Issue 3, 1989

Short efficient synthesis of the α-L-fucosidase inhibitor, deoxyfuconojirimycin [1,5-dideoxy-1,5-imino-L-fucitol] from D-lyxonolactone

Abstract

The only protection required in a five-step synthesis of the α-L-fucosidase inhibitor, deoxyfuconojirimycin [1,5-dideoxy-1,5-imino-L-fucitol] from D-lyxonolactone, a readily available chiral pool material, is a single isopropylidene group.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 665-666

Short efficient synthesis of the α-L-fucosidase inhibitor, deoxyfuconojirimycin [1,5-dideoxy-1,5-imino-L-fucitol] from D-lyxonolactone

G. W. J. Fleet, S. Petursson, A. L. Campbell, R. A. Mueller, J. R. Behling, K. A. Babiak, J. S. Ng and M. G. Scarosc, J. Chem. Soc., Perkin Trans. 1, 1989, 665 DOI: 10.1039/P19890000665

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