101024-17-3

Upstream product

• 101024-16-2 1,6-anhydro-4-O-benzyl-2,3-dideoxy-2,3-epimino-β-D-allopyranose 
• 122-04-3 4-nitro-benzoyl chloride 
• 101024-10-6 C₁₄H₁₆NO₄S₂^(1-)*Na⁽¹⁺⁾ 
• 101024-14-0 1,6-anhydro-4-O-benzyl-2-deoxy-2-isothiocyanato-3-O-p-toluenesulfonyl-β-D-glucopyranose 
• 101024-11-7 1,6-anhydro-4-O-benzyl-2-deoxy-2-isothiocyanato-β-D-glucopyranose 
• 50447-92-2 2-amino-1,6-anhydro-4-O-benzyl-2-deoxy-β-D-glucopyranose 

Relevant academic research and scientific papers

REACTION OF 1,6-ANHYDRO-4-O-BENZYL-2-DEOXY-2-ISOTHIOCYANATO-β-D-GLUCOYRANOSE; PREPARATION OF 2-AMINO-1,6-ANHYDRO-2,3-DIDEOXY-β-D-ribo-HEXOPYRANOSE

1,6-Anhydro-4-O-benzyl-2-deoxy-2-isothiocyanato-β-D-glucopyranose (IV), prepared from 2-amino-1,6-anhydro-4-O-benzyl-2-deoxy-β-D-glucopyranose (I) by reaction with carbon disulfide followed by oxidation with iodine, was converted into the 3-O-p-toluenesulfonate VII.This was cyclized to give either the 2,3-epimino derivative X or the thiazoline XII. 2-Acetamido-3-S-acetyl-1,6-anhydro-4-O-benzyl-2-deoxy-3-thio-β-D-glucopyranose (XVI), obtained from compound XII, was desulfurized with Raney nickel to afford 2-acetamido-1,6-anhydro-2,3-dideoxy-β-D-ribo-hexopyranose (XVII).The isothiocyanato group was not affected upon acetylation of compound IV and acetolysis of the 1,6-anhydride bond with acetic anhydride and trifluoroacetic acid.