172297-69-7

Upstream product

• 117252-95-6 2-(trimethylsilyl)ethyl β-D-galactopyranoside 
• 172297-67-5 2-(trimethylsilyl)ethyl 2,3-di-O-tertbutyldimethylsilyl-β-D-galactopyranoside 
• 172297-66-4 2-(trimethylsilyl)ethyl 4,6-O-benzylidene-2,3-di-O-tertbutyldimethylsilyl-β-D-galactopyranoside 
• 117252-96-7 2-(trimethylsilyl)ethyl 4,6-di-O-benzylidene-β-D-galactopyranoside 
• 76-83-5 trityl chloride 
• 172297-68-6 2-(trimethylsilyl)ethyl 2,3-di-O-tertbutyldimethylsilyl-6-O-triphenylmethyl-β-D-galactopyranoside 

Downstream Products

• 172297-70-0 2-(trimethylsilyl)ethyl 2,3-di-O-tertbutyldimethylsilyl-4-C-methyl-6-O-triphenylmethyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of 2-(trimethylsilyl)ethyl 4-C-methyl-β-D-glucopyranuronamide. A derivative suitable as building block in synthesis of phosphoglycolipid antibiotics

The title compound, a protected derivative of a unique component in the moenuronamide group of phosphoglycolipid antibiotics has been synthesised in eleven steps and 30% total yield from 2-(trimethylsilyl)ethyl-β-D-galactopyranoside (6). The key step was