1033706-52-3Relevant academic research and scientific papers
Chemical synthesis of cyclic galactooligofuranosides isolated from enzymatic degradation products of cell wall arabinogalactan of Mycobacterium tuberculosis
Kwan, Soo Kim,Lee, Bo-Young,Sung, Ho Yoon,Hyo, Jin Jeon,Ju, Yuel Baek,Jeong, Kyu-Sung
supporting information; experimental part, p. 2373 - 2376 (2009/05/27)
(Chemical Equation Presented) Synthesis of cyclic tetra-, hexa- and octasaccharides containing alternating (1→5)-β- and (1→6)-β-galactofuranosyl linkages has been achieved by intramolecular cycloglycosylation of corresponding linear sugars and by cyclooligomerization of 1,6-linked and 1,5-linked disaccharides. In particular, cyclooligomerization of the (1→6)-β-galactofuranosyl disaccharide provides an efficient way to secure all three cyclic sugars in one operation.
