40592-74-3

Upstream product

• 76951-66-1 1,2:3,4-di-O-isopropylidene-6-O-trityl-α-D-galactopyranose 
• 75557-23-2 3,4,6-tri-O-acetyl-1,2-O-(1-p-tolylthioethylidene)-α-D-glucopyranose 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 13992-16-0 (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 32934-24-0 ethyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

1,6-Epithio- and 1,6-Episeleno-β-D-glucopyranose: Useful Adjuncts in the Synthesis of 6-Deoxy-β-D-glucopyranosides

Derivatives of 1,6-dideoxy-1,6-epithio- and 1,6-dideoxy-1,6-episeleno-β-D-glucopyranose have been shown to be effective glycosyl donors toward carbohydrate alcohols under the agency of N-iodosuccinimide/trifluoromethanesulfonic acid. Reduction of the inte

STANNOUS TRIFLATE MEDIATED GLYCOSIDATIONS. A STEREOSELECTIVE SYNTHESIS OF β-D-GLUCOSIDES.

Various 1,2 trans, β-D-linked disaccharides with glucose as non-reducing unit have been prepared with complete stereoselectivity from acetobromoglucose and suitably protected sugar derivatives using stannous triflate as promoter.