228115-90-0

Upstream product

• 52443-07-9 3,4,5,7-tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptonitrile 
• 140461-65-0 (2',3',4',6'-tetra-O-benzyl-β-D-galactopyranosyl)methyl alcohol 
• 140397-46-2 (2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)methanal 
• 228115-89-7 1,3-diphenyl-2-(2,3,4-tri-O-benzyl-6-O-triphenylmethyl-β-D-galactopyranosyl)-imidazolidine 
• 228115-88-6 1,3-diphenyl-2-(6-O-triphenylmethyl-β-D-galactopyranosyl)-imidazolidine 
• 71420-08-1 1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)imidazolidine 

Downstream Products

• 228115-91-1 Toluene-4-sulfonic acid (2R,3S,4R,5S,6S)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-ylmethyl ester 
• 228115-91-1 Toluene-4-sulfonic acid (2S,3S,4S,5S,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-ylmethyl ester 
• 228115-93-3 C₄₂H₄₄O₁₀S₂ 

Relevant academic research and scientific papers

Synthesis of β-C-Glycopyranosyl Aldehydes and 2,6-Anhydro-heptitols

A convenient route has been developed for the diastereoselective synthesis of β-C-glycopyranosyl aldehydes from d-glucose, d-mannose, and d-galactose. The key step in the synthesis of C-glycosyl aldehydes is the aryl driven reductive dehydration on 1-phen

Synthesis studies of structural analogues of tagetitoxin: 4-O-acetyl-3- amino-1,6-anhydro-3-deoxy-D-gulose 2-phosphate

Synthetic approaches to structural analogues of tagetitoxin (1) are described. The successful route to analogue 3 (X=O) has, as a key step, protection of the cis-vicinal amino alcohol moiety of compound 7 as an N- benzylated cyclic carbamate (9). X-Ray cr