| Literature DB >> 12433464 |
Anneke M van der Heijden1, Tsz Chung Lee, Fred van Rantwijk, Herman van Bekkum.
Abstract
Glycosidation of saccharides combines the essential characteristics of two major renewable classes, viz. triglycerides and carbohydrates, leading to biofriendly surfactants and emulsifiers. The development of the alkylglycosides derived from reducing disaccharides has lagged, because no efficient synthesis was available. We have found that ordered mesoporous materials of the MCM-41 type are active and selective catalysts for the glycosidation of disaccharides containing fructose at the reducing end, i.e., isomaltulose, lactulose and leucrose. No alcoholysis or hydrolysis of the glycosidic bond was observed, demonstrating the mildness of the MCM-41 catalyst. Leucrose was found to be less reactive than the two other disaccharides, in accordance with the absence of furanose forms in leucrose. Copyright 2002 Elsevier Science Ltd.Entities:
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Year: 2002 PMID: 12433464 DOI: 10.1016/s0008-6215(02)00171-4
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104