299174-91-7

Upstream product

• 108-98-5 thiophenol 
• 299174-88-2 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-1,2-O-(1-methoxyethylidene)-α-D-glucopyranose 
• 158198-56-2 phenyl 2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 299174-97-3 phenyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-O-succinyl-1-thio-β-D-glucopyranoside 
• 299174-94-0 phenyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

Chemoselective activation of ethyl: Vs. phenyl thioglycosides: One-pot synthesis of oligosaccharides

Ethyl and phenyl thioglycosides are the two most common types of thioglycoside donors in carbohydrate chemistry. However, the chemoselective activation of ethyl vs. phenyl thioglycosides is very rare in the literature. In this work, ethyl thioglycosides c

Prearranged glycosides, part 10.1 Intramolecular glycosylation with cellobiosyl, lactosyl, and maltosyl donors

Acetyl protected 1,2-O-(1-methoxyethylidene)-disaccharides 1 of maltose, cellobiose, and lactose, respectively were converted via the corresponding benzyl protected couterparts 2, the benzyl protected phenyl 2-O-acetyl- 3 and 2-O-unprotected 1-thio-glycos