107079-29-8

Upstream product

• 98-88-4 benzoyl chloride 
• 80483-21-2 1,5-Anhydro-2,6-didesoxy-L-ribo-hex-1-enit 
• 115888-74-9 3,4-di-O-acetyl-L-rhamnal 
• 106988-66-3 3,4-Di-O-benzoyl-2,6-didesoxy-ξ-L-ribo-hexopyranose 

Downstream Products

• 106988-75-4 1,5-Anhydro-2,6-didesoxy-3-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 106988-76-5 1,5-Anhydro-2,6-didesoxy-4-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 106988-77-6 1,5-Anhydro-4-O-benzoyl-2,6-didesoxy-3-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 106988-78-7 1,5-Anhydro-3-O-benzoyl-2,6-didesoxy-4-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 106988-79-8 1,5-Anhydro-3,4-di-O-benzyl-2,6-didesoxy-L-ribo-hex-1-enit 

Relevant academic research and scientific papers

A facile route to steroidal 6-deoxy-α-L-allopyranosides

The synthesis of a steroidal 6-deoxy-α-L-allopyranoside from cholestanol and rhamnose is described. The crucial steps in the reaction sequence comprised the transformation of a pseudoglycal into the more steric hindered 2,3-cisdiol via an intermediate bro

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.