Koki Matsubara

An Efficient Glycosylation Reaction of 1-Hydroxy Sugars with Various Nucleophiles Using A Catalytic Amount of Activator and Hexamethyldisiloxane

Teruaki Mukaiyama, Koki Matsubara, Miyuki Hora · Synthesis · 1994 · 41 citations

Engineering, Glycobiology, Glycosylation Reactions +16

Stereoselective Glycosylation Reaction Starting from 1-O-Trimethylsilyl Sugars by Using Diphenyltin Sulfide and a Catalytic Amount of Active Acidic Species

Teruaki Mukaiyama, Koki Matsubara · Chemistry Letters · 1992 · 38 citations

Bioorganic Chemistry, Engineering, Glycobiology +18

An Efficient Method for the Stereoselective Synthesis of 1,2-<i>cis</i>- and 1,2-<i>trans</i>-Ribofuranosides from 1-Hydroxy Ribofuranose by the Use of Diphenyltin Sulfide and Trifluoromethanesulfonic Anhydride

Teruaki Mukaiyama, Koki Matsubara, Shinji Suda · Chemistry Letters · 1991 · 25 citations

Halogenation, Diphenyltin Sulfide, Bioorganic Chemistry +11

High-Yielding Catalytic Synthesis of Glycosyl Azides from Peracylated Sugars

Koki Matsubara, Teruaki Mukaiyama · Chemistry Letters · 1994 · 19 citations

Glycosyl Azides, Chemical Engineering, Engineering +14

Catalytic Stereoselective Synthesis of α- or β-Glucosides Using a Single Glycosyl Donor, 1-O-2′-(2′-Methoxyethoxy)acetyl-Glucopyranose Derivative

Koki Matsubara, Takenori Sasaki, Teruaki Mukaiyama · Chemistry Letters · 1993 · 16 citations

Engineering, Glycobiology, Organic Chemistry +16