259871-12-0Relevant articles and documents
Prearranged glycosides. Part 8. Intramolecular α-galactosylation via succinoyl tethered glycosides
Ziegler, Thomas,Dettmann, Ralf,Ariffadhillah,Zettl, Uwe
, p. 1079 - 1095 (1999)
Benzyl protected phenyl 1-thio-galactopyranoside donors which were tethered by a succinoyl linker at their positions 2 and 6, respectively, to position 3 of a blocked benzyl glucopyranoside acceptor with a 4-OH group solely afforded the corresponding α-(1→4)-linked disaccharides upon intramolecular glycosylation. 4,6-Siloxane protected mannosides react with rearrangement of the siloxane group under similar conditions.