762267-53-8

Downstream Products

• 762267-61-8 (S)-2-{(S)-2-[2-((2S,3S,6S)-2-Allyloxy-6-azidomethyl-3,6-dihydro-2H-pyran-3-yl)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid methyl ester 
• 762267-60-7 (S)-2-{(S)-2-[2-((2S,3S,6S)-2-Allyloxy-6-azidomethyl-3,6-dihydro-2H-pyran-3-yl)-acetylamino]-3-phenyl-propionylamino}-4-methylsulfanyl-butyric acid methyl ester 
• 762267-66-3 (S)-2-{(S)-2-[2-((2S,3S,6S)-2-Allyloxy-6-azidomethyl-3,6-dihydro-2H-pyran-3-yl)-acetylamino]-3-phenyl-propionylamino}-N-methyl-4-methylsulfanyl-butyramide 
• 1207071-22-4 C₂₇H₃₂Cl₃NO₄Si 
• 1207071-23-5 C₂₇H₃₂Cl₃NO₄Si 
• 1207071-24-6 C₂₅H₃₁ClO₃Si 
• 1403603-22-4 C₂₈H₃₈O₆SSi 
• 1403603-21-3 C₂₇H₃₆O₄Si 
• 1403603-27-9 C₂₉H₄₁NO₅Si 
• 1403603-31-5 C₂₉H₄₁NO₅Si 
• 1403603-26-8 C₂₅H₂₃N₅O₁₃ 

Relevant academic research and scientific papers

Preparation of sugar amino acids by Claisen-Johnson rearrangement: Synthesis and incorporation into enkephalin analogues

We have developed a convenient route for the synthesis of an unsaturated branched sugar bearing a carboxylic acid and an amino group (masked as an azide group) by employing a totally stereoselective Claisen-Johnson rearrangement as the key step. Several M