184653-30-3

Upstream product

• 67-56-1 methanol 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 119068-33-6 phenyl 3,4,6-tri-O-benzyl-2-deoxy-1-sulphonyl-αβ-D-arabino-pyranoside 
• 127994-68-7 methyl onate 
• 120852-00-8 methyl 4,5,7-tri-O-benzyl-2-deoxy-D-arabino-2-heptulopyranosidonic acid 
• 119005-64-0 methyl onate 
• 119005-63-9 methyl onate 
• 119070-22-3 phenyl 2-deoxy-3,4,6-tris-O-(phenylmethyl)-1-thio-D-arabino-hexopyranoside 
• 119005-72-0 methyl <4,5,7-tri-O-benzyl-2,3-dideoxy-α-D-arabino-2-heptulopyranosid>onate 
• 120851-99-2 methyl onate 
• 119005-60-6 (4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 91780-35-7 chloro-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranoside 

Relevant academic research and scientific papers

Aluminium triflate catalysed O-glycosidation: Temperature-switched selective Ferrier rearrangement or direct addition with alcohols

A temperature-controlled mechanism switch between the Al(OTf) 3-catalysed direct addition of alcohols or the Ferrier rearrangement reactions in some glycals is presented. The scope and limitations are investigated as are the influence of the st

PROCESS FOR THE SYNTHESIS OF 2-DEOXY-D-GLUCOSE

The present invention provides a process for the synthesis of 2-deoxy-D-glucose comprising haloalkoxylation of R-D-Glucal wherein R is selected from H and 3, 4, 6-tri-O-benzyl, to obtain alkyl 2-deoxy-2-halo-R-α/β-D-gluco/mannopyranoside, converting alkyl

Diastereoselective Free-radical Reactions. Part 1. Preparation of 2-Deoxy-β-glycosides by Synthesis and Reductive Decarboxylation of 3-Deoxyulosonic Acid Glycosides

A general procedure for the synthesis of 2-deoxy-β-D-glycosides involving the preparation of 3-deoxyulosonic acid glycosides from glycals and their reductive decarboxylation is described.