Yoshinori Nishii

Summary

Affiliation: Shinshu University
Country: Japan

Publications

  1. ncbi request reprint Photochemical behavior of some p-styrylstilbenes and related compounds: spectral properties and photoisomerization in solution and in solid state
    Zhu Fengqiang
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Photochem Photobiol 82:1645-50. 2006
  2. ncbi request reprint Regiocontrolled benzannulation of diaryl(gem-dichlorocyclopropyl)methanols for the synthesis of unsymmetrically substituted alpha-arylnaphthalenes: application to total synthesis of natural lignan lactones
    Yoshinori Nishii
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    J Org Chem 70:2667-78. 2005
  3. doi request reprint Chemiluminescence of 4-styrylphthal-hydrazides with crown ether as ionophore
    Jiro Motoyoshiya
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Luminescence 23:37-41. 2008
  4. ncbi request reprint Fluorescence quenching of versatile fluorescent probes based on strongly electron-donating distyrylbenzenes responsive to aromatic chlorinated and nitro compounds, boronic acid and Ca(2+)
    Jiro Motoyoshiya
    Department of Chemistry, Shinshu University, Ueda, Nagano 386 8567, Japan
    Spectrochim Acta A Mol Biomol Spectrosc 69:167-73. 2008
  5. ncbi request reprint Highly stereoselective radical carbonylations of gem-dihalocyclopropane derivatives with CO
    Yoshinori Nishii
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Org Lett 9:563-6. 2007
  6. ncbi request reprint Chirality exchange from sp3 central chirality to axial chirality: benzannulation of optically active diaryl-2,2-dichlorocyclopropylmethanols to axially chiral alpha-arylnaphthalenes
    Yoshinori Nishii
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    J Am Chem Soc 126:5358-9. 2004
  7. doi request reprint Practical, general, and systematic method for optical resolution of gem-dihalo- and monohalocyclopropanecarboxylic acids utilizing chiral 1,1'-binaphtholmonomethyl ethers: application to the synthesis of three chiral pesticides
    Hiroaki Yasukochi
    Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2 1 Gakuen, Sanda, Hyogo 669 1337, Japan
    Org Biomol Chem 6:540-7. 2008
  8. doi request reprint Toward a chemiluminescent molecular device: metal ion-enhanced chemiluminescence of benzylidenacridan with 15-monoazacrown-5
    Jiro Motoyoshiya
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano, 386 8567, Japan
    J Org Chem 74:1014-8. 2009
  9. ncbi request reprint Unprecedented chemiluminescence behaviour during peroxyoxalate chemiluminescence of oxalates with fluorescent or electron-donating aryloxy groups
    Ryu Koike
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Luminescence 21:164-73. 2006

Collaborators

Detail Information

Publications9

  1. ncbi request reprint Photochemical behavior of some p-styrylstilbenes and related compounds: spectral properties and photoisomerization in solution and in solid state
    Zhu Fengqiang
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Photochem Photobiol 82:1645-50. 2006
    ..Additionally, the (Z,E,Z)-4,4'-styrylstilbene was found to undergo a one-way photoisomerization to the E,E,E-isomer via the E,E,Z-isomer in solution and the crystalline E,E,Z-isomer to the E,E,E-isomer in the solid state...
  2. ncbi request reprint Regiocontrolled benzannulation of diaryl(gem-dichlorocyclopropyl)methanols for the synthesis of unsymmetrically substituted alpha-arylnaphthalenes: application to total synthesis of natural lignan lactones
    Yoshinori Nishii
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    J Org Chem 70:2667-78. 2005
    ....
  3. doi request reprint Chemiluminescence of 4-styrylphthal-hydrazides with crown ether as ionophore
    Jiro Motoyoshiya
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Luminescence 23:37-41. 2008
    ....
  4. ncbi request reprint Fluorescence quenching of versatile fluorescent probes based on strongly electron-donating distyrylbenzenes responsive to aromatic chlorinated and nitro compounds, boronic acid and Ca(2+)
    Jiro Motoyoshiya
    Department of Chemistry, Shinshu University, Ueda, Nagano 386 8567, Japan
    Spectrochim Acta A Mol Biomol Spectrosc 69:167-73. 2008
    ..These results suggest a potential use of these types of compounds as sensors for strongly electron-withdrawing substances and a suitable metal cation...
  5. ncbi request reprint Highly stereoselective radical carbonylations of gem-dihalocyclopropane derivatives with CO
    Yoshinori Nishii
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Org Lett 9:563-6. 2007
    ..Inherently less reactive gem-dichloro- and bromochlorocyclopropanes than gem-dibromocyclopropanes served as favorable substrates. [reaction: see text]...
  6. ncbi request reprint Chirality exchange from sp3 central chirality to axial chirality: benzannulation of optically active diaryl-2,2-dichlorocyclopropylmethanols to axially chiral alpha-arylnaphthalenes
    Yoshinori Nishii
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    J Am Chem Soc 126:5358-9. 2004
    ..This unique transformation involves the single-step chirality exchange from sp3 central chirality to axial chirality, that is, a type of excellent memory effect...
  7. doi request reprint Practical, general, and systematic method for optical resolution of gem-dihalo- and monohalocyclopropanecarboxylic acids utilizing chiral 1,1'-binaphtholmonomethyl ethers: application to the synthesis of three chiral pesticides
    Hiroaki Yasukochi
    Department of Chemistry, School of Science and Technology, Kwansei Gakuin University, 2 1 Gakuen, Sanda, Hyogo 669 1337, Japan
    Org Biomol Chem 6:540-7. 2008
    ..Pyrethroid with three asymmetric centers was efficiently synthesized in a much better yield compared with the reported method...
  8. doi request reprint Toward a chemiluminescent molecular device: metal ion-enhanced chemiluminescence of benzylidenacridan with 15-monoazacrown-5
    Jiro Motoyoshiya
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano, 386 8567, Japan
    J Org Chem 74:1014-8. 2009
    ..Thus, the possibility of metal ion sensing by a chemiluminescent molecular device is suggested...
  9. ncbi request reprint Unprecedented chemiluminescence behaviour during peroxyoxalate chemiluminescence of oxalates with fluorescent or electron-donating aryloxy groups
    Ryu Koike
    Department of Chemistry, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano 386 8567, Japan
    Luminescence 21:164-73. 2006
    ..These experimental results suggest that such emitting species would be formed by an intra- and intermolecular electronic interaction with a high-energy intermediate, such as a dioxetanone...