Synthesis of sialyl Lewis X ganglioside analogs containing a variable length spacer between the sugar and lipophilic moieties

Article abstract of DOI:10.1080/07328309808002340

Five sialyl Lewis X ganglioside analogs containing 4-(2-tetradecylhexadecanoylamino)benzyl group in place of ceramide and a variety of lengths of ethylene glycol chains as the spacer, have been synthesized. Glycosidation of O-(methyl 5-acetamido-4,7,8,9-t

Full text of DOI:10.1080/07328309808002340

Journal of Carbohydrate Chemistry
ISSN: 0732-8303 (Print) 1532-2327 (Online) Journal homepage: http://www.tandfonline.com/loi/lcar20
Synthesis of Sialyl Lewis X Ganglioside Analogs
Containing A Variable Length Spacer Between the
Sugar and Lipophilic Moieties
Keisuke Adachi , Yutaka Yamada , Hiroaki Wada , Akihiko Kameyama ,
Hideharu Ishida & Makoto Kiso
To cite this article: Keisuke Adachi , Yutaka Yamada , Hiroaki Wada , Akihiko Kameyama ,
Hideharu Ishida & Makoto Kiso (1998) Synthesis of Sialyl Lewis X Ganglioside Analogs
Containing A Variable Length Spacer Between the Sugar and Lipophilic Moieties , Journal of
Carbohydrate Chemistry, 17:4-5, 595-607
To link to this article: http://dx.doi.org/10.1080/07328309808002340
Published online: 22 Aug 2006.
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Date: 08 June 2016, At: 21:19