725740-19-2

Upstream product

• 884525-59-1 Acetic acid (2R,3R,4R,5R,6R)-3-acetoxy-2-azidomethyl-5-benzyloxycarbonylamino-6-phenoxy-tetrahydro-pyran-4-yl ester 
• 122210-05-3 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-glucopyranose 
• 725740-18-1 Acetic acid (2S,3S,4R,5R,6R)-3-acetoxy-5-benzyloxycarbonylamino-2-bromomethyl-6-phenoxy-tetrahydro-pyran-4-yl ester 
• 108-95-2 phenol 
• 501-53-1 benzyl chloroformate 
• 725740-17-0 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-benzyloxycarbonylamino-6-phenoxy-tetrahydro-pyran-4-yl ester 
• 669763-26-2 (2R,3S,4R,5R,6R)-2-(acetoxymethyl)-6-phenoxy-5-((2,2,2-trichloroethoxy)carbonylamino)tetrahydro-2H-pyran-3,4-diyl diacetate 
• 884525-57-9 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-5-benzyloxycarbonylamino-6-phenoxy-2-(toluene-4-sulfonyloxymethyl)-tetrahydro-pyran-4-yl ester 

Downstream Products

• 884525-76-2 1-((2R,3S,4R,5R,6R)-5-Amino-3,4-dihydroxy-6-phenoxy-tetrahydro-pyran-2-ylmethyl)-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-hydroxymethyl-5-((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yl]-urea 
• 884525-74-0 (6-{3-[3,4-dihydroxy-6-hydroxymethyl-5-(3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yl]-ureidomethyl}-4,5-dihydroxy-2-phenoxy-tetrahydro-pyran-3-yl)-carbamic acid benzyl ester 
• 884525-72-8 ((2R,3R,4R,5S,6R)-6-Aminomethyl-4,5-dihydroxy-2-phenoxy-tetrahydro-pyran-3-yl)-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of urea-tethered neoglycoconjugates and pseudooligosaccharides in water

A novel approach to the synthesis of urea glycosides in aqueous media has been explored. Steyermark's glucopyranosyl oxazolidinone was found to be a good synthon for anchoring glucosyl moieties onto amines and thiols. The present method was successfully a

Urea glycoside synthesis in water

A novel approach to the synthesis of urea glycosides in aqueous media has been developed. Reaction of Steyermark's glucosyl carbamate 1 with amines was carried out in water to afford urea glucosides in good yields. This method was successfully applied to