Title of article
Synthesis of neutral glycosphingolipids from Zygomycetes
Author/Authors
Noriyasu Hada، نويسنده , , Junko Oka، نويسنده , , Kyoko Hakamata، نويسنده , , Kenji Yamamoto، نويسنده , , Tadahiro Takeda، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2008
Pages
10
From page
2315
To page
2324
Abstract
Novel neutral glycosphingolipids (NGSLs) containing Gal-α1→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 α-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.
Keywords
Zygomycetes species , ?-Galactosylation , 1 , 2-cis-Glycoside , Mucor hiemalis , Di-tert-butylsilylene group
Journal title
Carbohydrate Research
Serial Year
2008
Journal title
Carbohydrate Research
Record number
965551
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