121388-68-9

Upstream product

• 2131-61-5 p-nitrophenyl isothiocyanate 
• 13992-25-1 1-azido-1-deoxy-β-D-glucopyranoside tetraacetate 
• 6919-96-6 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 100-01-6 4-nitro-aniline 
• 14152-97-7 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate 

Downstream Products

• 121388-76-9 Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{2-[(Z)-4-nitro-phenylimino]-4-oxo-thiazolidin-3-yl}-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Preparation of glycosyl thiourea derivatives from glycosyl azides using sulfamic acid and sodium iodide in one-pot

Novel one-pot reaction conditions have been developed for the preparation of glycosyl thiourea derivatives directly from glycosyl azides mediated by a combination of sulfamic acid and sodium iodide. The reaction conditions were clean, non-toxic and the products were isolated in good to excellent yield.

Synthesis, Antimicrobial and Antifungal Activities of Some 2-Arylimino-4-tetra-O-acetyl-&β-D-glucopyranosyl-4-thiazolidinones

The title compounds (3) have been prepared by the condensation of 1-aryl-3-tetra-O-acetylglucopyranosylthiocarbamide (2) with monochloroacetic acid in the presence of anhydrous sodium acetate.The structure of the compounds have been established on the bas