61236-89-3

Upstream product

• 37111-85-6 2,4,6-tri-O-benzyl-L-allose 
• 108-24-7 acetic anhydride 
• 3396-99-4 methyl α-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 129165-07-7 methyl 3-O-allyl-2,4,6-tri-O-benzyl-alpha-D-galactopyranoside 
• 84553-76-4 3-O-allyl-2,4,6-tri-O-benzyl-α,β-D-galactopyranoside 
• 129165-06-6 methyl 3-O-allyl-α-D-galactopyranoside 
• 37111-85-6 2,4,6-tri-O-benzyl-α,β-D-galactopyranose 

Downstream Products

• 129165-09-9 1,3-anhydro-2,4,6-tri-O-benzyl-β-D-galactopyranose 
• 129165-08-8 2,4,6-tri-O-benzyl-α-D-galactopyranosyl chloride 
• 127873-80-7 3-O-acetyl-2,4,6-tri-O-benzyl-D-glycopyranose 
• 89068-06-4 Acetic acid (2R,3R,4S,5R,6R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((2S,3S,4S,5R,6R)-2,3,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-4-yl ester 
• 89068-07-5 Acetic acid (2R,3R,4S,5R,6S)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((2S,3S,4S,5R,6R)-2,3,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-4-yl ester 
• 89068-05-3 3-O-acetyl-2,4,6-tri-O-benzyl-α-D-glucopyranosyl chloride 
• 120424-73-9 3-O-acetyl-2,4,6-tri-O-benzyl-α-D-galactopyranosyl chloride 

Relevant academic research and scientific papers

Direct amino acid catalyzed asymmetric synthesis of polyketide sugars

Back to the future: In a biomimetic asymmetric synthesis of sugars (see scheme) sequential cross-aldol reactions of simple aldehydes were catalyzed by amino acids. Deoxysugars were obtained with excellent chemoselectivity and up to > 99% ee. This transfor