175289-53-9Relevant academic research and scientific papers
Higher sucrose analogs: Homologation of a glucose unit of sucrose by two carbon atoms
Jarosz, Slawomir,Mach, Mateusz
, p. 1111 - 1122 (2007/10/03)
The primary hydroxyl groups (at C-6 and C-6′) in 2,3,4,3′4′-penta-O-benzyl-1′-O-methoxymethyl sucrose (2) can be reactively differentiated with tert-butyldiphenylsilyl chloride. Reaction of 2 with TBDPSC1 afforded only one monosilylated product protected
Selective reactions of the free hydroxyl groups of 2,3,4,3′,4′-penta-O-benzylsucrose
Jarosz, Slawomir
, p. 73 - 79 (2007/10/03)
Selective transformations of the free hydroxyl groups in 2,3,4,3′,4′-penta-O-benzylsucrose (1) were studied. Oxidation of 1 with the Swern reagent followed by reaction with Ph3P=CH-COOMe gave 2,3,4,3′,4′-penta-O-benzyl-1,6,6′-tris-(E)(C-carbome
