849420-02-6Relevant articles and documents
Efficient glycosylation with glycosyl ortho-allylbenzoates as donors
Liang, Haijing,Ma, Lixia,Li, Changwei,Peng, Qiang,Wang, Zhaoyan,Zhang, Zhan-xin,Yu, Lan,Liu, Huanxiang,An, Fengli,Xue, Weihua
supporting information, p. 84 - 87 (2018/11/30)
Glycosylation reactions are significant as they provide access to model compounds that are useful for elucidating biochemical pathways. Herein, we describe the development of glycosyl ortho-alkynylbenzoates as novel, bench-top stable, and readily availabl
"One-pot" access to α-d-mannopyranosides from glycals employing ruthenium catalysis
Chittela, Sravanthi,Reddy, Thurpu Raghavender,Krishna, Palakodety Radha,Kashyap, Sudhir
, p. 46327 - 46331 (2015/02/19)
Ru-catalyzed synthesis of α-d-mannopyranosides from glucal is described via one-pot glycosylation-dihydroxylation reaction. This method is amenable to a variety of acceptors, including carbohydrate-derived and amino-acid containing alcohols to obtain mannosylated peptides and disaccharides.
Synthesis and characterization of mannosylated oligoribonucleotides
Zhao, Yuyan,Tram, Kha,Yan, Hongbin
experimental part, p. 2137 - 2143 (2010/01/03)
Oligoribonucleotide (RNA)-carbohydrate conjugates bearing mono- and divalent mannosides were readily obtained using 3,4-diethoxy-3-cyclobutene-1,2-dione as the linking agent in the presence of trace amount of triethylamine. The glycoconjugates were purifi
