891785-94-7

Upstream product

• 130405-48-0 (2R,3S,6S)-2-(hydroxymethyl)-6-phenyl-3,6-dihydro-2H-pyran-3-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 201232-86-2 (4,6-di-O-tert-butyldimethylsilyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl)benzene 

Downstream Products

• 1233959-33-5 tert-butyl(((2R,3S,6S)-3-(3-methoxybenzyloxy)-6-phenyl-3,6-dihydro-2H-pyran-2-yl)methoxy)dimethylsilane 

Relevant academic research and scientific papers

Skeletal diversity via cationic rearrangements of substituted dihydropyrans

(Figure Presented) Substituted dihydropyrans, easily accessed from a commercially available glycal, undergo acid-catalyzed rearrangement to provide highly functionalized isochroman and dioxabicyclooctane scaffolds.

Epoxidation and bis-hydroxylation of C-phenyl-Δ2,3- glycopyranosides

Epoxidation and cis-hydroxylation of C-phenyl-Δ2,3 -glycopyranosides have been carried out with a view to developing C-aryl glycoside synthesis. Epoxidation of (2,3-dideoxy-D-erythro-hex-2-enopyranosyl) benzene and (6-O-tert-butyldimethylsilyl-