The monoalkylating and enantioselective behaviour of a chiral 2-bromoamide allows the synthesis of pseudopeptides in which a dipeptide component is changed into an aminodicarboxy moiety, with overall retention of configuration.
2-Bromoamides as Synthons for Pseudopeptides Containing Aminodicarboxy Units
MARCHETTI, Paolo;SALVADORI, Severo;
1993
Abstract
The monoalkylating and enantioselective behaviour of a chiral 2-bromoamide allows the synthesis of pseudopeptides in which a dipeptide component is changed into an aminodicarboxy moiety, with overall retention of configuration.File in questo prodotto:
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