71204-39-2Relevant academic research and scientific papers
SYNTHESIS OF L-NOGALOSE AND ITS ENANTIOMER
Hong, Namgi,Funabashi, Masuo,Yoshimura, Juji
, p. 21 - 28 (1981)
L-Nogalose (6-deoxy-3-C-methyl-2,3,4-tri-O-methyl-L-mannopyranose) and its enantiomer were synthesized via (a) introduction of the C-methyl branch by successive epoxidation and reduction of methyl 3,6-dideoxy-2,4-di-O-methyl-3-C-methylene-α-L-arabino-hexopyranoside, and (b) deoxygenation at C-6 of methyl 4,6-O-benzylidene-3-C-methyl-2-O-methyl-α-D-mannopyranoside, and O-methylation of the product.
