311778-87-7Relevant articles and documents
Diastereoselective sp3C-O Bond Formation via Visible Light-Induced, Copper-Catalyzed Cross-Couplings of Glycosyl Bromides with Aliphatic Alcohols
Dickson, Jalen L.,Loka, Ravi S.,Luo, Long,Nguyen, Hien M.,Schaugaard, Richard N.,Schlegel, H. Bernhard,Xu, Hengfu,Yu, Fei
, p. 5990 - 6001 (2020/07/04)
Copper-catalyzed cross-coupling reactions have become one of the most powerful methods for generating carbon-heteroatom bonds, an important framework of many organic molecules. However, copper-catalyzed C(sp3)-O cross-coupling of alkyl halides with alkyl
Environmentally benign β-stereoselective glycosidations of glycosyl phosphites using a reusable heterogeneous solid acid, montmorillonite K-10
Nagai, Hideyuki,Sasaki, Kaname,Matsumura, Shuichi,Toshima, Kazunobu
, p. 337 - 353 (2007/10/03)
Environmentally benign and stereoselective β-glycosidations of glycopyranosyl phosphites and alcohols using a reusable heterogeneous solid acid, montmorillonite K-10, as an activator have been developed. By these glycosidations, β-gluco-, 2-deoxy-β-gluco-
Synthesis of the methyl glycosides of a Di- and two trisaccharide fragments specific for the Shigella flexneri Serotype 2a O-antigen
Mulard, Laurence A.,Costachel, Corina,Sansonetti, Philippe J.
, p. 849 - 877 (2007/10/03)
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