869216-48-8Relevant articles and documents
Arabinofuranose 1,2,5-orthobenzoate as a single precursor of linear α(1 → 5)-linked oligoarabinofuranosides
Panova, Maria V.,Podvalnyy, Nikita M.,Okun, Eugene L.,Abronina, Polina I.,Chizhov, Alexander O.,Kononov, Leonid O.
, p. 35 - 44 (2017/12/26)
Selectively protected mono-, di- and trisaccharide thioglycoside building blocks with unprotected primary hydroxy group at the non-reducing end, available in only one step from 3-O-benzoyl β-D-arabinofuranose 1,2,5-orthobenzoate, were used in the synthesis of linear α(1 → 5)-linked oligoarabinofuranosides up to octasaccharide. The obtained oligosaccharides contain 4-(2-chloroethoxy)phenyl (CEP) or 4-(2-azidoethoxy)phenyl (AEP) pre-spacer aglycons that allow preparation of neoglycoconjugates.
Ring opening of acylated β-d-arabinofuranose 1,2,5-orthobenzoates with nucleophiles allows access to novel selectively-protected arabinofuranose building blocks
Podvalnyy, Nikita M.,Sedinkin, Sergey L.,Abronina, Polina I.,Zinin, Alexander I.,Fedina, Ksenia G.,Torgov, Vladimir I.,Kononov, Leonid O.
, p. 7 - 15 (2011/02/26)
β-d-Arabinofuranose 1,2,5-orthobenzoates with 3-O-acetyl, 3-O-benzoyl, and 3-O-chloroacetyl groups were prepared in an efficient manner starting from readily available crystalline methyl 2,3,5-tri-O-benzoyl-α-d- arabinofuranoside, and ring-opening reactio
Efficient one-pot syntheses of α-d-arabinofuranosyl tri- and tetrasaccharides present in cell wall polysaccharide of Mycobacterium tuberculosis
Liang, Xing-Yong,Deng, Li-Min,Liu, Xia,Yang, Jin-Song
scheme or table, p. 87 - 93 (2010/02/28)
Two α-d-arabinofuranosyl oligosaccharides (2 and 3) found as constituent parts of the polysaccharide portion from the cell wall of Mycobacterium tuberculosis have been efficiently synthesized via a one-pot glycosylation procedure in which a key step is th
An efficient synthesis of a dimer of the tetrasaccharide present in motif B of the Mycobacterium tuberculosis cell wall
Mei, Xiangdong,Ning, Jun
, p. 2267 - 2272 (2007/10/03)
An efficient method for the synthesis of 3,5-branched octaarabinoside, which is a dimer of the tetrasaccharide present in motif B of the Mycobacterium tuberculosis cell wall, has been developed by using 2,3,5-tri-O-benzoyl-α- D-arabinofuranosyl trichloroa