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Synthesis of a water-soluble serine-based neoglycolipid which can be covalently linked to solid phases

✍ Scribed by Mikael Elofsson; Johan Broddefalk; Tomas Ekberg; Jan Kihlberg


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
813 KB
Volume
258
Category
Article
ISSN
0008-6215

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✦ Synopsis


NO-Fmoc-serine pentafluorophenyl ester was glycosylated with perbenzoylated lactosyl bromide. The resulting product was coupled to a resin functionalized with 6aminohexanoic acid and then Na-acylated to give a serine-based analogue of lactosylceramide.

The water-soluble neoglycolipid was covalently linked to microtiter plates via its carboxyl group and was recognized by a lactose-binding lectin in an ELISA.