328047-23-0

Upstream product

• 196703-95-4 1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-triisopropylsilyl-D-arabino-hex-1-enitol 
• 13154-24-0 triisopropylsilyl chloride 
• 2873-29-2 D-glucal triacetate 
• 137915-37-8 1,2-dideoxy-6-O-triisopropylsilyl-D-arabino-1-hexenopyranose 

Downstream Products

• 196703-97-6 thioethyl 3,4-di-O-benzyl-6-O-triisopropylsilyl-β-D-glucopyranoside 
• 328047-25-2 (2R,3S,4R,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-triisopropylsilanyloxymethyl-tetrahydro-pyran-3-ol 
• 328047-24-1 (2S,3S,4R,5R,6R)-2-Allyl-4,5-bis-benzyloxy-6-triisopropylsilanyloxymethyl-tetrahydro-pyran-3-ol 
• 196704-14-0 4-Methoxy-benzoic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-ethylsulfanyl-6-triisopropylsilanyloxymethyl-tetrahydro-pyran-3-yl ester 
• 196704-08-2 Benzoic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-ethylsulfanyl-6-triisopropylsilanyloxymethyl-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Concise synthesis of 3-O-(2-O-α-D-glucopyranosyl-6-O-acyl-α-D-glucopyranosyl)-1,2-di-O-acyl-sn-g lycerols

A versatile synthetic route to 3-O(2-O-α-D-glucopyranosyl-6-O-acyl-α-D-glucopyranosyl)-1,2-di-O-acyl-sn-gl ycerols, which should provide various acyl derivatives, has been developed. (C) 2000 Elsevier Science Ltd.

A mercury-catalyzed transetherification cyclization leading to fused cyclic polyethers

Dihydropyran 6 serves as a key intermediate in a route to fused cyclic polyethers. The dihydropyran was first converted to 2-hydroxy-1-γ-methoxyallyltetrahydropyrans, 10. Mercury trifluoroacetate-catalyzed transetherification cyclization generated new bic

Coupling of glycal derived thioethyl glycosyl donors with glycal acceptors. An advance in the scope of the glycal assembly

Glycals were converted into thioethyl glycosyl donors through 1,2-anhydrosugar intermediates. Various participating groups in the C-2 position were examined for formation of β-glucosyl, β-galactosyl, and α-mannosyl linkages. A number of disaccharides was