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Synthesis of ketomethylene amino pseudopeptide analogues via reductive amination of glyoxals derived from alpha-amino acids
Authors:Groarke M  Hartzoulakis B  McKervey M A  Walker B  Williams C H
Affiliation:School of Chemistry, The Queen's University, Belfast, UK.
Abstract:The reductive amination of an amino acid derived glyoxal, with the free amino group of a protected amino acid or oligopeptide fragment, has been developed as a simple and efficient method for the preparation of ketomethylene amino pseudo-oligopeptide isosteres Aa psi(COCH2NH)Aa. Trichlorosilane-DMF is the reagent of choice for the reduction.
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