Stereoselective Preparation of β-C-Glycosides from 2-Deoxyribose Utilizing Neighboring Participation by 3-O-Methylsulfinylethyl Group

DOI: 10.1246/cl.1987.2139

Source and publish data:

Chemistry Letters p. 2139 - 2142 (1987)

Update date:2022-08-03

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Authors:

Narasaka, Koichi

Ichikawa, Yuh-ichiro

Kubota, Hideki

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Article abstract of DOI:10.1246/cl.1987.2139

Acid catalyzed reaction of 2-deoxy-3-O-methylsulfinylethylribofuranosyl acetate with silyl enol ethers proceeded stereoselectively, resulting in the predominant formation of the corresponding β-C-glycosides.

Full text of DOI:10.1246/cl.1987.2139

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