Chemistry Letters p. 1529 - 1530 (1984)
Update date:2022-07-30
Topics: Synthesis Nucleophile Trityl perchlorate Reaction Facile Synthesis Activation
Mukaiyama, Teruaki
Kobayashi, Shu
Shoda, Shin-ichiro
In the presence of a catalytic amount of trityl perchlorate, 1-o-acetyl ribose stereoselectively reacts with silylated nucleophiles, such as silyl enol ether, allylsilane, and trimethylsilyl cyanide, to give the corresponding α-C-ribofuranosides in excell
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