Journal
ORGANIC LETTERS
Volume 25, Issue 16, Pages 2788-2792Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c00670
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Highly stereoselective construction of 1,2-cis-Arap linkages has been achieved with a broad range of alcoholic acceptors, including strong nucleophiles and complex bioactive molecules. This method was applied to a regioselective and orthogonal one-pot synthesis of a pentasaccharide, which serves as the structural motif of a side chain in type II arabinogalactan.
Highly stereoselective construction of 1,2-cis-Arap linkages has been achieved, which featured a broad range of alcoholic acceptors, including strong nucleophiles and complex bioactive molecules. This method was applied to a regioselective and orthogonal one-pot synthesis of a pentasaccharide, which was the structural motif of a side chain in type II arabinogalactan.
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