106988-77-6

Upstream product

• 98-88-4 benzoyl chloride 
• 106988-75-4 1,5-Anhydro-2,6-didesoxy-3-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 68673-58-5 (2S,3S)-3-hydroxy-2-methyl-2H-pyran-4(3H)-one 
• 80483-21-2 1,5-Anhydro-2,6-didesoxy-L-ribo-hex-1-enit 
• 107079-29-8 1,5-Anhydro-3,4-di-O-benzoyl-2,6-didesoxy-L-ribo-hex-1-enit 
• 106988-66-3 3,4-Di-O-benzoyl-2,6-didesoxy-ξ-L-ribo-hexopyranose 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 128848-16-8 benzyl 3-O-(4-O-benzoyl-2,6-dideoxy-2-iodo-α-L-altropyranosyl)-4-O-benzyl-2,6-dideoxy-α-L-ribo-hexopyranoside 
• 128848-15-7 benzyl 3-O-<3-O-(p-methoxybenzyl-)2,6-dideoxy-α-ribo-hexopyranosyl>-4-O-benzyl-2,6-dideoxy-α-ribo-hexopyranoside 
• 128848-17-9 benzyl 4-O-benzoyl-2,6-dideoxy-2-iodo-3-O-(p-methoxybenzyl)-α-L-altropyranoside 
• 128848-14-6 benzyl 3-O-<4-O-benzoyl-2,6-dideoxy-2-iodo-3-O-(p-methoxybenzyl)-α-L-altropyranosyl>-4-O-benzyl-2,6-dideoxy-α-L-ribo-hexopyranoside 

Relevant academic research and scientific papers

Syntheses of Selectively Alkylated Enol Ethers in the L-ribo Series

The reduction of enulose 1a predominantly leads to L-digitoxal (3a), although this method presents a sluggish reaction with moderate yields.In contrast, the preparation from L-digitoxose (4a) in a three-step one-pot procedure represents an advantageous approach.Regioselective 3- or 4-O-alkylations are achieved by phase-transfer catalysis method or via stannylidene intermediates to give monosaccharide precursors of the L-ribo series valuable for further interglycosidic linking.