224964-50-5

Upstream product

• 7474-05-7 (R)-2-chloropropionic acid 
• 74984-84-2 prop-2-en-1-yl 2-(acetylamino)-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 1171121-75-7 C₁₉H₂₅NO₇ 
• 108-24-7 acetic anhydride 

Downstream Products

• 224964-56-1 2-{2-[2-(7-acetylamino-6-allyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-propionylamino]-propionylamino}-4-{5-acetylamino-1-[1-(1-benzyloxycarbonyl-ethylcarbamoyl)-ethylcarbamoyl]-pentylcarbamoyl}-butyric acid benzyl ester 

Relevant academic research and scientific papers

Widely applicable deprotection method of 2,2,2-trichloroethoxycarbonyl (Troc) group using tetrabutylammonium fluoride

The N-Troc (2,2,2-trichloroethoxycarbonyl) groups in glucosamine and muramic acid derivatives were removed by treatment with tetrabutylammonium fluoride (TBAF) under mild conditions. The use of Troc protection for the amino group in aminosugars such as gl

Synthesis of extended bacterial cell-wall precursor analogues for ligand binding studies with glycopeptide antibiotics

The synthesis of bacterial cell-wall precursor analogues, which resemble the naturally occurring precursor (lipid II) more closely than those hitherto used in NMR binding studies with glycopeptide antibiotics, is reported.