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Non-natural phenolic amino acids. Synthesis and application in peptide chemistry (CROSBI ID 114049)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Hutinec, Antun ; Ziogas, A. ; Rieker, Anton
Non-natural phenolic amino acids. Synthesis and application in peptide chemistry // Amino acids (Wien), 11 (1996), 3-4; 345-366-x
Podaci o odgovornosti
Hutinec, Antun ; Ziogas, A. ; Rieker, Anton
engleski
Non-natural phenolic amino acids. Synthesis and application in peptide chemistry
Several non-natural phenolic amino acids have been synthesized. t-Butylated tyrosine and thyroxine derivatives, on one-electron oxidation, give persistent radicals which can be used as positional and/or spin labels for amino acids. Two-electron oxidation of N-protected tyrosines leads to spirolactones, useful active esters for peptide coupling.
amino acids; spirolactones
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