Stereoselective Oxylactonization. Preparation of 2-Deoxy-DL-ribono-1,4-lactone Derivatives from 3-Silyloxy-4-alkenamides

DOI: 10.1246/bcsj.58.3309

Source and publish data:

Bulletin of the Chemical Society of Japan p. 3309 - 3311 (1985)

Update date:2022-08-10

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Authors:

Ichikawa, Yuch-ichiro

Miwa, Tetsuo

Narasaka, Koichi

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Article abstract of DOI:10.1246/bcsj.58.3309

The oxylactonization of 3-silyloxy-4-alkenamides proceeds stereoselectively by treatment with m-chloroperbenzoic acid to give the corresponding 2-deoxy-DL-ribono-1,4-lactone derivatives.

Full text of DOI:10.1246/bcsj.58.3309

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