Literature DB >> 7697656

Improved synthesis of glycosylamines and a straightforward preparation of N-acylglycosylamines as carbohydrate-based detergents.

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.

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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


  2 in total

1.  Glycosylated self-assembled monolayers for arrays and surface analysis.

Authors:  Fang Cheng; Daniel M Ratner
Journal:  Methods Mol Biol       Date:  2012

2.  Ammoxidation of lignocellulosic materials: formation of nonheterocyclic nitrogenous compounds from monosaccharides.

Authors:  Karl Michael Klinger; Falk Liebner; Takashi Hosoya; Antje Potthast; Thomas Rosenau
Journal:  J Agric Food Chem       Date:  2013-09-10       Impact factor: 5.279

  2 in total

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