2405-69-8

Upstream product

• 100-44-7 benzyl chloride 
• 87-99-0 XYLITOL 
• 488-81-3 Adonitol 
• 2159-34-4 1,5-Di-O-trityl-2,3,4-tri-O-benzyladonitol 
• 18039-26-4 2,3,4-tri-O-benzyloxy-L-arabinopyranose 
• 96871-07-7 1,5-Di-O-trityl-L-arabinitol 
• 7643-75-6 L-(-)-arabitol 
• 96871-07-7 1,5-di-O-tritylxylitol 

Downstream Products

• 96236-35-0 2,3,4-tri-O-benzyl-D-lyxose diethyl dithioacetal 
• 138481-64-8 Acetic acid (2R,3S,4S)-2,3,4-tris-benzyloxy-5-oxo-pentyl ester 
• 138481-57-9 Acetic acid (2R,3R,4R)-2,3,4-tris-benzyloxy-5-hydroxy-pentyl ester 
• 138481-60-4 Acetic acid (2R,4R)-5-acetoxy-2,3,4-tris-benzyloxy-pentyl ester 
• 2159-31-1 1,5-Di-O-toluene-p-sulfonyl-2,3,4-tri-O-benzyl-D-arabinitol 
• 138481-57-9 (2S,3R,4R)-1-O-Acetyl-2,3,4-tri-O-benzyladonitol 
• 138481-60-4 1,5-Di-O-acetyl-2,3,4-tri-O-benzyladonitol 
• 158931-72-7 N-Pentyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-imino-L-arabinitol 
• 158931-71-6 N-Butyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-imino-L-arabinitol 
• 158931-70-5 N-Propyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-imino-L-arabinitol 

Relevant academic research and scientific papers

One-pot cascade synthesis of azabicycles via the nitro-Mannich reaction and N -alkylation

A one-pot, metal-free process for the synthesis of azabicycles is developed. The key transformations involved a cascade of double intramolecular cyclizations via the nitro-Mannich reaction and N-alkylation, providing various ring systems of azabicycles in

Versatile sugar derivatives for the synthesis of potential degradable hydrophilic-hydrophobic polyurethanes and polyureas

Biodegradable polymers obtained from renewable natural sources are currently receiving increasing attention because they are an alternative to the traditional petroleum-based plastics. In the present communication we describe the synthesis of the diol mon

Nanomolar versus millimolar inhibition by xylobiose-derived azasugars: Significant differences between two structurally distinct xylanases

The synthesis of xylobiose-derived nitrogen-containing inhibitors of xylanase is described starting with accessible precursors through efficient synthetic schemes. Four disaccharides were identified as powerful competitive inhibitors of the retaining fami

Synthesis of cyclitols fused with a furoxan ring from alditols by intramolecular nitrile oxide dimerization

The synthesis of cyclitols fused with a furoxan ring has been achieved by conversion of an alditol to a bis-(aldoxime) and further oxidation of the oxime groups with N-chlorosuccinimide to nitrile oxides, which spontaneously dimerize intramolecularly to form a furoxan ring.

HYDROXYLATED PIPERIDINES: SYNTHESIS OF 1,5-ALKYLIMINO-1,5-DIDEOXY DERIVATIVES OF XYLITOL, D- AND L-ARABINITOL, AND RIBITOL

Direct routes are reported for the synthesis of N-propyl, N-butyl and N-pentyl-1,5-dideoxy-1,5-iminoxylitol (7a,b,c), the analogous derivatives (8a,b,c, and 9a,b,c) of 1,5-dideoxy-1,5-imino-D- and -L-arabinitol, and of N-propyl-1,5-dideoxy-1,5-iminoribito

A Route to Several Stereoisomers of Castanospermine

The following three stereoisomers of castanospermine have been prepared: (1R,6R,7R,8S,8aR)-1,6,7,8-tetrahydroxyindolizidine (1), (1R,6S,7S,8S,8aR)-1,6,7,8-tetrahydroxyindolizidine (2), and (1R,6R,7S,8S,8aR)-1,6,7,8-tetrahydroxyindolizidine (3).Each of the