114412-95-2

Upstream product

• 100-51-6 benzyl alcohol 
• 34819-86-8 3,4-di-O-acetyl-6-deoxy-L-glucal 
• 114412-85-0 4-O-Acetyl-2,3,6-trideoxy-L-erythro-hex-2-enopyranose 

Downstream Products

• 114413-04-6 benzyl α-L-acosaminide 
• 890122-90-4 (2S,3R,4S,6R)-(6-benzyloxy-3-methoxy-2-methyltetrahydropyran-4-yl)methylcarbamic acid tert-butyl ester 
• 890122-89-1 (2S,3R,4S,6R)-(6-benzyloxy-3-methoxy-2-methyltetrahydropyran-4-yl)carbamic acid tert-butyl ester 
• 890122-88-0 (2S,3R,4S,6R)-4-azido-6-benzyloxy-3-methoxy-2-methyltetrahydropyran 
• 890123-65-6 (2S,3R,4S,6R)-6-Benzyloxy-3-methoxy-2-methyl-tetrahydro-pyran-4-ylamine 
• 114413-02-4 benzyl 3-azido-2,3,6-trideoxy-α-L-arabino-hexopyranoside 

Relevant academic research and scientific papers

Facile synthesis of C-aryl glycals from sugar-derived lactones

A general entry to C(1) aryl-substituted glycals from the corresponding sugar lactones is described. This approach features one-pot access to aryl glycals. A variety of aryllithium reagents can be used and the method is compatible with various 2-deoxysuga

Addition of Hydrazoique Acid to Pseudoglycals Stereoselective Synthesis of L-Acosamine and L-Daunosamine

Methyl and benzyl glycosides and glycal of L-acosamine (3-amino-2,3,6 trideoxy-L-arabino-hexose) have been stereoselectively prepared via 1,4-addition of hydrazoic acid to L-erythro-hex-2-enopyranose as a key step.Inversion of the C-4 configuration of met

Stereocontrolled Route to 3-Amino-2,3,6-trideoxy-hexopyranoses. K-10 Montmorillonite as a Glycosidation Reagent for Acosaminide Synthesis

A stereoselective synthesis of methyl .(or benzyl) 3-azido-2,3,6-trideoxy-α-L-arabino-hexopyranoside from di-O-acetyl-L-rhamnal is reported; it proceeds via addition of hydrazoic acid to a hex-2-enopyranose, followed by acetylation and glycosidation with