366786-64-3

Upstream product

• 152612-42-5 (2S,5R)-1-tert-butoxycarbonyl-5-hydroxymethyl-2-benzyloxymethyl pyrrolidine 
• 366786-61-0 (2S,5S)-1-tert-butoxycarbonyl-2-tert-butyldimethylsilyloxymethyl-3-phenylsulfonyl-5-benzyloxymethyl pyrrolidine 
• 366786-62-1 (2S,5S)-1-tert-butoxycarbonyl-2-hydroxymethyl-3-phenylsulfonyl-5-benzyloxy-methyl pyrrolidine 
• 879572-80-2 (2R,5S)-5-(benzyloxymethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid 
• 75-16-1 methylmagnesium bromide 
• 366786-63-2 (2S,5R)-1-tert-butoxycarbonyl-2-benzyloxymethyl-5-methoxycarbonyl-pyrrolidine 

Downstream Products

• 366786-65-4 (2S,5R)-1-tert-butoxycarbonyl-2-hydroxymethyl-5-(1'-hydroxy-1'-methylethyl)-pyrrolidine 

Relevant academic research and scientific papers

Facile synthesis of N-Boc-(2S,5R)-5-(1′-hydroxy-1′-methylethyl)proline

Coupling of chiral 1-O-benzylglycerol-2,3-bistriflate with trilithiated chiral 2-N-Boc-3-phenylsulfonylpropan-1-ol derivative constitutes an efficient route to chiral C-5 substituted prolines which can potentially induce cis Xaa-Pro peptide bond conformation. A straightforward seven-step synthesis of the title compound is described.