Stereocontrolled Route to 3-Amino-2,3,6-trideoxy-hexopyranoses. K-10 Montmorillonite as a Glycosidation Reagent for Acosaminide Synthesis

DOI: 10.1039/c39870001171

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1171 - 1172 (1987)

Update date:2022-09-26

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Authors:

Florent, Jean-Claude

Monneret, Claude

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Article abstract of DOI:10.1039/c39870001171

A stereoselective synthesis of methyl .(or benzyl) 3-azido-2,3,6-trideoxy-α-L-arabino-hexopyranoside from di-O-acetyl-L-rhamnal is reported; it proceeds via addition of hydrazoic acid to a hex-2-enopyranose, followed by acetylation and glycosidation with

Full text of DOI:10.1039/c39870001171

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