Publication List(1992-1993)

Stereoselective Synthesis of Both Diastereomers of the α-Methyl-β-hydroxy-β-alkyl(aryl) Units by Use of Tin(II) Triflate-mediated Aldol Reaction,
S. Kobayashi, I. Hachiya,
J. Org. Chem., 57, 1324-1326 (1992).


An Efficient Method for the Preparation of Chiral Synthons Starting from Racemic Compounds by Way of Asymmetric Synthesis,
S. Kobayashi, I. Shiina, J. Izumi, T. Mukaiyama,
Chem. Lett., 1992, 373-376.


A Novel Catalyst System, Antimony(V) Chloride-Lithium Perchlorate (SbCl5-LiClO4), in the Friedel-Crafts Acylation Reaction,
T. Mukaiyama, K. Suzuki, J. S. Han, S. Kobayashi,
Chem. Lett., 1992, 435-438.


The Aldol Reaction of Silyl Enol Ethers with Aldehyedes in Aqueous Media,
S. Kobayashi, I. Hachiya,
Tetrahedron Lett., 33, 1625-1628 (1992).


Stereoselective Synthesis of 1,2-cis-Arabinofuranosides Using a New Titanium Catalyst,
T. Mukaiyama, M. Yamada, S. Suda, Y. Yokomizo, S. Kobayashi,
Chem. Lett., 1992, 1401-1404.


Lanthanide Trifluoromethanesulfonates as Reusable Catalysts. Michael and Diels-Alder Reactions,
S. Kobayashi, I. Hachiya, T. Takahori, M. Araki, H. Ishitani,
Tetrahedron Lett., 33, 6815-6818 (1992).


An Efficient Synthesis of 6-Deoxy-D-allose from Simple Achiral Starting Materials,
S. Kobayashi, S. Onozawa, T. Mukaiyama,
Chem. Lett., 1992, 2419-2422.


Catalytic Asymmetric Aldol-type Reaction Using a Chiral Tin(II) Lewis Acid,
S. Kobayashi, H. Uchiro, I. Shiina, T. Mukaiyama,
Tetrahedron, 49, 1761-1772 (1993).


Novel Reactive Silyl Enolates. Highly Stereoselective Aldol and Michael Reactions without Catalysts,
S. Kobayashi, K. Nishio,
J. Org. Chem., 58, 2647-2649 (1993).


Facile and Highly Stereoselective Allylation of Aldehydes Using Allyltrichlorosilanes in DMF,
S. Kobayashi, K. Nishio,
Tetrahedron Lett., 34, 3453-3456 (1993).


Scandium Trifluoromethanesulfonate (Sc(OTf)3). A Novel Reusable Catalyst in the Diels-Alder Reaction,
S. Kobayashi, I. Hachiya, M. Araki, H. Ishitani,
Tetrahedron Lett., 34, 3755-3758 (1993).


Lanthanide Trifluoromethanesulfonates as Reusable Catalysts: Catalytic Friedel-Crafts Acylation,
A. Kawada, S. Mitamura, S. Kobayashi,
J. Chem. Soc., Chem. Commun., 1993, 1157-1158.


Asymmetric Diels-Alder Reaction Catalyzed by a Chiral Ytterbium Trifluoromethanesulfonate,
S. Kobayashi, I. Hachiya, H. Ishitani, M. Araki,
Tetrahedron Lett., 34, 4535-4538 (1993).


Scandium Trifluoromethanesulfonate (Sc(OTf)3) as a Novel Reusable Lewis Acid Catalyst in Aldol and Michael Reactions,
S. Kobayashi, I. Hachiya, H. Ishitani, M. Araki,
Synlett, 1993, 472-474.


Facile Syntheses of Amino-6-deoxyaldohexoses from Simple Achiral Starting Materials,
T. Mukaiyama, H. Anan, I. Shiina, S. Kobayashi,
Bull. Soc. Chim. Fra., 130, 388-394 (1993).


Enantioselective Synthesis of the α-Hydroxy-α-Methyl-β-Hydroxy Units via Asymmetric Aldol Reaction,
T. Mukaiyama, I. Shiina, J. Izumi, S. Kobayashi,
Heterocycles, 35, 719-724 (1993).


Aluminum Triflate-mediated Aldol Reactions. Stereoselective Synthesis of Both Diastereomers Including the α-Alkoxy-β-hydroxy-β-methyl Units,
S. Kobayashi, M. Horibe,
Synlett, 1993, 855-857.


Aqueous Reactions with a Lewis Acid and an Organometallic Reagent. The Scandium Trifluoromethanesulfonate (Sc(OTf)3)-Catalyzed Allylation Reaction of Carbonyl Compounds with Tetraallyltin,
I. Hachiya, S. Kobayashi,
J. Org. Chem., 58, 6958-6960 (1993).


A New Synthetic Route to Monosaccharides from Simple Achiral Compounds by Using a Catalytic Asymmetric Aldol Reaction as a Key Step,
S. Kobayashi, T. Kawasuji,
Synlett, 1993, 911-913.