STRUCTURAL ELUCIDATION OF A NEUTRAL WATER-SOLUBLE α-D-GLUCAN FROM THE FUNGUS OF HERICIUM ERINACEUS

2011 ◽  
Vol 35 (6) ◽  
pp. 1680-1685 ◽  
Author(s):  
ANQIANG ZHANG ◽  
YINGLIN DENG ◽  
PEILONG SUN ◽  
XIANGHE MENG ◽  
JINGSONG ZHANG
2020 ◽  
Author(s):  
Ian Sims ◽  
CJ Pollock ◽  
R Horgan

Individual fructan tri-, tetra- and pentasaccharide isomers in neutral, water-soluble extracts from Lolium temulentum were purified and the linkages present in these isomeric oligosaccharides were analysed by combined GC-mass spectrometry of partially methylated alditol acetates. 1-Kestose and neokestose were the most abundant trisaccharides with 6-kestose present in much lower amounts. Analysis of isomers of DP 4 and 5 showed that multiple linkage types were present with structures based on all three trisaccharides. Oligosaccharides based on neokestose but with 2,6 linkages between adjacent fructose residues have not been previously detected in higher plants. © 1992.


2007 ◽  
Vol 40 (6) ◽  
pp. 2201-2209 ◽  
Author(s):  
N. Yoshinaga ◽  
D. J. Bicout ◽  
E. I. Kats ◽  
A. Halperin

RSC Advances ◽  
2020 ◽  
Vol 10 (45) ◽  
pp. 26717-26727
Author(s):  
Federica Battistin ◽  
Alessio Vidal ◽  
Gabriele Balducci ◽  
Enzo Alessio

The reactivity of selected Ru(ii)-PTA carbonyls with potentially labile ligands (i.e. H2O, dmso and/or Cl) towards the model imine ligands pyridine and 2,2′-bipyridine was investigated, yielding several neutral and cationic water-soluble derivatives.


2001 ◽  
Vol 84 (8) ◽  
pp. 2398-2408 ◽  
Author(s):  
Jing Wang ◽  
Filip Meersman ◽  
Robert Esnouf ◽  
Matthias Froeyen ◽  
Roger Busson ◽  
...  

2015 ◽  
Vol 112 (22) ◽  
pp. 6882-6886 ◽  
Author(s):  
Cyrille Costentin ◽  
Marc Robert ◽  
Jean-Michel Savéant ◽  
Arnaud Tatin

Substitution of the four paraphenyl hydrogens of iron tetraphenylporphyrin by trimethylammonio groups provides a water-soluble molecule able to catalyze the electrochemical conversion of carbon dioxide into carbon monoxide. The reaction, performed in pH-neutral water, forms quasi-exclusively carbon monoxide with very little production of hydrogen, despite partial equilibration of CO2 with carbonic acid—a low pKa acid. This selective molecular catalyst is endowed with a good stability and a high turnover frequency. On this basis, prescribed composition of CO–H2 mixtures can be obtained by adjusting the pH of the solution, optionally adding an electroinactive buffer. The development of these strategies will be greatly facilitated by the fact that one operates in water. The same applies for the association of the cathode compartment with a proton-producing anode by means of a suitable separator.


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