Publication List(1994)

One-pot Synthesis of Homoallylic Alcohols from 1,3-Dienes: Tandem Vicinal Difunctionalization of 1,3-Dienes by Hydride Addition-Aldehyde Coupling Sequence via Organosilicon Intermediates,
S. Kobayashi, K. Nishio,
Synthesis, 1994, 457-459.

A Catalytic Asymmetric Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Ketones Using a Chiral Titanium Oxide,
S. Kobayashi, S. Suda, M. Yamada, T. Mukaiyama,
Chem. Lett., 1994, 97-100.

A Novel Chiral Catalyst System, Tin(II) Triflate, a Chiral Diamine, and Tin(II) Oxide, in Asymmetric Aldol Reactions,
S. Kobayashi, T. Kawasuji, N. Mori,
Chem. Lett., 1994, 217-220.

Enantioselective Synthesis of Both Diastereomers Including α-Alkoxy-β-hydroxy-β-methyl Units,
S. Kobayashi, M. Horibe,
Synlett, 1994, 147-148.

Lanthanide(III)-catalyzed Enantioselective Diels-Alder Reactions. Stereoselective Synthesis of Both Enantiomers by Using a Single Chiral Source and a Choice of Achiral Ligands,
S. Kobayashi, H. Ishitani,
J. Am. Chem. Soc., 116, 4083-4084 (1994).

Scandium(III) Perchlorate (Sc(ClO4)3). A Novel Catalyst in the α-C- and N-Glycosylation Reactions,
I. Hachiya, S. Kobayashi,
Tetrahedron Lett., 35, 3319-3320 (1994).

Anti-Selective Asymmetric Aldol Reactions. Enantioselective Synthesis of anti-α,β-Dihydroxy Phenyl Ester Derivatives,
S. Kobayashi, T. Kawasuji,
Tetrahedron Lett., 35, 3329-3332 (1994).

Diastereo- and Enantioselective Synthesis of syn-and anti-1,2-Diol Units by Asymmetric Aldol Reactions,
T. Mukaiyama, I. Shiina, H. Uchiro, S. Kobayashi,
Bull. Chem. Soc. Jpn., 67, 1708-1716 (1994).

Lanthanide Triflates as Water-tolerant Lewis Acids. Activation of Commercial Formaldehyde Solution and Use in the Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous Media,
S. Kobayashi, I. Hachiya,
J. Org. Chem., 59, 3590-3596 (1994).

Repeated Use of the Catalyst in Ln(OTf)3-catalyzed Aldol and Allylation Reactions,
S. Kobayashi, I. Hachiya, Y. Yamanoi,
Bull. Chem. Soc. Jpn., 67, 2342-2344 (1994).

Scandium Trifluoromethanesulfonate. A Novel Catalyst for Friedel-Crafts Acylation,
A. Kawada, S. Mitamura, S. Kobayashi,
Synlett, 1994, 545-546.

A Chiral Scandium Catalyst for Enantioselective Diels-Alder Reactions,
S. Kobayashi, M. Araki, I. Hachiya,
J. Org. Chem., 59, 3758-3759 (1994).

Enantioselective Synthesis of Both Diastereomers, Including the α-Alkoxy-β-hydroxy-β-methyl(phenyl) Units, by Chiral Tin(II) Lewis Acid-mediated Asymmetric Aldol Reactions,
S. Kobayashi, M. Horibe, Y. Saito,
Tetrahedron, 50, 9629-9642 (1994).

Characterization of Chiral Ytterbium and Scandium Catalysts Based on Their Trifluoromethanesulfonates in Asymmetric Diels-Alder Reactions,
S. Kobayashi, H. Ishitani, M. Araki, I. Hachiya,
Tetrahedron Lett., 35, 6325-6328 (1994).

Rare Earth Metal Trifluoromethanesulfonates as Water-tolerant Lewis Acid Catalysts in Organic Synthesis,
S. Kobayashi,
Synlett, 1994, 689-701.

Chiral Lewis Acids as Efficient Catalysts in Asymmetric Synthesis,
T. Mukaiyama, S. Kobayashi,
Stereocontrolled Organic Synthesis, ed by B. M. Trost, pp. 37-65, Blackwell Scientific Publications (1994).

Facile Synthesis of Both syn and anti Homoallylic Alcohols from Allyl Chlorides via Organosilicon Intermediates,
S. Kobayashi, K. Nishio,
Chem. Lett., 1994, 1773-1776.

Asymmetric Diels-Alder Reactions Catalyzed by Chiral Lanthanide(III) Trifluoromethanesulfonates. Unique Structure of the Triflate and Stereoselective Synthesis of Both Enantiomers Using a Single Chiral Source and a Choice of Achiral Ligands,
S. Kobayashi, H. Ishitani, I. Hachiya, M. Araki,
Tetrahedron, 50, 11623-11636 (1994).

Highly Enantioselective Synthesis of Enantiomeric 2,3-Dihydroxythioesters by Using Similar Types of Chiral Sources Derived from L-Proline,
S. Kobayashi, M. Horibe,
J. Am. Chem. Soc., 116, 9805-9806 (1994).

Facile and Highly Stereoselective Synthesis of Homoallylic Alcohols Using Organosilicon Intermediates,
S. Kobayashi, K. Nishio,
J. Org. Chem., 59, 6620-6628 (1994).

Enantioselective Syntheses of D-erythro-Sphingosine and Phytosphingosine from Simple Achiral Aldehydes Using Catalytic Asymmetric Aldol Reactions as Key Steps,
S. Kobayashi, T. Hayashi, T. Kawasuji,
Tetrahedron Lett., 35, 9573-9576 (1994).