91797-40-9

Upstream product

• 75-16-1 methylmagnesium bromide 
• 113019-43-5 2,3,4,6-tetra-O-benzyl-1-formyl-D-glucopyranose 
• 100-39-0 benzyl bromide 
• 91738-16-8 1,3-Diphenyl-2-((2S,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-imidazolidine 
• 74281-68-8 3,4,5,7-Tetra-O-acetyl-2,6-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-D-glycero-D-gulo-heptose 
• 74-88-4 methyl iodide 

Downstream Products

• 91738-18-0 Toluene-4-sulfonic acid (S)-1-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-ethyl ester 
• 85230-64-4 4,5,6,8-Tetra-O-acetyl-3,7-anhydro-1-desoxy-2-O-(p-tolylsulfonyl)-D-erythro-L-talo-octitol 
• 85230-63-3 3,7-Anhydro-4,5,6,8-tetra-O-benzyl-1-desoxy-2-O-(p-tolylsulfonyl)-D-erythro-L-talo-octitol 

Relevant academic research and scientific papers

Synthesis of alkylated sugar amino acids: Conformationally restricted l-Xaa-l-Ser/Thr mimics

Two synthetic strategies for the generation of δ-substituted pyranoid sugar amino acids (SAAs) are evaluated. The first employs chiral nonracemic tert-butane sulfinamides as key reagents. Regardless of the stereochemistry of the applied sulfinamide, the p

Reactions of Enolic Sugar Derivatives, XVI. - Synthesis of a Diastereotopic Proton Probe for α- and β-D-Glucosylases

For the elucidation of the stereochemistry in glucosylase-catalyzed proton addition reactions (Z)-3,7-anhydro-1,2-dideoxy-D-gluco-oct-2-enitol (1) was synthesized.Starting material for the multistep synthesis is 3,4,5,7-tetra-O-acetyl-2,6-anhydro-1-C-(1,3