C-Nucleosides. 6. Synthesis of 5-Methoxy-5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan-2(5H)-one and Its Ring Transformation

DOI: 10.1021/jo00229a017

Source and publish data:

Journal of Organic Chemistry p. 4521 - 4526 (1987)

Update date:2022-08-04

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Authors:

Maeba, Isamu

Suzuki, Makoto

Hara, Osamu

Takeuchi, Tomohiko

Iijima, Takashi

Furukawa, Hiroshi

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Article abstract of DOI:10.1021/jo00229a017

Synthesis of the versatile and stable C-nucleoside precursor 5-hydroxy-5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan-2(5H)-one (2) was achieved by oxidation of glycosyl furan (1) with Jones reagent.Treatment of 2 with triethylamine in benzene afforded th

Full text of DOI:10.1021/jo00229a017

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