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Published on: November 8, 2016
On the generality of the superarmament of glycosyl donors
Lulu Teressa Poulsen1, Mads Heuckendorff, Henrik H Jensen
1Department of Chemistry, Aarhus University, Langelandsgade 140, 8000 Aarhus C, Denmark. hhj@chem.au.dk.
Abstract:
It was established that 2-O-benzoyl-3,4,6-tri-O-benzyl protected β-SEt, β-SPh and β-SBox glucosyl donors are not superarmed when using the NIS/TfOH promoter system, but instead have a similar reactivity as their classically armed tetra-O-benzyl protected glucosyl counterparts. The β-SBox 2-O-benzoyl-3,4,6-tri-O-benzyl glucosyl donor, however, was found to be superarmed under DMTST activation. Our studies have shown that the increased reactivity of the β-SBox 2-O-benzoyl-3,4,6-tri-O-benzyl glucosyl donor with DMTST activation could be a unique case, and that the high reactivity of glucosyl donors with the 2-O-benzoyl-3,4,6-tri-O-benzyl protection pattern is not general as earlier suggested.
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