97693-91-9Relevant academic research and scientific papers
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
, 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-
