Výsledky vyhledávání - "Morgan Donnard"

(NHC-olefin)-nickel(0) nanoparticles as catalysts for the (Z)-selective semi-hydrogenation of alkynes and ynamides

Autor: Marta G. Avello, Stéphane Golling, Lai Truong-Phuoc, Loïc Vidal, Thierry Romero, Vasiliki Papaefthimiou, Nathalie Gruber, Michael J. Chetcuti, Frédéric R. Leroux, Morgan Donnard, Vincent Ritleng, Cuong Pham-Huu, Christophe Michon

Publikováno v: Chemical Communications
Chemical Communications, 2022, ⟨10.1039/D2CC05302K⟩

International audience; Nickel(0) nanoparticles coordinated to NHC ligands bearing a N-coordinated cynnamyl moiety were readily prepared by reduction of a [NiCpBr(NHC-cynnamyl)] complex with methyl magnesium bromide. The combination of a strong sigma

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da6eb6e24102eb161dfe6a2d8dadadbd
https://hal.archives-ouvertes.fr/hal-03909675/file/manuscript_HAL_ChemCommun2023_CMichon.pdf

Zobrazit plný text záznamu

Direct Access to 2,3-Disubstituted Amido-Indenones through Annulation of 2-Iodobenzaldehydes with Ynamides

Autor: Stéphane Golling, Pierre Hansjacob, Nassim Bami, Frédéric R. Leroux, Morgan Donnard

Publikováno v: The Journal of organic chemistry.

In this paper we report the annulation reaction between 2-iodobenzaldehyde derivatives and various ynamides. This palladium-catalyzed reaction leads to rare polysubstituted amino-indenones in good yields with a regioselectivity up to complete. Remark

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c474f7a5b88b298fd208650b9052a556
https://pubmed.ncbi.nlm.nih.gov/36472915

Zobrazit plný text záznamu

Versatile Access to Tetrasubstituted 2-Amidoacroleins through Formal Silylformylation of Ynamides

Autor: Morgan Donnard, Stéphane Golling, Frédéric R. Leroux

Publikováno v: Organic Letters
Organic Letters, American Chemical Society, 2021, ⟨10.1021/acs.orglett.1c03141⟩

International audience; In this paper we are reporting the first regio-and stereo-selective silylformylation of ynamides. This reaction is tolerant to a wide range of functional groups around the ynamides. The substitution of CO by an isocyanide make

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9abd73d4fcb775d2e409a3e44ab1e69
https://doi.org/10.1021/acs.orglett.1c03141

Zobrazit plný text záznamu

Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study

Autor: Agnieszka Chylewska, Morgan Donnard, Marko V. Rodić, Predrag Ristić, Goran V. Janjić, Mariusz Makowski, Vladimir A. Blagojević, Mihaela Gulea, Tamara R. Todorović, Nenad Filipovic, Predrag Vulić

Publikováno v: Crystal Growth & Design
Crystal Growth & Design, American Chemical Society, 2020, 20 (5), pp.3018-3033. ⟨10.1021/acs.cgd.9b01661⟩

Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a671a2b7b7786057633ecd4fa4fbe0c1
https://doi.org/10.1021/acs.cgd.9b01661

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání