Publication List(1997)
The Catalytic
Fries Rearrangement and O-Acylation Reactions Using Group 3 and 4 Metal Triflates as Catalysts,
S. Kobayashi, M. Moriwaki, I. Hachiya,
Bull. Chem. Soc. Jpn., 70, 267-273 (1997).
Facile Synthesis of α-Amino Nitriles Using Lanthanide Triflate as a Lewis Acid Catalyst,
S. Kobayashi, H. Ishitani, M. Ueno,
Synlett, 1997, 115-116.
Aldehydes vs. Aldimines. Unprecedented Reactivity in their Enolate Addition Reactions,
S. Kobayashi, S. Nagayama,
J. Org. Chem., 62, 232-233 (1997).
The Asymmetric Synthesis of Sphingofungin F and the Determination of Its Stereochemistry,
S. Kobayashi, M. Matsumura, T. Furuta, T. Hayashi, S. Iwamoto,
Synlett, 1997, 301-303.
Chiral Lewis Acid-controlled Synthesis (CLAC Synthesis). Chiral Lewis Acids Influence the Reaction Course in Asymmetric Aldol Reactions for the Synthesis of Enantiomeric Dihydroxythioester Derivatives in the Presence of Chiral Diamines Derived from L-Proline,
S. Kobayashi, M. Horibe,
Chem., Eur. J., 3, 1472-1481 (1997).
Facile Synthesis of 3,4-Dihydro-&plpha;-pyrones via Michael Reaction-O-Acylation Sequences,
S. Kobayashi, M. Moriwaki,
Synlett, 1997, 551-552.
Catalytic Enantioselective Mannich-type Reactions Using a Novel Chiral Zirconium Catalyst,
H. Ishitani, M. Ueno, S. Kobayashi,
J. Am. Chem. Soc., 119, 7153-7154 (1997).
The Polymer Effect on Catalysts. Aldimine-selective Reactions in the Coexistence of Aldehydes Using a Polymer-supported Scandium Catalyst,
S. Kobayashi, S. Nagayama,
Synlett, 1997, 653-654.
Lewis Acid Catalysis in Micellar Systems. Sc(OTf)3-catalyzed Aqueous Aldol Reactions of Silyl Enol Ethers with Aldehydes in the Presence of a Surfactant,
S. Kobayashi, T. Wakabayashi, S. Nagayama, H. Oyamada,
Tetrahedron Lett., 38, 4559-4562 (1997).
5-(4'-Chloromethylphenyl)pentylpolystyrene Resin (CMPP resin). A New Linker Resin for Solid-Phase Organic Synthesis Under Lewis Acidic Conditions,
S. Kobayashi, M. Moriwaki,
Tetrahedron Lett., 38, 4251-4254 (1997).
Three-component or Four-component Coupling Reactions Leading to δ-Lactams. Facile Synthesis of γ-Acyl-δ-Lactams from Silyl Enolates, α,β-Unsaturated Thioesters, and Imines or Amines and Aldehydes via Tandem Michael-Imino Aldol Reactions,
S. Kobayashi, R. Akiyama, M. Moriwaki,
Tetrahedron Lett., 38, 4819-4822 (1997).
Use of an Organometallic Reagent in Water : Sc(OTf)3-catalyzed Allylation Reactions of Aldehydes in Micellar Systems,
S. Kobayashi, T. Wakabayashi, H. Oyamada,
Chem. Lett., 1997, 831-832.
Group 4 Metal Triflates as Efficient Catalysts for Allylations of Imines with Allyltributylstannane and Mannich-type Reaction of Imines with Silyl Enol Ethers,
S. Kobayashi, S. Iwamoto, S. Nagayama,
Synlett, 1997, 1099-1101.
Lewis Acid Catalysis in Aqueous Media: Copper(II)-catalyzed Aldol and Allylation Reaction in a Water-Ethanol-Toluene Solution,
S. Kobayashi, S. Nagayama, T. Busujima,
Chem. Lett., 1997, 959-960.
Lanthanide Triflate-catalyzed Three-component Coupling Reactions of Aldehydes, Hydroxylamines, and Alkenes Leading to Isoxazolidine Derivatives,
S. Kobayashi, R. Akiyama, M. Kawamura, H. Ishitani,
Chem. Lett.,1997, 1039-1040.
Aldehydes vs. Aldimines. Unprecedented Aldimine-Selective Nucleophilic Additions in the Coexistence of Aldehydes Using a Lanthanide Salt as a Lewis Acid Catalyst,
S. Kobayashi, S. Nagayama,
J. Am. Chem. Soc., 119, 10049-10053 (1997).
Evaluation of a Trans Configuration for the Apoptosis-inducing Activity of Ceramide,
E. Kishida, M. Kasahara, Y. Takagi,M. Matsumura, T. Hayashi, S. Kobayashi, Y. Masuzawa,
J. Lipid Mediat. Cell, 16, 127-137 (1997).