Publication List(1990-1991)
Catalytic Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes by the Use of Chiral Diamine Coordinated Tin(II) Triflate,
T. Mukaiyama, S. Kobayashi, H. Uchiro, I. Shiina,
Chem. Lett., 1990, 129-132.
New Role of Tin(II) Compounds in Organic Synthesis,
T. Mukaiyama, S. Kobayashi,
J. Organomet. Chem., 382, 39-52 (1990).
[1,1'-Bi-2-naphthalenediolato(2-)-O,O']oxotitanium. An Efficient Chiral Catalyst for the Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes,
T. Mukaiyama, A. Inubushi, S. Suda, R. Hara, S. Kobayashi,
Chem. Lett., 1990, 1015-1018.
Facile Synthesis of Optically Active anti-α,β-Dihydroxy Ester Derivatives,
T. Mukaiyama, H. Uchiro, I. Shiina, S. Kobayashi,
Chem. Lett., 1990, 1019-1022.
A New Efficient Chiral Catalyst System. Combined Use of Tin(II) Oxide, Trimethylsilyl Triflate and Chiral Diamine in the Asymmetric Aldol Reaction,
T. Mukaiyama, H. Uchiro, S. Kobayashi,
Chem. Lett., 1990, 1147-1150.
Asymmetric Aldol-type Reaction between Both Achiral Ketene Silyl Acetals of Acetic Acid Esters and Aldehydes by the Use of a Chiral Promoter,
T. Mukaiyama, S. Kobayashi, T. Sano,
Tetrahedron, 46, 4653-4662 (1990).
The Efficient Catalytic Asymmetric Aldol-type Reaction,
S. Kobayashi, Y. Fujishita, T. Mukaiyama,
Chem. Lett., 1990, 1455-1458.
Regioselective Condensation of Ethynyl Vinyl Ketone or 2-Propynyl Ether Derivatives with Silyl Enol Ethers Catalyzed by Trityl Perchlorate,
T. Mukaiyama, S. Matsui, K. Homma, S. Kobayashi,
Bull. Chem. Soc. Jpn., 63, 2687-2690 (1990).
A Convenient and Versatile Route for the Stereoselective Synthesis of Monosaccharides via Key Chiral Synthons Prepared from Achiral Sources,
T. Mukaiyama, I. Shiina, S. Kobayashi,
Chem. Lett., 1990, 2201-2204.
An Effective Activation of O-Trimethylsilyl Monothioacetal under Extremely Mild Conditions Using a Novel Catalyst System, Trimethylsilyl Chloride and Indium(III) Chloride,
T. Mukaiyama, T. Ohno, T. Nishimura, J. S. Han, S. Kobayashi,
Chem. Lett., 1990, 2239-2242.
A Facile Synthesis of Cyanohydrin Trimethylsilyl Ethers by the Addition Reaction of Trimethylsilyl Cyanide with Aldehydes under Basic Condition,
S. Kobayashi, Y. Tsuchiya, T. Mukaiyama,
Chem. Lett., 1991, 537-540.
Enantioselective Addition Reaction of Trimethylsilyl Cyanide with Aldehydes Using a Chiral Tin(II) Lewis Acid,
S. Kobayashi, Y. Tsuchiya, T. Mukaiyama,
Chem. Lett., 1991, 541-544.
The Chiral Catalyst Control. A Significant Role of a Chiral Catalyst in the Diastereoselective Aldol Reaction Using Chiral Aldehydes,
S. Kobayashi, A. Ohtsubo, T. Mukaiyama,
Chem. Lett., 1991, 831-834.
Asymmetric Aldol Reaction between Achiral Silyl Enol Ethets and Achiral Aldehydes by Use of a Chiral Promoter System,
S. Kobayashi, H. Uchiro, Y. Fujishita, I. Shiina, T. Mukaiyama,
J. Am. Chem. Soc., 113, 4247-4252 (1991).
Reversal Phenomena of the Preferential Activation of Aldehydes to the Corresponding Acetals under Non-Basic Conditions. The Chemoselective Aldol Reaction of Aldehydes with t-Butyldimethylsilyl Enol Ethers Using TBSCl-InCl3 as a Catalyst,
T. Mukaiyama, T. Ohno, J. S. Han, S. Kobayashi,
Chem. Lett., 1991, 949-952.
Highly Enantioselective Synthesis of Propargylic Alcohols by Way of the Asymmetric Aldol Reaction,
T. Mukaiyama, M. Furuya, A. Ohtsubo, S. Kobayashi,
Chem. Lett., 1991, 989-992.
The Catalytic Friedel-Crafts Acylation Reaction Using a Catalyst Generated from GaCl3 and a Silver Salt,
T. Mukaiyama, T. Ohno, T. Nishimura, S. Suda, S. Kobayashi,
Chem. Lett., 1991, 1059-1062.
An Efficient Asymmetric Aldol Reaction Promoted by a Chiral Tin(II) Lewis Acid Consisting of Tin(II) Triflate, (R)-2-[(N-1-Naphthylamino)methyl]tetrahydrothiophene and a Tin(IV) Compound,
T. Mukaiyama, H. Asanuma, I. Hachiya, S. Kobayashi,
Chem. Lett., 1991, 1209-1212.
The Asymmetric Diels-Alder Reaction of α,β-Unsaturated Aldehydes with Dienes Using a Chiral Boron Reagent as a Catalyst,
S. Kobayashi, M. Murakami, T. Harada, T. Mukaiyama,
Chem. Lett., 1991, 1341-1344.
A Novel Catalyst System, Trimethylsilyl Chloride and Indium(III) Chloride, as an Efficient Catalyst in the Sulfide Synthesis,
T. Mukaiyama, T. Ohno, T. Nishimura, J. S. Han, S. Kobayashi,
Bull. Chem. Soc. Jpn., 64, 2524-2527 (1991).
Comparison of the Asymmetric Environments Created by the Chiral Tin(II) Lewis Acids in the Enantioselective Aldol Reaction of Silyl Enol Ethers with Aldehydes,
S. Kobayashi, T. Harada, J. S. Han,
Chem. Express, 6, 563-566 (1991).
Catalytic Asymmetric Aldol Reaction of the Silyl Enol Ether of Acetic Acid Thioester with Aldehydes Using Chiral Tin(II) Lewis acid,
S. Kobayashi, M. Furuya, A. Ohtsubo, T. Mukaiyama,
Tetrahedron:Asymmetry, 2, 635-638 (1991).
Highly Enantioselective Synthesis of syn-α,β-Dihydroxy Thioesters by the Asymmetric Aldol Reaction Using a Chiral Tin(II) Lewis Acid,
T. Mukaiyama, I. Shiina, S. Kobayashi,
Chem. Lett., 1991, 1901-1904.
Lanthanide Trifluoromethanesulfonates as Stable Lewis Acids in Aqueous Media. Yb(OTf)3 Catalyzed Hydroxymethylation Reaction of Silyl Enol Ethers with Commercial Formaldehyde Solution,
S. Kobayashi,
Chem. Lett., 1991, 2187-2190.
The Catalytic Friedel-Crafts Acylation Reaction and the Catalytic Beckmann Rearrangement Promoted by a Gallium(III) or an Antimony(V) Cationic Species,
T. Harada, T. Ohno, S. Kobayashi, T. Mukaiyama,
Synthesis, 1991, 1216-1220.