Synthesis of a biotinylated penta-α-(1→6)-d-glucoside based on the rational design of an α-stereoselective glucosyl donor?

Organic Chemistry Frontiers Pub Date: 2017-12-04 DOI: 10.1039/C7QO01007A

Abstract

Two glucosyl donors, which allowed for the α-selective glucosylation of primary hydroxyl groups, were designed using a combination of acyl groups capable of remote participation, an electron-withdrawing pentafluorobenzoyl substituent and a bulky TBDPS protecting group. The first had a participating levulinoyl group at O-3 and the TBDPS protecting group at O-6, and the second bore an acetyl group at O-3 and the pentafluorobenzoyl one at O-6. With the help of these donors, two synthetic schemes, convergent and linear, towards a pentaglucoside representing the α-(1→6)-linked glucans of Helicobacter pylori were evaluated. The linear scheme proved to be preferential over the convergent one because of its insufficiently high α-stereoselectivity demonstrated by disaccharide donors. For the linear scheme, the pentafluorobenzoyl group turned out to be more convenient than TBDPS at the removal step. The α-(1→6)-linked pentaglucoside was prepared by iteration of glucosylation with the donor bearing 3-O-acetyl and 6-O-pentafluorobenzoyl and the subsequent liberation of the 6-OH group. Biotin was attached to the pentaglucoside via the spacer amino group.

Graphical abstract: Synthesis of a biotinylated penta-α-(1→6)-d-glucoside based on the rational design of an α-stereoselective glucosyl donor
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