Merck
CN

Synthesis of neutral glycosphingolipids from Zygomycetes.

Carbohydrate research (2008-06-07)
Noriyasu Hada, Junko Oka, Kyoko Hakamata, Kenji Yamamoto, Tadahiro Takeda
ABSTRACT

Novel neutral glycosphingolipids (NGSLs) containing Gal-alpha1-->6Gal, previously found in the Zygomycetes species Mucor hiemalis, were synthesized. The structures of these compounds are different from those of other fungal GSLs, and they are expected to be involved in host-parasite interactions. A key step in their synthesis is direct 1,2-cis alpha-selective galactosylation of 4,6-diol tri- and tetrasaccharide acceptors with a galactosyl donor in the presence of N-iodosuccinimide (NIS)/trifluoromethanesulfonic acid (TfOH). The fully protected glycosides were deprotected to give the two target glycosphingolipids.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
N-Iodosuccinimide, 95%