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
- 1Université d’Orléans, CNRS, UMR 7311, ICOA 45067 Orléans France
- 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 -