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Peer-reviewedCC BY-NC 3.0RSC Advances

Synthesis of 5-[3-amino-imidazo[1,2- a ]pyridin-6-yl]pyridin-2-ones and derivatives through the combination of palladium-catalyzed cross-coupling and GBB multi-component reactions

  1. 1Université d’Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France
  2. 2Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301 Av. de la Terrasse 91198 Gif-sur-Yvette France

Abstract

A combined Suzuki-type palladium-catalyzed cross-coupling and Groebke–Blackburn–Bienaymé (GBB) multicomponent strategy enabled the synthesis of novel 5-[3-amino-imidazo[1,2- a ]pyridin-6-yl]pyridin-2-ones and 3,5-disubstituted pyridin-2-ones.

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BibTeX
@article{caillet2026synthesis,
  title = {{Synthesis of 5-[3-amino-imidazo[1,2- a ]pyridin-6-yl]pyridin-2-ones and derivatives through the combination of palladium-catalyzed cross-coupling and GBB multi-component reactions}},
  author = {Emma Caillet and Quentin Chevrier and Pascal Retailleau and Sabine Berteina-Raboin and Isabelle Gillaizeau},
  journal = {RSC Advances},
  year = {2026},
  month = oct,
  doi = {10.1039/d6ra03865d},
  url = {https://hal.science/hal-05842127v1},
  note = {CC BY-NC 3.0},
}
RIS
TY  - JOUR
TI  - Synthesis of 5-[3-amino-imidazo[1,2- a ]pyridin-6-yl]pyridin-2-ones and derivatives through the combination of palladium-catalyzed cross-coupling and GBB multi-component reactions
AU  - Emma Caillet
AU  - Quentin Chevrier
AU  - Pascal Retailleau
AU  - Sabine Berteina-Raboin
AU  - Isabelle Gillaizeau
PY  - 2026
DA  - 2026/10/08
JO  - RSC Advances
DO  - 10.1039/d6ra03865d
UR  - https://hal.science/hal-05842127v1
AB  - A combined Suzuki-type palladium-catalyzed cross-coupling and Groebke–Blackburn–Bienaymé (GBB) multicomponent strategy enabled the synthesis of novel 5-[3-amino-imidazo[1,2- a ]pyridin-6-yl]pyridin-2-ones and 3,5-disubstituted pyridin-2-ones.
SN  - 2046-2069
ER  -