1234477-03-2Relevant academic research and scientific papers
Synthesis of new protected azahistidine, their processes and their use in synthesises
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Page/Page column 8; 10-11, (2010/08/07)
The synthesis of various protected azahistidine derivatives are obtained via 1,3-dipolar cycloaddition reactions. The newly obtained amino acids can in particular be selectively deprotected either at the side chain or at the N-terminus of the amino acid a
Synthesis of orthogonally protected azahistidine: Application to the synthesis of a GHK analogue
Roux, Stephane,Ligeti, Melinda,Buisson, David-Alexandre,Rousseau, Bernard,Cintrat, Jean-Christophe
experimental part, p. 279 - 286 (2010/08/21)
The synthesis of various orthogonally protected azahistidine derivatives are obtained via 1,3-dipolar cycloaddition reactions. The newly obtained amino-acids can be selectively deprotected either at the side chain or at the N-terminus of the amino acid and should thus allow the use of these derivatives in (solid phase) peptide synthesis.
