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Org Lett ; 23(11): 4168-4172, 2021 06 04.
Artículo en Inglés | MEDLINE | ID: mdl-34014099

RESUMEN

An umpolung reaction with α-hydrazonoesters was investigated, and it was found that α-N,N-dialkylaminoamides could be directly synthesized in yields up to 92% via a concomitant rearrangement of dialkylamino groups. As an application, a short synthesis of an inhibitor of glycine type-1-transporter was accomplished via subsequent functional group transformations in 28% overall yield.

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