6-Nitro-2-benzothiazolyl α-Glucoside and α-Mannoside in β-Selective Glycosylations
スポンサーリンク
概要
著者
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Mukaiyama Teruaki
Center For Basic Research The Kitasato Institute (tci)
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Mandai Hiroki
Center For Basic Research The Kitasato Institute (tci)
関連論文
- 6-Nitro-2-benzothiazolyl α-Glucoside and α-Mannoside in β-Selective Glycosylations
- 6-Nitro-2-benzothiazolyl α-Glucoside and α-Mannoside in β-Selective Glycosylations
- Catalytic and β-Stereoselective Mannosylation of Several Glycosyl Acceptors with Mannosyl 6-Nitro-2-benzothiazoate
- Glycosyl 6-Nitro-2-benzothiazoate. A Highly Efficient Donor for β-Stereoselective Glycosylation
- Protic Acid Catalyzed Stereoselective Glycosylation Using Glycosyl Fluorides
- A Catalytic and α-Selective Sialylation Using Novel 5-Azido Sialy Fluoride
- A Catalytic and Stereoselective Glycosylation with Glucopyranosyl Fluoride by Using Various Protic Acids
- A New Method for α-Selective Glycosylation Using a Donor, Glycosyl Methyldiphenylphosphonium Iodide, without Any Assistance of Acid Promoters
- 6-Nitro-2-benzothiazolyl α-Mannoside : A Highly Efficient Mannosyl Donor in Constructing β-Man(1→4)GlcN Linkage and Its Application to the Synthesis of the Pentasaccharide Core of N-Glycans
- Efficient and Concise Synthesis of βMan1-4GlcN Linkage of Pentasaccharide Core by Using 6-Nitro-2-benzothiazolyl α-Mannoside
- Glycosyl Phosphonium Halide as a Reactive Intermediate in Highly α-Selective Glycosylation