866552-44-5Relevant academic research and scientific papers
An efficient synthetic route to O-(2-O-benzyl-3,4-di-O-acetyl-α/β-L-fucopyranosyl)-trichloroacetimidate
Tolón Murguía, Blanca I.,Iglesias Morales, Yuleidys de las Mercedes,Mesa Hernández, Miriam,Yu Pérez, Yaneisy,Labrada Regalado, Claudia,Garrido Arteaga, Raine,Paquet, Fran?oise,López López, Miguel A.
, (2020/12/29)
An efficient synthetic route to prepare O-(2-O-benzyl-3,4-di-O-acetyl-α/β-L-fucopyranosyl)-trichloroacetimidate from L-fucose was developed by introducing the thiophenyl group at the anomeric center and the benzylidene functional group to protect the 3 an
Glycosylation with trichloroacetimidates in ionic liquids: Influence of the reaction medium on the stereochemical outcome
Rencurosi, Anna,Lay, Luigi,Russo, Giovanni,Caneva, Enrico,Poletti, Laura
, p. 7765 - 7768 (2007/10/03)
The glycosylation with trichloroacetimidates derived from different glycopyranoses bearing a nonparticipating group at C-2 was explored in different ionic liquids as solvents. The stereoselectivity of the reaction was significantly affected by the reactio
