4631-19-0

Upstream product

• 4627-39-8 1,3,4,6-tetra-O-acetyl-2-O-p-toluenesulfonyl-β-D-glucopyranose 
• 4581-93-5 1,3,4,6-tetra-O-acetyl-2-O-p-toluenesulfonyl-α-D-glucopyranose 
• 111408-49-2 1-chloro-2-O-tosyl-3,4,6-tri-O-acetyl-α-D-glucopyranose 
• 6167-32-4 1,6:3,4-dianhydro-2-O-tosyl-D-galactose 
• 3868-05-1 1,6-anhydro-2-O-(4-toluenesulfonyl)-β-D-glucopyranose 
• 128947-68-2 1,3,4-tri-O-acetyl-2,6-di-O-p-tolylsulfonyl-α-D-glucopyranose 
• 13036-15-2 1,3,4,6-tetra-O-acetyl-β-D-glucopyranose 
• 98-59-9 p-toluenesulfonyl chloride 
• 10035-10-6 hydrogen bromide 
• 64-19-7 acetic acid 
• 84207-46-5 3,4-di-O-acetyl-1,6-anhydro-2-O-p-toluenesulfonyl-β-D-glucopyranose 

Downstream Products

• 910887-20-6 methyl-[O³,O⁴,O⁶-triacetyl-O²-(toluene-4-sulfonyl)-β-D-glucopyranoside] 

Relevant academic research and scientific papers

PREPARATION OF 1,6:3,4-DIANHYDRO-β-D-ALTROPYRANOSE AS STARTING SUBSTANCE FOR THE SYNTHESIS OF 3-SUBSTITUTED D-MANNOSE DERIVATIVES

Acetolysis of 1,6:3,4-dianhydro-2-O-p-toluenesulfonyl-β-D-galactopyranose (I) gave 3,4-di-O-acetyl-1,6-anhydro-2-O-p-toluenesulfonyl-β-D-glucopyranose (II) which was converted with sodium methoxide to 1,6:3,4-dianhydro-β-D-altropyranose (X).The 1,6-anhydride bond in diacetate II was cleaved with acetic anhydride or hydrogen bromide in acetic acid under formation of a mixture of anomeric tetraacetates of 2-O-p-toluenesulfonyl-D-glucopyranose or the corresponding acetates of α-D-glucopyranosyl bromide XIII and its 6-bromo-6-deoxy derivative XIV.