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Title: Synthesis of carbohydrate-based surfactants

Abstract

The present invention provides carbohydrate-based surfactants and methods for producing the same. Methods for producing carbohydrate-based surfactants include using a glycosylation promoter to link a carbohydrate or its derivative to a hydrophobic compound.

Inventors:
; ;
Issue Date:
Research Org.:
The Arizona Board of Regents on behalf of the University of Arizona, Tucson, AZ (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1333299
Patent Number(s):
9,499,575
Application Number:
14/041,251
Assignee:
The Arizona Board of Regents on behalf of the University of Arizona (Tucson, AZ)
DOE Contract Number:  
FG03-93ER61526
Resource Type:
Patent
Resource Relation:
Patent File Date: 2013 Sep 30
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES; 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY

Citation Formats

Pemberton, Jeanne E., Polt, Robin L., and Maier, Raina M. Synthesis of carbohydrate-based surfactants. United States: N. p., 2016. Web.
Pemberton, Jeanne E., Polt, Robin L., & Maier, Raina M. Synthesis of carbohydrate-based surfactants. United States.
Pemberton, Jeanne E., Polt, Robin L., and Maier, Raina M. Tue . "Synthesis of carbohydrate-based surfactants". United States. https://www.osti.gov/servlets/purl/1333299.
@article{osti_1333299,
title = {Synthesis of carbohydrate-based surfactants},
author = {Pemberton, Jeanne E. and Polt, Robin L. and Maier, Raina M.},
abstractNote = {The present invention provides carbohydrate-based surfactants and methods for producing the same. Methods for producing carbohydrate-based surfactants include using a glycosylation promoter to link a carbohydrate or its derivative to a hydrophobic compound.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {2016},
month = {11}
}

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Works referenced in this record:

Functions and potential applications of glycolipid biosurfactants — from energy-saving materials to gene delivery carriers —
journal, September 2002

  • Kitamoto, Dai; Isoda, Hiroko; Nakahara, Tadaatsu
  • Journal of Bioscience and Bioengineering, Vol. 94, Issue 3, p. 187-201
  • DOI: 10.1016/S1389-1723(02)80149-9

Rhamnolipid-Induced Removal of Lipopolysaccharide from Pseudomonas aeruginosa: Effect on Cell Surface Properties and Interaction with Hydrophobic Substrates
journal, August 2000


Chemical Synthesis of a Glycolipid Library by a Solid-Phase Strategy Allows Elucidation of the Structural Specificity of Immunostimulation by Rhamnolipids
journal, September 2006

  • Bauer, Jörg; Brandenburg, Klaus; Zähringer, Ulrich
  • Chemistry - A European Journal, Vol. 12, Issue 27
  • DOI: 10.1002/chem.200600482

New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs-Knorr Method? [New Synthetic Methods (56)]
journal, March 1986

  • Schmidt, Richard R.
  • Angewandte Chemie International Edition in English, Vol. 25, Issue 3, p. 212-235
  • DOI: 10.1002/anie.198602121

Glycosylation of sialyl acetates with a novel catalyst combination: Bismuth triflate and BF3·OEt2 system
journal, July 2003

  • Ikeda, Kiyoshi; Torisawa, Yasuhiro; Nishi, Takao
  • Bioorganic & Medicinal Chemistry, Vol. 11, Issue 14, p. 3073-3076
  • DOI: 10.1016/S0968-0896(03)00277-3

Glycosylation of sialyl acetates with a novel catalyst combination: Bismuth triflate and BF3·OEt2 system
journal, July 2003

  • Ikeda, Kiyoshi; Torisawa, Yasuhiro; Nishi, Takao
  • Bioorganic & Medicinal Chemistry, Vol. 11, Issue 14, p. 3073-3076
  • DOI: 10.1016/S0968-0896(03)00277-3

Bismuth(III) Triflate-Catalyzed Dehydrative Glycosidation Using 1- Hydroxy Sugars
journal, January 2008


Minimally Competent Lewis Acid Catalysts: Indium(III) and Bismuth(III) Salts Produce Rhamnosides (=6-Deoxymannosides) in High Yield and Purity
journal, December 2012

  • Coss, Clifford; Carrocci, Tucker; Maier, Raina M.
  • Helvetica Chimica Acta, Vol. 95, Issue 12
  • DOI: 10.1002/hlca.201200528