167874-35-3

Upstream product

• 14686-89-6 (1,2:5,6)-di-O-isopropylidene-D-gulose 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 
• 22331-21-1 1,2:5,6-di-O-isopropylidene-3-O-benzyl-α-D-allofuranose 
• 182418-02-6 (2R,3R,4R,5R,6R)-4-Benzyloxy-2-hydroxymethyl-6-isobutoxy-tetrahydro-pyran-3,5-diol 
• 182418-00-4 C₃₈H₃₈O₉ 
• 182698-06-2 C₄₁H₃₄O₁₀ 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 108-24-7 acetic anhydride 
• 182417-83-0 (2R,4aR,6R,7R,8S,8aR)-8-Benzyloxy-6-isobutoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 

Downstream Products

• 182418-17-3 ((2R,3R,4R,5R,6R)-4-Benzyloxy-6-isobutoxy-5-isopropoxy-2-trityloxymethyl-tetrahydro-pyran-3-yloxy)-acetic acid tert-butyl ester 
• 182418-08-2 (2R,3R,4R,5R,6R)-4-Benzyloxy-2-hydroxymethyl-6-isobutoxy-5-isopropoxy-tetrahydro-pyran-3-ol 
• 182417-85-2 ((2R,3R,4R,5R,6R)-4-Benzyloxy-2-hydroxymethyl-6-isobutoxy-5-isopropoxy-tetrahydro-pyran-3-yloxy)-acetic acid tert-butyl ester 
• 182418-23-1 [(2R,3R,4R,5R,6R)-4-Benzyloxy-6-isobutoxy-5-isopropoxy-2-(naphthalen-2-yloxymethyl)-tetrahydro-pyran-3-yloxy]-acetic acid tert-butyl ester 
• 182418-12-8 (2R,3R,4R,5R,6R)-4-Benzyloxy-6-isobutoxy-5-isopropoxy-2-trityloxymethyl-tetrahydro-pyran-3-ol 
• 182418-27-5 ((2R,3R,4R,5R,6R)-4-Benzyloxy-6-isobutoxy-5-isopropoxy-2-trifluoromethanesulfonyloxymethyl-tetrahydro-pyran-3-yloxy)-acetic acid tert-butyl ester 
• 167874-42-2 (2R,4aR,6R,7R,8R,8aR)-8-Benzyloxy-6-isobutoxy-7-isopropoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 

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