Total Synthesis of Two Furanomycin Stereoisomers

DOI: 10.1021/jo00184a020

Source and publish data:

Journal of Organic Chemistry p. 1769 - 1772 (1984)

Update date:2022-08-03

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Authors:

Chen, Shin-Yih

Joullie, Madeleine M.

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Article abstract of DOI:10.1021/jo00184a020

D-Glucosamine hydrochloride (3), an inexpensive, commercially available reagent, has been transformed stereoselectively into two new stereoisomers of furanomycin, (αR,2S,5R)-furanomycin (2a) and its isomer with the opposite configuration at the amino acid

Full text of DOI:10.1021/jo00184a020

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