Synthesis of orthogonally protected azahistidine: Application to the synthesis of a GHK analogue
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.
Synthesis of new protected azahistidine, their processes and their use in synthesises
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
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Page/Page column 8; 10-11
(2010/08/07)
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