Gigg, Roy published the artcileUse of the allyl ether as a protecting group in a new synthesis of L-lyxose, Recommanded Product: (2R,3R,4S,5R,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol, the main research area is .
Crystalline 2,3,4-tri-O-benzyl-D-galactose was prepared from allyl 6-O-allyl- 2,3,4-tri-O-benzyl-α-D-galactopyranoside by isomerization of the allyl groups to prop-1-enyl groups and removal by dilute-acid hydrolysis. Reduction by NaBH4 gave crystalline 2,3,4-tri-O-benzyl-D- galactitol which was converted into 2,3,4-tri-O-benzyl-L-lyxose by oxidation with NaIO4. Catalytic hydrogenation gave L-lyxose.
Journal of the Chemical Society published new progress about Allyl group. 2595-07-5 belongs to class alcohols-buliding-blocks, name is (2R,3R,4S,5R,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol, and the molecular formula is C9H16O6, Recommanded Product: (2R,3R,4S,5R,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts