Ontology highlight
ABSTRACT:
SUBMITTER: Yanev P
PROVIDER: S-EPMC6204755 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature
Beilstein journal of organic chemistry 20181010
Ethylenediamine-derived β-enamino amides are used as equivalents of amide enolate synthons in <i>C</i>-acylation reactions with <i>N</i>-protected amino acids. Domino fragmentation of the obtained intermediates leads to functionalised β-keto amides, bearing a protected amino group in their side chain. ...[more]