4.8 Article

Visible-Light-Driven CarboxyLic Amine Protocol (CLAP) for the Synthesis of 2-Substituted Piperazines under Batch and Flow Conditions

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ORGANIC LETTERS
卷 22, 期 13, 页码 5157-5162

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c01759

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  1. Sanofi
  2. CNRS
  3. Chevreul Institute [FR 2638]
  4. Ministere de l'Enseignement Superieur et de la Recherche, Region Nord - Pas de Calais
  5. FEDER

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Piperazines are privileged scaffolds in medicinal chemistry. Disclosed herein is a visible-light-promoted decarboxylative annulation protocol between a glycine-based diamine and various aldehydes to access 2-aryl, 2-heteroaryl, as well as 2-alkyl piperazines. The iridium-based complex [Ir(ppy)(2)(dtbpy)]PF6 and carbazolyl dicyanobenzene 4CzIPN were found to be the photocatalysts of choice to efficiently perform the transformation under mild conditions, whether in batch or in continuous mode.

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