405236-05-7

Upstream product

• 200052-99-9 (4aR,6S,7R,8R,8aR)-2,2-Dimethyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 824-94-2 p-methoxybenzyl chloride 
• 16758-34-2 1-thiophenyl-β-D-galactopyranoside 

Downstream Products

• 1225450-71-4 phenyl 6-O-benzoyl-2,3-di-O-(4-methoxyphenylmethyl)-1-thio-β-D-galactopyranoside 
• 405236-13-7 4-Methyl-benzoic acid (2S,3R,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-(2-chloro-acetoxy)-2-phenylsulfanyl-tetrahydro-pyran-3-yl ester 
• 405236-11-5 Chloro-acetic acid (2R,3S,4R,5R,6S)-3-benzyloxy-2-benzyloxymethyl-5-hydroxy-6-phenylsulfanyl-tetrahydro-pyran-4-yl ester 
• 405236-08-0 phenyl 4,6-di-O-benzyl-1-thio-β-D-galactopyranoside 

Relevant academic research and scientific papers

Synthesis of a trigalacturonic acid analogue mimicking the expected transition state in the glycosidases

A trigalacturonic acid analogue carrying a cyclohexene framework in place of the central pyranose ring was synthesized as a molecular probe for the mechanistic investigation of endo-polygalacturonase 1 (endo-PG 1). Preliminary enzymatic studies revealed t

Solid-phase capture-release strategy applied to oligosaccharide synthesis on a soluble polymer support

A highly simplified synthesis of a tetrasaccharide was possible by a repeated coupling/capture-release cycle. In the first cycle, a glycosyl acceptor (1) bound to a soluble polymer reacted with a glycosyl donor (2) having a chloroacetyl group as a tempora