84553-71-9

Upstream product

• 4304-12-5 benzyl β-D-galactopyranoside 
• 100-51-6 benzyl alcohol 
• 152088-86-3 benzyl 2,4,6-tri-O-benzoyl-3-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-galactopyranoside 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 56341-65-2 Benzyl 4,6-O-benzylidene-β-D-galactopyranoside 
• 84553-70-8 benzyl 4,6-O-benzylidene-3-O-β-D-galactopyranosyl-β-D-galactopyranoside 
• 84558-11-2 benzyl 2-O-acetyl-4,6-O-benzylidene-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-galactopyranoside 
• 120095-02-5 Acetic acid (2R,3R,4S,5S,6R)-3,5-diacetoxy-2-benzyloxy-6-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-tetrahydro-pyran-4-yl ester 
• 120095-01-4 Acetic acid (2R,3R,4S,5S,6R)-5-acetoxy-6-acetoxymethyl-2-benzyloxy-4-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester 

Downstream Products

• 120095-01-4 Acetic acid (2R,3R,4S,5S,6R)-5-acetoxy-6-acetoxymethyl-2-benzyloxy-4-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester 
• 584-30-5 3-O-β-galactopyranosyl-D-galactose 

Relevant academic research and scientific papers

Porcine liver (2 → 3)-α-sialyltransferase: Substrate specificity studies and application of the immobilized enzyme to the synthesis of various sialylated oligosaccharide sequences

In search of substrate analogues for the porcine liver β-D-Galp-(1 → 3)-D-Galp-NAc: CMP-Neu5Ac-(2 → 3')-α-sialyltransferase, three disaccharides β-D-Galp-(1→3)-β-D-Gal p-O-CH3 (5), β-D-Galp-(1→3)-β-D-(2-OAc)-Gal p-O-CH3 (7) and β-D-G

A SIMPLE STRATEGY FOR CHANGING THE REGIOSELECTIVITY OF GLYCOSIDASE-CATALYSED FORMATION OF DISACCHARIDES: PART II, ENZYMIC SYNTHESIS in situ OF VARIOUS ACCEPTOR GLYCOSIDES

β-D-Galactosidase induced the formation of allyl, benzyl, and trimethylsilylethyl β-D-galactopyranosides on a 1-20-g scale from lactose and allyl alcohol, benzyl alcohol, and trimethylsilylethanol, respectively.Similarly, α-D-galactosidase catalysed the formation of allyl α-D-galactopyranoside from raffinose and allyl alcohol.The galactosides were used as acceptors for the preparation of the following disaccharide glycosides: β-D-Gal-(1->3)-β-D-Gal-OCH2CH=CH2, β-D-Gal-(1->6)-β-D-Gal-OCH2CH=CH2, β-D-Gal-(1->3)-β-D-Gal-OBn, β-D-Gal-(1->6)-β-D-Gal-OBn, β-D-Gal-(1->3)-β-D-Gal-OCH2CH2SiMe3, and α-D-Gal-(1->3)-α-D-Gal-OCH2CH=CH2.The β-D-galactosidase-catalysed reactions were efficient enough to allow the one pot preparation of the various β-linked mono- and digalactosides from lactose and alcohol.