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,
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,
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,
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,
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,
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).