159922-50-6Relevant articles and documents
Total synthesis of sulfated glycosphingolipid SM1a, a kind of human epithelial carcinoma antigen
Zhang, Pengtao,Wang, Kun,Zhang, Jun,Li, Chunxia,Guan, Huashi
, p. 570 - 583 (2015/01/30)
A highly efficient and practical total synthesis of the sulfated ganglioside SM1a, a kind of human epithelial carcinoma antigen identified in mammalian kidney, has been accomplished for the first time. The characteristic sequence of SM1a, β-D-Galp-(1→3)-β
Chemical synthesis of a tetrasaccharide related to the exocellular polysaccharide from Rhodococcus sp. RHA1
Budhadev, Darshita,Mukhopadhyay, Balaram
, p. 26 - 31 (2014/07/08)
Chemical synthesis of the tetrasaccharide related to the exocellular polysaccharide from Rhodococcus sp. RHA1 is reported. The stereoselective glycosylations were achieved by activation of the thioglycoside donors using N-iodosuccinimide in the presence of La(OTf)3 varying temperature per the need of 1,2-cis or 1,2-trans glycosylations. The target tetrasaccharide is reported in the form of its p-methoxyphenyl glycoside that can be cleaved selectively from the per-O-acetylated derivative allowing further glycoconjugate formation using trichloroacetimidate chemistry.
Synthesis of some blocked di- and trisaccharide derivatives related to the repeating unit of the O-antigen from Shigella dysenteriae type 3 in the form of their glycosides
Sarkar, Sujit Kumar,Roy, Nirmolendu
, p. 2386 - 2394 (2007/10/03)
Starting from D-galactose and D-galactosamine hydrochloride, two new monosaccharide synthons namely 2-(trimethylsilyl)ethyl 4-O-acetyl-2,6-di-O- benzyl-β-D-galactopyranoside 2 and phenyl 3-O-acetyl-4,6-O-benzylidene-2- deoxy-2-phthalimido-1-thio-β-D-galac
Efficient synthesis of two HNK-1 related pentasaccharides
Belot, Frederic,Otter, Albin,Fukuda, Minoru,Hindsgaul, Ole
, p. 1315 - 1318 (2007/10/03)
Two pentasaccharides, representative of those found on complex N-glycans, were synthesized for use as potential substrates for sulfotransferases. The synthesis was achieved by the addition of a disaccharide donor β-D-GlcA(1→3)α-D-Gal-trichloroacetimidate
SYNTHESIS OF HUMAN M BLOOD GROUP ANTIGENIC GLYCOPEPTIDE
Nakahara, Yoshiaki,Iijima, Hiroyuki,Ogawa, Tomoya
, p. 3321 - 3324 (2007/10/02)
A first total synthesis of terminal glycoheptapeptide of human glycophorin AM was accomplished by solution phase peptide condensation utilizing the tetrasaccharide-linked amino acid building blocks designed for Fmoc strategy.