66854-07-7

Upstream product

• 112-53-8 1-dodecyl alcohol 
• 604-69-3 β-D-glucose pentaacetate 
• 4163-60-4 β-D-galactose peracetate 

Downstream Products

• 59122-55-3 n-dodecyl-b-D-glucopyranoside 
• 6801-92-9 n-dodecanyl β-D-galactopyranoside 
• 263247-08-1 dodecyl 3,4-O-isopropylidene-6-O-tert-butyldiphenylsilyl-β-D-galactopyranoside 
• 263247-10-5 dodecyl 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->2)-3,4-O-isopropylidene-β-D-galactopyranoside 
• 263247-09-2 dodecyl 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->2)-6-O-tert-butyldiphenylsilyl-3,4-O-isopropylidene-β-D-galactopyranoside 
• 1427214-08-1 dodecyl 4,6-O-benzylidene-β-D-galactopyrnoside 
• 1427214-18-3 dodecyl 4,6-O-benzylidene-2,3-[15-cr-5]triazadiamido-β-D-galactopyranoside 
• 1427214-16-1 dodecyl 4,6-O-benzylidene-2,3-[15-cr-5]thiadiamido-β-D-galactopyranoside 
• 1427214-14-9 dodecyl 4,6-O-benzylidene-2,3-bis-[2-(2-chloroacetamido)ethyl]-β-D-galactopyranoside 
• 1427214-12-7 dodecyl 4,6-O-benzylidene-2,3-bis-(2-aminoethyl)-β-D-galactopyranoside 
• 1427214-10-5 dodecyl 4,6-O-benzylidene-2,3-bis-O-[cyanomethyl]-β-D-galactopyranoside// 
• 504422-56-4 dodecyl 2-O-acetyl-3-O-benzyl-4,6-di-O-methanesulfonyl-5a-carba-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 504422-57-5 dodecyl 2,4,6-tri-O-acetyl-3-O-benzyl-5a-carba-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 504422-51-9 dodecyl 2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-5a-carba-α-D-mannopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

BF3 etherate-induced formation of C7-C 16-alkyl β-D-glucopyranosides

BF3 etherate-induced formation of C7-C 16-alkyl D-glucopyranosides is used as the key step in their synthesis from glucose and C7-C16-alkanols.

Synthesis of C7-C16-alkyl glycosides: Part III - Synthesis of alkyl D-galactopyranosides in the presence of tin(IV) chloride as a Lewis acid catalyst

The Lewis acid catalyzed glycosylation reaction of β-peracetylated sugar derivative (galactose) with fatty alkanols is used in a synthesis of C7-C16-alkyl galactopyranosides. The process occurs under the influence of tin(IV) chloride as a Lewis acid catalyst.

Synthesis of C7-C16-alkyl glycosides: Part I - Synthesis of alkyl D-glucopyranosides in the presence of tin (IV) chloride as a Lewis acid catalyst

The Lewis acid catalyzed glycosylation reaction of β-peracetylated sugar derivative (glucose) with fatty alkanols is used in a synthesis of C7-C16-alkyl glucopyranosides. The process occurs under the influence of tin (IV) chloride.