Synthesis of a new potent α-fucosidase inhibitor

DOI: 10.1039/CC9960002649

Source and publish data:

Chemical Communications p. 2649 - 2650 (1996)

Update date:2022-07-29

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Authors:

Hansen, Anja

Tagmose, Tina M.

Bols, Mikael

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Article abstract of DOI:10.1039/CC9960002649

Enantiomerically pure (3S,4R,5R)-3,4-dihydroxy-5-methylpiperidine was prepared from L-arabinose and found to be a potent human placenta α-fucosidase inhibitor.

Full text of DOI:10.1039/CC9960002649

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