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Usage

Uses

Used in Fragrance Industry:
3,5-diacetoxy-2-acetoxymethyl-6-phenethyl-tetrahydro-pyran-4-yl ester is used as a fragrance ingredient for its pleasant aroma.
Used in Flavoring Industry:
3,5-diacetoxy-2-acetoxymethyl-6-phenethyl-tetrahydro-pyran-4-yl ester is used as a flavoring agent for its taste-enhancing properties.
Used in Pharmaceutical Industry:
3,5-diacetoxy-2-acetoxymethyl-6-phenethyl-tetrahydro-pyran-4-yl ester is used as a pharmaceutical compound for its potential physiological effects. Further research and analysis would be needed to determine its specific applications and properties in this industry.

Upstream product

• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 100-42-5 styrene 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 74352-41-3 2-Pyridyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-galactopyranoside 
• 108-24-7 acetic anhydride 
• 96689-92-8 α-1-deoxy-1-(C-1'-phenethyl)-2,3,4,6-tetra-O-acetyl-D-glucopyranose 
• 85422-87-3 2-(2,3,4,6-Tetra-O-benzyl-α,β-D-glucopyranosyl)acetophenon 

Relevant academic research and scientific papers

Sn-free Ni-catalyzed reductive coupling of glycosyl bromides with activated alkenes

A mild, stereoselective method for the Ni-catalyzed synthesis of α-C-alkylglycosides is reported. This approach entails the reductive coupling of glycosyl bromides with activated alkenes at room temperature, with low alkene loading as an important feature. Diastereoselective coupling with 2-substituted acrylate derivatives was made possible through the use of 2,4-dimethyl-3-pentanol as a proton source.

O-Glycosyl Imidates, 19. - Reactions of Glycosyl Trichloroacetimidates with Silylated C-Nucleophiles

Reaction of O-benzyl-protected α-glycopyranosyl trichloroacetimidates 1 and the xylo analogues 7 with silyl enol ethers or allyltrimethylsilane as C-nucleophiles yields with zink chloride as catalyst mainly or exclusively α-C-glycosides (5a-α to 5h-α, 8b,