762267-53-8Relevant articles and documents
Preparation of sugar amino acids by Claisen-Johnson rearrangement: Synthesis and incorporation into enkephalin analogues
Montero, Ana,Mann, Enrique,Herradon, Bernardo
, p. 3063 - 3073 (2004)
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