Publication List(1984-1989)

A Facile Synthesis of α-Glucosides and α-Ribosides from the Corresponding 1-O-Acyl Sugars and Alcohols in the Presence of Trityl Perchlorate,
T. Mukaiyama, S. Kobayashi, S. Shoda,
Chem. Lett., 1984, 907-910.


A Facile Synthesis of α-C-Ribofuranosides from 1-O-Acetyl Ribose in the Presence of Trityl Perchlorate,
T. Mukaiyama, S. Kobayashi, S. Shoda,
Chem. Lett., 1984, 1529-1530.


Trityl Perchlorate as an Efficient Catalyst in the Aldol-type Reaction,
T. Mukaiyama, S. Kobayashi, M. Murakami,
Chem. Lett., 1984, 1759-1762.


An Efficient Method for the Preparation of threo Cross-Aldols from Silyl Enol Ethers and Aldehydes Using Trityl Perchlorate as a Catalyst,
T. Mukaiyama, S. Kobayashi, M. Murakami,
Chem. Lett., 1985, 447-450.


The Trityl Perchlorate Catalyzed Michael Reaction,
S. Kobayashi, M. Murakami, T. Mukaiyama,
Chem. Lett., 1985, 953-956.


Trityl Salts as Efficient Catalysts in the Aldol Reaction,
S. Kobayashi, M. Murakami, T. Mukaiyama,
Chem. Lett., 1985, 1535-1538.


Trityl Perchlorate Catalyzed Tandem Michael-aldol Reaction. A Facile Method for the Stereoselective Syntheses of γ-Acyl Substituted δ-Hydroxy Ketone Derivatives,
S. Kobayashi, T. Mukaiyama,
Chem. Lett., 1986, 221-224.


The Stereoselective Michael Reaction between Silyl Enol Ethers and α,β-Unsaturated Ketones by the Use of Trityl Perchlorate as a Catalyst,
T. Mukaiyama, M. Tamura, S. Kobayashi,
Chem. Lett., 1986, 1017-1020.


A Highly Stereoselective Synthesis of γ-Acyl-δ-lactones by the Trityl Perchlorate Catalyzed Tandem Michael-aldol Reaction,
S. Kobayashi, T. Mukaiyama,
Chem. Lett., 1986, 1805-1808.


The Highly Stereoselective Michael Reaction of α,β-Unsaturated Ketones with Silyl Enol Ethers of Thioesters Catalyzed by Trityl Salts. A Facile Stereoselective Synthesis of 5-Oxocarboxylic Acid Ester Derivatives,
T. Mukaiyama, M. Tamura, S. Kobayashi,
Chem. Lett., 1986, 1817-1820.


The Double Michael Reaction of α,β-Unsaturated Ketones with Siloxydienes Catalyzed by Trityl Perchlorate,
T. Mukaiyama, Y. Sagawa, S. Kobayashi,
Chem. Lett., 1986, 1821-1824.


The Tandem Michael-aldol Reaction Catalyzed by Trityl Perchlorate,
T. Mukaiyama, S. Kobayashi,
Heterocycles, 25, 205-211 (1987).


An Efficient and Extremely Mild Catalyst System, Combined Use of Trityl Chloride and Tin(II) Chloride, in the Aldol and Michael Reactions,
T. Mukaiyama, S. Kobayashi, M. Tamura, Y. Sagawa,
Chem. Lett., 1987, 491-494.


A Significant Substituent Effect on the Stereochemistry of the Trityl Salt-Catalyzed Michael Reaction,
T. Mukaiyama, M. Tamura, S. Kobayashi,
Chem. Lett., 1987, 743-746.


α,β-Unsaturated Orthoesters as Michael Acceptors. The Trityl Salt-catalyzed Michael Reaction of α,β-Unsaturated Orthoesters with Silyl Enol Ethers,
S. Kobayashi, T. Mukaiyama,
Chem. Lett., 1987, 1183-1186.

The Michael Reaction of Various Quinones with Silyl Enol Ethers.A Facile Method for the Preparation of Benzofuran and Indole Derivatives,
T. Mukaiyama, Y. Sagawa, S. Kobayashi,
Chem. Lett., 1987, 2169-2172.


A Convenient Synthesis of C-α-D-Ribofuranosyl Compounds from 1-O-Acetyl-2,3,5-tri-O-benzyl-β-D-Ribose by the Promotion of Triphenylmethyl Perchlorate,
T. Mukaiyama, S. Kobayashi,
Carbohydr. Res., 171, 81-87 (1987).


The Stereoselective Michael Reaction of α,β-Unsaturated Thioesters with Silyl Ethers Promoted by Combined Use of Antimony(V) Chloride and Tin(II) Triflate,
S. Kobayashi, M. Tamura, T. Mukaiyama,
Chem. Lett., 1988, 91-94.


The Addition Reaction of Acetals to Activated Olefins under Extremely Mild Conditions,
T. Mukaiyama, K. Wariishi, Y. Saito, M. Hayashi, S. Kobayashi,
Chem. Lett., 1988, 1101-1104.


The Regioselective Addition Reaction of 1,2-Benzoquinones with Silyl Enol Ethers Catalyzed by Trityl Perchlorate,
Y. Sagawa, S. Kobayashi, T. Mukaiyama,
Chem. Lett., 1988, 1105-1108.


Substitution Reaction of Ketene Dithioacetals with Carbon Electrophiles by the Promotion of Trityl Chloride-Tin(II) Chloride or Trimethylsilyl Chloride-Tin(II) Chloride Catalyst System,
T. Mukaiyama, H. Sugumi, H. Uchiro, S. Kobayashi,
Chem. Lett., 1988, 1291-1294.


Trityl Salt Catalyzed Aldol Reaction between α,β-Acetylenic Ketones and Silyl Enol Ethers,
Kobayashi, S. Matsui, T. Mukaiyama,
Chem. Lett., 1988, 1491-1494.


Facile Synthesis of γ,δ-Unsaturated β-Azido Carbonyl Compounds via Successive Nucleophilic Additions on Cinnamaldehyde Dimethyl Acetal Catalyzed by Trityl Hexachloroantimonate,
T. Mukaiyama, P. Leon, S. Kobayashi,
Chem. Lett., 1988, 1495-1496.


Possible Mechanism for the Stereoselective Double Michael Reaction Catalyzed by Trityl Perchlorate,
S. Kobayashi, Y. Sagawa, H. Akamatsu, T. Mukaiyama,
Chem. Lett., 1988, 1777-1780.


Stereoselective 1,2-cis Glycosylation Reaction of 1-O-Acetylribose with Silylated Nucleophiles by the Promotion of a New Catalyst System,
T. Mukaiyama, T. Shimpuku, T. Takashima, S. Kobayashi,
Chem. Lett., 1989, 145-148.


Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes Promoted by the Combined Use of Chiral Diamine Coordinated Tin(II) Triflate and Tributyltin Fluoride,
S. Kobayashi, T. Mukaiyama,
Chem. Lett., 1989, 297-300.


Perfect Stereochemical Control in the Synthesis of syn-α-Methyl-β-hydroxy Thioesters by Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes,
T. Mukaiyama, H. Uchiro, S. Kobayashi,
Chem. Lett., 1989, 1001-1004.


The Addition Reaction of Acetals (Aldehydes) to Simple Olefins by the Use of a New Catalyst System, T. Mukaiyama, K. Wariishi, M. Furuya, S. Kobayashi,
Chem. Lett., 1989, 1277-1280.


Asymmetric Aldol-type Reaction between Both Achiral Ketene Silyl Acetals and Aldehydes by the Use of a Chiral Promoter,
S. Kobayashi, T. Sano, T. Mukaiyama,
Chem. Lett., 1989, 1319-1322.


Reductive Cross Coupling Reaction of a Glyoxylate with Carbonyl Compounds. A Facile Synthesis of α,β-Dihydroxycarboxylate Based on a Low Valent Titanium Compound,
T. Mukaiyama, H. Sugimura, T. Ohno, S. Kobayashi,
Chem. Lett., 1989, 1401-1404.


An Efficient Chiral Promoter in the Aldol-type Reaction. Chiral Diamine Coordinated Tin(II) Triflate-Dibutyltindiacetate Complex,
T. Mukaiyama, H. Uchiro, S. Kobayashi,
Chem. Lett., 1989, 1757-1760.


A Highly Enantioselective Synthesis of 2-Substituted Malates by Asymmetric Aldol Reaction,
S. Kobayashi, Y. Fujishita, T. Mukaiyama,
Chem. Lett., 1989, 2069-2072.