Biology; Chemistry and chemical biology; Chemical and biological engineering; Biomedical engineering
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Regioselective Synthesis of Sucrose Monoesters as Surfactants,I. R. Vlahov, P. I. Vlahova, R.J. Linhardt, Journal of CarbohydrateChemistry, 16, 1-10, 1997.
A highly regioselective conversion of sucrose into 6-O-acyl derivatives is reported. First sucrose was transformed into the dibutyltin acetal, thus enhancing the nucleophilicity at the C-6 oxygen and restricting the subsequent acylation reaction. The surface activity properties of the sucrose monoesters obtained were determined and compared with those of commercially available ionic and non-ionic surfactants.;
Journal of Carbohydrate Chemistry, 16, 1-10; Note : if this item contains full text it may be a preprint, author manuscript, or a Gold OA copy that permits redistribution with a license such as CC BY. The final version is available through the publisher’s platform.
The Linhardt Research Labs.; The Shirley Ann Jackson, Ph.D. Center for Biotechnology and Interdisciplinary Studies (CBIS);
The Linhardt Research Labs Online Collection; Rensselaer Polytechnic Institute, Troy, NY; Journal of Carbohydrate Chemistry; https://harc.rpi.edu/;