129796-68-5Relevant academic research and scientific papers
O-(p-Methoxyphenylethynyl)phenyl Glycosides: Versatile New Glycosylation Donors for the Highly Efficient Construction of Glycosidic Linkages
Hu, Yang,Yu, Ke,Shi, Li-Li,Liu, Lei,Sui, Jing-Jing,Liu, De-Yong,Xiong, Bin,Sun, Jian-Song
, p. 12736 - 12744 (2017)
A novel alkyne-activation-based glycosylation protocol using o-(p-methoxyphenylethynyl)phenyl (MPEP) glycoside was established. The glycosyl MPEP donors were shelf-stable and could be prepared efficiently via Sonogashira reaction from the corresponding o-
α-Selective thermal glycosidation of rhamnosyl and mannosyl chlorides
Nishizawa, Mugio,Kan, Yukiko,Shimomoto, Waka,Yamada, Hidetoshi
, p. 2431 - 2434 (2007/10/02)
Stereoselective thermal glycosylation of a variety of alcohols with 2,3,4-tri-O-benzylα-L-rhamnopyranosyl chloride and 2,3,4,6-tstra-O-benzyl-α-D-mannopyranosyl chloride have achieved to give α-glycosides in high selectivity.
