| Literature DB >> 7697656 |
A Lubineau1, J Augé, B Drouillat.
Abstract
D-Glucose, D-galactose, lactose, cellobiose, and maltose yield quantitatively the corresponding glycosylamine when treated at 42 degrees C for 36 h with a commercial aqueous solution of ammonia in the presence of one equivalent of ammonium hydrogen carbonate. After lyophilisation, the residue (i.e., the pure glucosylamine) was dissolved in a mixture of ethanol and water, and treated with acyl chlorides to afford in a few minutes N-acylglucosylamines. Micellar properties of these amphiphilic derivatives were determined.Entities:
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Year: 1995 PMID: 7697656 DOI: 10.1016/0008-6215(94)00275-k
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104