Repurposing amine and carboxylic acid building blocks with an automatable esterification reaction.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
24 Jan 2023
Historique:
pubmed: 5 1 2023
medline: 5 1 2023
entrez: 4 1 2023
Statut: epublish

Résumé

New methodologies to unite amines and carboxylic acids that complement the popular amide coupling can significantly expand accessible chemical space if they yield products distinct from the classic R-NHC(O)-R' amide arrangement. Here we have developed an amine-acid esterification reaction based on pyridinium salt activation of amine C-N bonds to create products of type R-OC(O)-R' upon reaction with alkyl and aryl carboxylic acids. The protocol is robust and facile as demonstrated by automation on open-source robotics.

Identifiants

pubmed: 36598511
doi: 10.1039/d2cc05670d
doi:

Substances chimiques

Amines 0
Carboxylic Acids 0
Amides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1026-1029

Auteurs

Andrew McGrath (A)

Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, USA. tcernak@med.umich.edu.

Rui Zhang (R)

Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.

Khadija Shafiq (K)

Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, USA. tcernak@med.umich.edu.

Tim Cernak (T)

Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, USA. tcernak@med.umich.edu.
Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.

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Classifications MeSH