Stereoselective β-C- and β-S-Glycosylation of 2-Deoxyribofuranose Derivatives Controlled by the 3-Hydroxy Protective Group

DOI: 10.1246/bcsj.62.845

Source and publish data:

Bulletin of the Chemical Society of Japan p. 845 - 852 (1989)

Update date:2022-07-29

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Authors:

Ichikawa, Yuh-ichiro

Kubota, Hideki

Fujita, Ken'ichi

Okauchi, Tatsuo

Narasaka, Koichi

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Article abstract of DOI:10.1246/bcsj.62.845

β-C-2-Deoxyribofuranosides and β-S-2-deoxyribofuranosides are prepared stereoselectively from 1-O-acetyl-5-O-benzyl-3-O-<2-(methylsulfinyl)ethyl>-2-deoxy-D-erythro-pentofuranose or the corresponding 3-O-(2-pyridylmethyl)pentofuranose N-oxide by the reacti

Full text of DOI:10.1246/bcsj.62.845

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