404351-12-8

Upstream product

• 131564-36-8 ethyl (S)-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 147332-52-3 ethyl 2,3-di-O-acetyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 

Downstream Products

• 404351-14-0 ethyl 2,4-di-O-benzoyl-6-O-benzyl-3-O-chloroacetyl-1-thio-β-D-galactopyranoside 
• 404351-13-9 ethyl 2,4-di-O-benzoyl-6-O-benzyl-1-thio-β-D-galactopyranoside 
• 116167-60-3 S-ethyl-6-O-(phenylmethyl)-1-thio-β-D-galactopyranoside 

Relevant academic research and scientific papers

Regioselective reductive ring opening of benzylidene acetals using triethylsilane and iodine

Novel reaction conditions have been developed for the regioselective reductive ring opening of benzylidene acetals in carbohydrate derivatives using triethylsilane and molecular iodine. The reaction is fast, compatible with most of the functional groups e

An efficient and stereoselective synthesis of β-D-Arap-(1 → 2)-β-D-Galp-(1 → 3)-β-D-Galp-(1 → 4)-α-D-Manp, a tetrasaccharide fragment of Leishmania major lipophosphoglycan

A tetrasaccharide fragment of Leishmania major lipophosphoglycan (which seems to be involved in a biological mechanism for the parasite transmission) has been synthesised using the thioglycoside, trichloroacetimidate and halide-exchange glycosylation procedures and step-wise chain elongation strategy.