35808-11-8

Upstream product

• 19312-53-9 2-<3-(4-chlorophenyl)ureido>-2-deoxy-D-glucopyranose 
• 149117-59-9 (4R,5R)-4-(D-arabino-tetritol-1-yl)-1-(4-chlorophenyl)-5-hydroxyimidazolidin-2-one 
• 104-12-1 p-chlorphenylisocyanate 
• 149117-40-8 2-<3-(4-chlorophenylureido)>-2-deoxy-α-D-glucopyranose 
• 129784-21-0 1,3,4,6-Tetra-O-acetyl-2-<3-(4-chlorophenyl)ureido>-2-deoxy-α-D-glucopyranose 
• 10034-19-2 1,3,4,6-tetra-O-acetyl-2-amino-2-deoxy-α-D-glucopyranose hydrochloride 

Relevant academic research and scientific papers

THE REACTION OF 2-AMINO-2-DEOXYHEXOPYRANOSES WITH ISOCYANATES. SYNTHESIS OF UREAS AND THEIR TRANSFORMATION INTO HETEROCYCLIC DERIVATIVES.

The reactions of 2-amino-2-deoxyglycopyranoses with aryl isocyanates have been investigated in detail and ureas and heterocyclic derivatives are obtained.The mechanism of formation of glycofuranoimidazolidin-2-ones 62 has now become visible, while

Synthesis of glycofuranoimidazolidin-2-ones

Several 2-(3-arylureido)-2-deoxyglycopyranoses (13-16) have been converted into the corresponding 1-aryl-(1,2-dideoxyglycofurano)imidazolidin-2-ones (17-20) by acid-catalyzed cyclization.Acetylation of these compounds gave 1-aryl-(per-O-acetyl-1,2-