Structural elucidation of the cyclic products formed by the reaction of 2,3--isopropylidene derivatives of -aldose with allylsilanes, vinyl ethers, or vinyl sulfides in the presence of boron trifluoride etherate
Structural elucidation of the cyclic products formed by the reaction of 2,3--isopropylidene derivatives of -aldose with allylsilanes, vinyl ethers, or vinyl sulfides in the presence of boron trifluoride etherate
Phenyl 3-azido- and 3-fluoro-2, 3-dideoxy-1-thio-alpha-D-erythro-pentofuranosides and their 2-C-substituted derivatives, promising precursors of potent antiviral nucleosides, have been synthesized from L-arabinose.
SUGIMURA, HIDEYUKI, NOGUTI KEHNKYUDZE DZIXO,(1990) N3, S. 13-16