128461-99-4Relevant academic research and scientific papers
Synthetic Study toward Vineomycins. Synthesis of C-Aryl Glycoside Sector via Cp2HfCl2-AgClO4-Promoted Tactics
Matsumoto, Takashi,Katsuki, Miyoko,Jona, Hideki,Suzuki, Keisuke
, p. 6185 - 6188 (1989)
Regio- and stereo-controlled formation of C-aryl β-D-olivoside linkage is achieved by the reaction of naphthol or anthrol derivatives with D-olivosyl fluoride.The reaction is efficiently promoted by Cp2HfCl2-AgClO4 and the bond formation occurs selectivit
