A new synthesis of (+)-cyclophellitol, a potent β-glucosidase inhibitor, has been completed in nine steps from D-xylose. The key transformations involve a zinc-mediated fragmentation of benzyl-protected methyl 5-deoxy-5-iodo-xylofuranoside followed by a h
Hansen, Flemming Gundorph,Bundgaard, Eva,Madsen, Robert
p. 10139 - 10142
(2007/10/03)
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