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Nuno Monteiro
Researcher at Claude Bernard University Lyon 1
Publications - 111
Citations - 2335
Nuno Monteiro is an academic researcher from Claude Bernard University Lyon 1. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 28, co-authored 109 publications receiving 2227 citations. Previous affiliations of Nuno Monteiro include Lyon College & University of Lyon.
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Pd‐Assisted Multicomponent Synthesis of Heterocycles
TL;DR: In this paper, a review highlights some remarkable recently made achievements in the application of palladium-mediated processes to the design of multicomponent one-pot syntheses of heterocyclic compounds.
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Copper‐Catalyzed Trifluoromethylation of N,N‐Dialkylhydrazones
TL;DR: In this paper, a mild procedure for the conversion of N,N-dialkylhydrazones of aromatic aldehydes to the corresponding trifluoromethyl ketohydrazones is developed based on the use of the readily available hypervalent iodine reagent (II).
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Cyclisations involving attack of carbo- and heteronucleophiles on carbon-carbon π-bonds activated by organopalladium complexes
TL;DR: In the late 1980's, a new process based on an intramolecular palladium-mediated cyclisation coupled with a carbon-carbon bond forming reaction appeared in the literature as mentioned in this paper.
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Functionalized acetylenes as versatile building-blocks for the multicomponent assembling of polysubstituted furans and pyrroles
TL;DR: In this article, the versatility of functionalized alkynes in the multicomponent construction of polysubstituted furan and pyrrole derivatives is highlighted, and a review highlights the usefulness of functionalised alkynes.
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Palladium-mediated three-component synthesis of furo[2,3-b]pyridones by one-pot coupling of 3-iodopyridones, alkynes, and organic halides.
TL;DR: The one-pot assembly of 4-alkoxy-3-iodo-2-pyridones, terminal alkynes, and organic halides has been achieved by integration of two sequential palladium-mediated cross-coupling reactions--Sonogashira and Wacker-type heteroannulation processes--and subsequent deprotection of the alkoxy group to afford furo[2,3-b]pyrids.