Affiliation:
1. Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-4330 Mülheim an der Ruhr
Abstract
Abstract
Stoichiometric reactions of 2,3:5,6-di-O-ethylboranediyl-α-D -mannofuranosyl bromide (1) with O -nucleophiles at room temperature give β-D-mannofuranosides with excellent stereoselectivities. The labile glycosides obtained are deboronated in quantitative yields and then converted to their tetra-O -acetates. The products are characterized by NMR spectroscopy.
Cited by
6 articles.
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