111192-41-7Relevant academic research and scientific papers
A convenient iodonium-ion-assisted synthesis of an immunologically active tetrameric β(1->5)-linked D-galactofuranoside from the extracellular polysaccharide of Aspergillus and Penicillium species
Zuurmond, H. M.,Klein, P. A. M. van der,Veeneman, G. H.,Boom, J. H. van
, p. 437 - 441 (2007/10/02)
The non-terminal glycosyl donor, ethyl 2,3-di-O-benzoyl-5-O-(chloroacetyl)-6-O-pivaloyl-1-thio-α-D-galactofuranoside, could be used, with the promotor N-iodosuccinimide and catalytic trifluoromethanesulfonic acid, for the preparation of β-D-galf-(1->5)-β-
SYNTHESIS OF A CELL-WALL COMPONENT OF ASPERGILLUS NIGER CONTAINING FOUR β(1-5)-interlinked D-GALACTOFURANOSYL RESIDUES
Veeneman, G. H.,Hoogerhout, P.,Westerduin, P.,Notermans, S.,Boom, J. H. van
, p. 129 - 131 (2007/10/02)
The derivative 2,3-di-O-benzoyl-5-O-chloroacetyl-6-O-pivaloyl-β-D-galactofuranosyl chloride proved to be very suitable for the introduction, via the Helferich procedure, of three β(1-5) interlinked D-galactofuranosyl residues and a β-orientated spacer.
