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Y-Lactone reduction

Hydrogenation of the double bond in 58 afforded the diol 64, which was ozonized to 4,5-dihydroxy-hexanoic acid, isolated in the form of a y-lactone. Reduction of the lactone grouping to the lactol stage afforded 2,3,6-trideoxy-L-eO o-hexopyranose (65, R = H, L-amicetose). [Pg.158]

See other pages where Y-Lactone reduction is mentioned: [Pg.462] [Pg.462]

See also in sourсe #XX -- [ Pg.19 , Pg.470 ]

See also in sourсe #XX -- [ Pg.19 , Pg.470 ]

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Lactones reduction

Lactones y-lactone

Y-lactone