111407-92-2

Upstream product

• 99838-51-4 (E)-(1R,2S)-2-Benzyloxy-1-((2R,3S)-3-methyl-oxiranyl)-pent-3-en-1-ol 
• 99944-94-2 2,3-anhydro-5-O-benzyl-1,6,7,8-tetradeoxy-L-galacto-oct-6-enitol 
• 4486-59-3 dl-2,6-octadiene-4,5-diolhexanediene-3,4-diol 
• 100-39-0 benzyl bromide 
• 99838-50-3 D,L-threo-5-O-benzyl-2,6-octadien-4,5-diol 
• 111407-93-3 2,3-anhydro-5-O-benzyl-1,6,7,8-tetradeoxy-L-altro-oct-6-enitol 
• 102517-71-5 meso-2,6-octadiene-4,5-diolhexanediene-3,4-diol 
• 99838-50-3 D,L-erythro-5-O-benzyl-2,6-octadien-4,5-diol 

Downstream Products

• 99838-53-6 2-O-Benzoyl-4,6-didesoxy-D-xylo-hexose 
• 99838-53-6 2-O-benzyl-4,6-dideoxy-L-lyxo-hexose 
• 111304-14-4 benzyl 2-O-benzyl-4,6-dideoxy-β-L-lyxo-hexopyranoside 
• 33302-99-7 L-lyxo-4,6-dideoxy-hexose 
• 29325-32-4 D-xylo-4,6-dideoxy-hexose 
• 111304-09-7 (3R,4S,6R)-2,3-Bis-benzyloxy-4-methoxy-6-methyl-tetrahydro-pyran 
• 111304-07-5 (3R,4S,6R)-2,3-Bis-benzyloxy-6-methyl-tetrahydro-pyran-4-ol 

Relevant academic research and scientific papers

SYNTHESIS OF 4,6-DIDEOXY-D- AND -L-HEXOSES FROM RACEMIC AND meso-DIPROPENYLGLYCOL

Rac- and meso-divinylglycols offer, via site-selective epoxidation, a versatile strategy for the synthesis of optically pure sugars.This is exemplified in this paper by the synthesis of 4,6-dideoxyhexoses.Starting from mono-O-benzyl di-(1-propenyl)glycol,