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  • Nucleophilic substitution of protected 2-amino-4-butanoic acid. An easy route to exotic amino acids and conformationally constrained peptides

  • Add time:07/28/2019    Source:sciencedirect.com

    The synthesis of a series of novel α-amino acids based on the nucleophilic substitution of protected 2-amino-4-bromobutanoic acid (1) is described. Basic, acidic or neutral amino acids can be obtained; chimerical amino acids carrying a coenzyme type structure in the side chain, multifunctional amino acids for the synthesis of cross-linked peptides or dendrimers and conformationally constrained peptides can also be obtained.

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    Prev:[2.2.2]propellane rearrangements
    Next:Synthesis of N-Fmoc-α-amino acids carrying the four DNA nucleobases in the side chain.)

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