203862-58-2

Upstream product

• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 13035-12-6 3,4,6-tri-O-acetyl-1,2-dideoxy-D-glucopyranose 
• 2873-29-2 D-glucal triacetate 
• 3971-47-9 (3S,4R)-dihydroxy-(2R)-(hydroxymethyl)tetrahydropyran 

Downstream Products

• 1443743-53-0 C₂₇H₄₀O₄Si 
• 1443743-47-2 C₂₆H₃₈O₅Si 
• 1443743-55-2 C₄₄H₇₅NO₇Si₂ 
• 1443743-59-6 C₄₅H₇₇O₉PSi₂ 
• 1443743-60-9 C₃₉H₆₃O₉PSi 
• 1443743-45-0 C₃₉H₆₁O₉PSi 
• 1443743-51-8 C₂₁H₂₄O₅ 
• 1443743-52-9 C₂₁H₂₅IO₄ 
• 152569-25-0 1,5-anhydro-2,4-dideoxy-6-O-p-methoxybenzyl-3-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-D-threo-hexitol 

Relevant academic research and scientific papers

Approach to the tricyclic core of the tigliane-daphnane diterpenes. Concerning the utility of transannular aldol additions

Two transannular (TA) aldol reactions were used to assemble the tricyclic carbon skeleton found in the tigliane and daphnane classes of diterpene natural products.

Chiral compounds, and their use as chiral dopants for the preparation of cholesteric liquid-crystalline compositions

The use of compounds of the general formula I in which the substituents are as defined in the description, as chiral dopants for nematic or cholesteric liquid crystals for the generation of layers which reflect in color in the UV or IR region or for the preparation of pigments having a liquid-crystalline cholesteric order.

Inhibitors of endo-α-mannosidase. Part I. Derivatives of 3-O-(α-D-glucopyranosyl)-D-mannopyranose

Golgi membrane endo-α-D-mannosidase releases the disaccharide αDGlc(1 → 3)DMan (34) from the GlcMan9GlcNAc2 oligosaccharide of immature N-linked glycoproteins. To convert the hydrolysis product 34 into a potent inhibitor of the enzym