Oudeyer S - Search Results

1

Organocatalytic Strategy for a Formal 1,6-Conjugate Hydroxylation.

Aouina SM, Lapray A, Naubron JV, Vanthuyne N, Levacher V, Oudeyer S, Perrio S, Brière JF. Aouina SM, et al. Among authors: oudeyer s. Org Lett. 2024 Nov 1;26(43):9294-9298. doi: 10.1021/acs.orglett.4c03482. Epub 2024 Oct 18. Org Lett. 2024. PMID: 39423144

2

Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.

Fall A, Magdei M, Savchuk M, Oudeyer S, Beucher H, Brière JF. Fall A, et al. Among authors: oudeyer s. Chem Commun (Camb). 2024 Jun 13;60(49):6316-6319. doi: 10.1039/d4cc01766h. Chem Commun (Camb). 2024. PMID: 38819219

3

Vinylogous and stereoselective domino synthesis of pyrano[2,3-c]pyrroles from alkylidene meldrum's acids.

Savchuk M, Vo-Thanh G, Oudeyer S, Beucher H, Brière JF. Savchuk M, et al. Among authors: oudeyer s. Org Biomol Chem. 2024 Apr 17;22(15):2948-2952. doi: 10.1039/d4ob00233d. Org Biomol Chem. 2024. PMID: 38482880

4

Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives.

Maret C, David N, Pierrot D, Léonel E, Levacher V, Brière JF, Oudeyer S. Maret C, et al. Among authors: oudeyer s. Molecules. 2023 Sep 20;28(18):6704. doi: 10.3390/molecules28186704. Molecules. 2023. PMID: 37764480 Free PMC article.

5

An Organocatalytic and Stereoselective Vinylogous Domino Process towards Thiochromans.

Milbeo P, Lebrêne A, Savchuk M, Vo-Thanh G, Oudeyer S, Beucher H, Brière JF. Milbeo P, et al. Among authors: oudeyer s. Chemistry. 2023 Jul 26;29(42):e202301311. doi: 10.1002/chem.202301311. Epub 2023 Jun 19. Chemistry. 2023. PMID: 37184891

6

Recent Advances in Catalytic and Technology-Driven Radical Addition to N,N-Disubstituted Iminium Species.

Oudeyer S, Levacher V, Beucher H, Brière JF. Oudeyer S, et al. Molecules. 2023 Jan 20;28(3):1071. doi: 10.3390/molecules28031071. Molecules. 2023. PMID: 36770738 Free PMC article. Review.

7

Diastereoselective addition of redox active esters to azomethine imines by electrosynthesis.

Leleu L, Martzel T, Fall A, Sanselme M, Levacher V, Oudeyer S, Brière JF. Leleu L, et al. Among authors: oudeyer s. Chem Commun (Camb). 2022 May 20;58(41):6100-6103. doi: 10.1039/d2cc01795d. Chem Commun (Camb). 2022. PMID: 35503100

8

The Catalytic Regio- and Stereoselective Synthesis of 1,6-Diazabicyclo[4.3.0]nonane-2,7-diones.

Lebrêne A, Martzel T, Gouriou L, Sanselme M, Levacher V, Oudeyer S, Afonso C, Loutelier-Bourhis C, Brière JF. Lebrêne A, et al. Among authors: oudeyer s. J Org Chem. 2021 Jul 2;86(13):8600-8609. doi: 10.1021/acs.joc.1c00252. Epub 2021 Jun 14. J Org Chem. 2021. PMID: 34125536

9

Alkylidene Meldrum's Acids as Platforms for the Vinylogous Synthesis of Dihydropyranones.

Wittmann S, Martzel T, Pham Truong CT, Toffano M, Oudeyer S, Guillot R, Bournaud C, Gandon V, Brière JF, Vo-Thanh G. Wittmann S, et al. Among authors: oudeyer s. Angew Chem Int Ed Engl. 2021 May 10;60(20):11110-11114. doi: 10.1002/anie.202014489. Epub 2021 Apr 6. Angew Chem Int Ed Engl. 2021. PMID: 33667024

10

Organocatalytic Multicomponent Synthesis of α/β-Dipeptide Derivatives.

Martzel T, Annibaletto J, Millet P, Pair E, Sanselme M, Oudeyer S, Levacher V, Brière JF. Martzel T, et al. Among authors: oudeyer s. Chemistry. 2020 Jul 14;26(39):8541-8545. doi: 10.1002/chem.202001214. Epub 2020 Jun 18. Chemistry. 2020. PMID: 32160344

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