1055032-87-5

Upstream product

• 162613-15-2 Ethyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-β-D-glucopyranoside 
• 162681-47-2 ethyl 2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 141810-60-8 ethyl 3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 

Downstream Products

• 1053632-38-4 (2S,3S,4S,5R,6R)-3,4-Bis-benzyloxy-6-((2R,4aR,6S,7S,8S,8aR)-8-benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy)-5-(2,2-dimethyl-propionyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 162613-19-6 Methyl (ethyl 3,4-di-O-benzyl-2-O-(p-methoxybenzoyl)-1-thio-β-D-glucopyranosid)uronate 
• 162613-18-5 Methyl (ethyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-β-D-glucopyranosid)uronate 
• 162613-20-9 Methyl (ethyl 3,4-di-O-benzyl-2-O-pivaloyl-1-thio-β-D-glucopyranosid)uronate 
• 162613-17-4 Methyl (ethyl 3,4-di-O-benzyl-1-thio-β-D-glucopyranosid)uronate 
• 162613-16-3 Methyl (ethyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-β-D-glucopyranosid)uronate 

Relevant academic research and scientific papers

Synthesis of Methyl (Ethyl 2-O-acyl-3,4-di-O-benzyl-1-thio-β-D-glucopyranosid)uronates and Evaluation of Their Use as Reactive β-Selective Glucuronic Acid Donors

The synthesis of derivatives of methyl (ethyl 2-O-acyl-3,4-di-O-benzyl-1-thio-β-D-glucopyranosid)uronate with different ester groups (acetyl, benzoyl, pivaloyl, and anisoyl) at O-2 is described.The synthesis proceeds via a two-step oxidation (DMSO/DCC fol