80245-08-5Relevant articles and documents
Rapid and efficient synthesis of α(1-2)mannobiosides
Reina, José J.,Di Maio, Antonio,Ramos-Soriano, Javier,Figueiredo, Rute C.,Rojo, Javier
, p. 2873 - 2882 (2016/03/12)
α(1,2)mannobiosides with different substituents at the reducing end have been synthesized by a common strategy using benzoyls as the permanent protecting groups and an acetyl as the orthogonal protecting group at position C2 of the glycosyl acceptor. The
REGIOSELECTIVE O-DEACYLATION OF FULLY ACYLATED GLYCOSIDES AND 1,2-O-ISOPORPYLIDENEALDOFURANOSE DERIVATIVES WITH HYDRAZINE HYDRATE
Ishido, Yoshiharu,Sakairi, Nobuo,Sekiya, Masao,Nakazaki, Nobuo
, p. 51 - 80 (2007/10/02)
On hydrazinolyis in 1:4 acetic acid-pyridine, and in pyridine, partisl O-deacylation of fully acylated methyl glycosides and some other glycosyl compounds ( 23 compounds ) was found to be induced, to give, in good yields, products bearing one free hydroxy