182418-24-2

Upstream product

• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 182698-05-1 C₄₁H₃₄O₁₀ 
• 182417-99-8 C₃₈H₃₈O₉ 
• 182418-13-9 (2R,3R,4S,5R,6R)-4-Benzyloxy-5,6-diisobutoxy-2-trityloxymethyl-tetrahydro-pyran-3-ol 
• 182418-03-7 (2R,4aR,6R,7R,8S,8aR)-8-Benzyloxy-6-isobutoxy-7-(2-methyl-allyloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 182417-89-6 (2R,4aR,6R,7R,8S,8aR)-8-Benzyloxy-6,7-diisobutoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 182417-82-9 (2R,4aR,6R,7R,8R,8aR)-8-Benzyloxy-6-isobutoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 182418-09-3 (2R,3R,4S,5R,6R)-4-Benzyloxy-2-hydroxymethyl-5,6-diisobutoxy-tetrahydro-pyran-3-ol 
• 182418-01-5 (2R,3R,4S,5R,6R)-4-Benzyloxy-2-hydroxymethyl-6-isobutoxy-tetrahydro-pyran-3,5-diol 
• 182418-19-5 ((2R,3R,4S,5R,6R)-4-Benzyloxy-5,6-diisobutoxy-2-trityloxymethyl-tetrahydro-pyran-3-yloxy)-acetic acid tert-butyl ester 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 100-39-0 benzyl bromide 

Relevant academic research and scientific papers

Synthesis of potential peptidomimetics based on highly substituted glucose and allose scaffolds

A series of eight potential peptidomimetics has been synthesised based on the use of gluco- and allo- carbohydrate derivatives as scaffolds to support appropriate side-chains which mimic the D- and L-aminoacid residues of the cyclic peptide endothelin ant