on fluorine- and/or boron-containing amino acids and their related compounds as tools for diagnosis and treatment of cancer,   2004 09
  • Creation of π-Electron Systems for Development of Organic Luminophores and Bioactive Compounds,   2004 07
  • Molecular Shape and Light-emitting Characteristics in Oligo(aryleneethynylene)s,   2004 06
  • Light-emitting Characteristics of Doughnut-shaped π-Electron Systems,   2004 04
  • Light-emitting Characteristics of Acyclic Compounds Having Benzene- and Pyridine-rings, and Triple Bonds.,   2004 03
  • Creation of Novel Organic Luminophors Including Benzofuran Ring Systems.,   2004 03
  • Synthetic study for the structure determination of novel peptides isolated from Brazilian Joro spider.,   2003 12
  • Synthetic study of the fluorescence-labeled spider toxin analogs for elucidating the mechanism of glutamate neurotransmission.,   2003 12
  • Study on a solid-phase synthesis of serine-containing peptides utilizing the characteristic of glutamic acid.,   2003 12
  • Study on electron transfer reaction of dehydropeptides .,   2003 12
  • Chemical Properties of Arene-azaarenecyclynes,   2003 12
  • Synthetic study of cyclic guanidinoamino acid tuberactidine.,   2003 12
  • Study on the solid-phase synthesis of serine-containing cyclic peptides utilizing the characteristics of glutamic acid.,   2003 12
  • Synthetic Study of Amino Acids Containing Fluorine and Boron for Diagnosis and Treatment of Cancer.,   2003 12
  • Study on the synthesis and structure of dehydropeptides.,   2003 12
  • Synthetic study of fluorescence-labeled mugineic acid analogs for elucidating the transfer mechanism of iron ion.,   2003 12
  • Creation of Organic Luminophores Having Benzene Rings, Triple Bonds and Heterocycles,   2003 12
  • Mysterious Reaction of Aromatic Hydrazones with TCNE Leading to Cyanocinnolines: Features, Key Intermediates, and Mechanism involving Heterolytic C-C Bond Cleavage, THE FOURTH INTERNATIONAL FORUM ON CHEMISTRY OF FUNCTIONAL ORGANIC CHEMICALS( IFOC-4),   2003 11 , THE FOURTH INTERNATIONAL FORUM ON CHEMISTRY OF FUNCTIONAL ORGANIC CHEMICALS( IFOC-4)
  • Synthetic study of the fluorescence-labeled spider toxin analogs for elucidating the mechanism of glutamate neurotransmission.,   2003 11
  • Light-emitting Characteristics of Doughnut-shape p-Electron Systems and Their Metal Complexes, The 4th International Forum on Chemistry of Functional Organic Chemicals,   2003 11 , The 4th International Forum on Chemistry of Functional Organic Chemicals
  • Study on the solid-phase synthesis of serine-containing cyclic peptides utilizing the characteristics of glutamic acid.,   2003 11
  • Study on the solid-phase synthesis of serine-containing cyclic peptides utilizing the characteristics of glutamic acid.,   2003 10
  • Synthesis and Structure of Thiaarenecyclynes and Their AgⅠ-complex,   2003 03
  • Creation of Organic Luminophors Having Benzene Rings, Triple Bonds and Heterocycles.,   2003 03
  • Light-emitting Properties of Arene.azaarenecyclynes.SbⅤcomplex,   2003 03
  • Reaction of 1.Methyl.cinnolinium Compound with Cyanoanion,   2003 03
  • Creation of heteroarenecyclynes and their C60 supramolecular complex,   2002 12
  • Study on a novel method for solid-phase synthesis utilizing the characteristic of glutamic acid,   2002 12
  • Study on the synthesis of NPTX?594 analogs for photoaffinity labeling with Ca2+ binding protein,   2002 12
  • Syntheric study of oligopeptides composed of β,β?disubstituted dehydro-alanine,   2002 12
  • Study on a novel method for solid-phase synthesis utilizing the characteristic of glutamic acid,   2002 12
  • Study on a solid-phase synthesis of serine?containing peptides utilizing the characteristic of glutamic acid,   2002 12
  • Study on solid-phase synthesis of cyclic-peptides containing asparagine and glutamine,   2002 12
  • Study on a solid-phase synthesis of cysteine?containing peptides utilizing the characteristic of glutamic acid,   2002 12
  • Synthesis and chemical properties of arene?azaarenecyclynes,   2002 12
  • Study of a practical method for preparation of introducing-reagents of the amino-protective groups utilizing triphosgene,   2002 12
  • Creation of Functional Saturn-Type C60 complex with Nanoheterocycles,   2002 10
  • Study on the solid-phase synthesis of cuclic peptides containing asparagine or glutamine,   2002 10
  • Study on solid-phase synthesis of compounds, containing hydroxyamino acids or saccharides, by taking advantage of the characteristics of glutamic acid,   2002 09
  • Study on solid?phase synthesis of compounds, containing hydroxyamino acids or saccharides, by taking advantage of the characteristics of glutamic acid,   2002 09
  • Nano-sized Heteroarenecyclynes: Synthesis and Tunability as Receptors for Fullerene C60,   2002 07
  • Multi-Functionalization of Fullerene C60 with Heterocyclic Five-Membered Ring: Synthesis and Emission Characteristics,   2002 07
  • Creation of nanoscale heteroarene cyclynes and their functional supramolecular complexes with C60,   2002 06
  • Shape-persisted azamacrocycles: synthesis and light-emitting characteristics,   2002 06
  • Synthetic Reaction Using Tetrabromomethane as σ Electron Acceptor: Reaction of Dimetylaniline with CBr4 producing 4, 4, Metylenebis (N, N dimetylaniline),   2002 03
  • Reaction of Aromatic Hydrazones with TCNE in Acetonitrile Leading to the formation of Cyanocinnoline,   2002 03
  • Synthetic studies on Broussonetine J,   2002 03
  • Synthetic study of joro spider toxin NPTX 594 analogs to elucidate the glutamate receptor,   2002 03
  • Synthesis and light-emitting properties of arene azaarene cyclynes,   2002 03
  • Design and Synthesis of Fluoro Substituted 1, 3 Diphenyl 2 pyrazoline Derivatives toward to Photostable and Storongly Fluoresent Organic Materials,   2002 03
  • Synthesis, structure and chemical properties of thiaarene cyclynes,   2002 03
  • Synthesis of Nano Crown Ethers,   2002 03
  • Synthesis of Novel Cyclynes Containing Imidazole Rings and Benzene Rings,   2002 03
  • Creation and function of heteroarene cyclynes C60 supramolecular complexes,   2002 03
  • Study on solid phase synthesis of compounds, containing hydroxyamino acids or saccharides, by taking advantage of the characteristics of glutamic acid,   2001 12
  • Novel Nanomacrocycles Synthesis and Characteristic Properties of Arenecyclynes,   2001 12
  • Study on peptides inhibiting the activation of gelatinase A (MMP 2),   2001 12
  • Synthetic Studies on Bioactive Natural Products Containing Pyrrolidine Ring,   2001 12
  • Creation of Nanoscale Oxaarenecyclynes and Their Saturn-type Supramolecular Complexes with C60,   2001 11
  • Creation of Novel Nanoscale Arene azaarene Cyclynes,   2001 11
  • Study on peptides inhibiting the activation of gelatinase A (MMP 2),   2001 10
  • Constraction of Nanostructure from Nanohetrocycles or Five Membered Heterocycles and C60, and Development of Their Novel Functions,   2001 10
  • Creation of The Novel Nanomacrocycles, Arenecyclynes,   2001 10
  • Study on solid-phase synthesis of compounds, containing hydroxyamino acids or saccharides, by taking advantage of the characteristics of glutamic acid,   2001 10
  • Creation of Supramolecular Complexes with Supermacrocyclic Crown Ethers as the Receptor,   2001 03
  • Synthesis of Supermacrocycles Having Diethynylbenzene Units and Thioether Linkages, and Creation of Their Supramolecular Complex,   2001 03
  • Synthesis of Supermacrocyclic Oxacyclynes Containing Benzene Rings and Ether Linkages, and Creation of Their C60 Supramolecular Complex,   2001 03
  • Synthesis and Characteristic Poperties of Novel Cyclynes Containing Pyridine Rings and benzene Rings,   2001 03
  • Emissivity of fluorescence of ring-fused C60 derivatives,   2001 03
  • Synthesis and Characteristic Properties of Novel Hybrid Thiacyclynes,   2001 03
  • Electrochemical Transformation of 4 Cyanocinnolines into 4(1H) Cinnolones,   2001 03
  • Synthetic Reaction Using Tetrabromomethane as σ Electron Acceptor: Reaction of Dimetylaniline with CBr4 producing 4,4' Metylenebis(N, N dimetylaniline),   2001 03

Misc

  • Creation of strongly light-emitting p-conjugated molecules, 15, 18,   2007 10
  • Donor/Acceptor Modification of Rod-shaped p Conjugated Carbon Framework: Synthesis, Light-emitting Characteristics, and Entropy Dependence of Emission Efficiency., 33, 36,   2007 01
  • New Fluorophores with Rod-shaped Polycyano p conjugated Structures: Synthesis and Light-emitting Characteristics., JSPS 116 Committee Report, 59, 2, 32, 35,   2006 06
  • Creation of Novel Organic Fluorophores Containing Benzofuran Rings,   2006 04
  • Star-Shaped p Electron Systems That Comprise 1,3,5-Tri-Substitued Benzene Core and Oligo(aryleneethynylene) Arms: Synthesis, Light-Emitting Characteristics, and pi Conjugation between The Arms., JSPS 116 Committee Report, 58, 32, 35,   2006 01
  • Light-emitting Efficiency Control by Donor and Acceptor Groups, 40, 43,   2005 06
  • Creation, Physical Properties, and Functions of Novel Nanocyclynes, Nanorods, and Nanotubes.,   2004 04
  • Oligo(m-Aryleneethynylene)s: Synthesis and Light-emitting Characteristics, 56, 25, 28,   2004 01
  • Creation of Bicapped and Saturn-Type C60 Complexes, and The Development of Their Novel Function., 44, 67,   2003 03
  • Creation, Properties, and Chemical Behavior of Saturn-Type C60 Complexes., 1, 88, 89,   2003 03
  • Creation and Characteristic Properties of Hybrid Cyclynes in which Phenylene and Heteroatom Groups are Alternately Inserted into The Single Bonds of Cyclooctatetrayne, 55, 175, 178,   2003 01
  • Chemical Transformation of Nonfluorescent C60 into the Strongly Fluorescent Derivatives, 54, 6, 9,   2002 06
  • Study on solid phase synthesis of compounds, containing hydroxyamino acids or saccharides, by taking advantage of the characteristics of glutamic acid, 391, 394,   2002 03
  • Creation of five membered heterocyclic ring-fused C60 derivatives, 69, 72,   2001 03
  • Creation, Properties, and Chemical Behavior of Saturn-Type C60 Complexes,   2001 03