70798-30-0Relevant articles and documents
Regioselective ring opening of exo- and endo-3,4-benzylidene acetals of arabinopyranoside derivatives with Lewis acids and reducing agents
Rujirawanich, Janjira,Kongkathip, Boonsong,Kongkathip, Ngampong
experimental part, p. 927 - 932 (2011/06/20)
Dioxolane type 3,4-benzylidene acetals of benzyl β-l-arabinose either as a mixture or pure exo- and endo-isomers cleavaged with BF3· OEt2/Et3SiH in dichloromethane or acetonitrile regioselectively, provided the 4-O-benzyl-
One-pot acetalation-acetylation of sugar derivatives employing perchloric acid immobilised on silica
Mukhopadhyay, Balaram,Russell, David A.,Field, Robert A.
, p. 1075 - 1080 (2007/10/03)
Perchloric acid immobilised on silica gel has been used as an efficient promoter for per-O-acetylation, and acetalation and subsequent O-acetylation of glycosides and thioglycosides in one-pot using stoichiometric reagents.