Folgen
Marc Magre
Titel
Zitiert von
Zitiert von
Jahr
Magnesium‐Catalyzed Hydroboration of Terminal and Internal Alkynes
M Magre, B Maity, A Falconnet, L Cavallo, M Rueping
Angewandte Chemie International Edition 58 (21), 7025-7029, 2019
1052019
s-Block metal catalysts for the hydroboration of unsaturated bonds
M Magre, M Szewczyk, M Rueping
Chemical Reviews 122 (9), 8261-8312, 2022
812022
Regiodivergent hydroborative ring opening of epoxides via selective C–O bond activation
M Magre, E Paffenholz, B Maity, L Cavallo, M Rueping
Journal of the American Chemical Society 142 (33), 14286-14294, 2020
642020
Asymmetric magnesium‐catalyzed hydroboration by metal‐ligand cooperative catalysis
A Falconnet, M Magre, B Maity, L Cavallo, M Rueping
Angewandte Chemie 131 (49), 17731-17735, 2019
572019
Redox-neutral organometallic elementary steps at bismuth: catalytic synthesis of aryl sulfonyl fluorides
M Magre, J Cornella
Journal of the American Chemical Society 143 (51), 21497-21502, 2021
552021
Asymmetric hydrogenation of disubstituted, trisubstituted, and tetrasubstituted minimally functionalized olefins and cyclic β-enamides with easily accessible Ir–P, oxazoline …
M Biosca, M Magre, O Pamies, M Dieguez
ACS Catalysis 8 (11), 10316-10320, 2018
432018
Reduction of cyclic and linear organic carbonates using a readily available magnesium catalyst
M Szewczyk, M Magre, V Zubar, M Rueping
ACS Catalysis 9 (12), 11634-11639, 2019
402019
Chemo- and Regioselective Magnesium-Catalyzed ortho-Alkenylation of Anilines
A Chatupheeraphat, M Rueping, M Magre
Organic letters 21 (22), 9153-9157, 2019
372019
PHOX-Based Phosphite-Oxazoline Ligands for the Enantioselective Ir-Catalyzed Hydrogenation of Cyclic β-Enamides
M Magre, O Pamies, M Dieguez
ACS Catalysis 6 (8), 5186-5190, 2016
372016
Conformational Preferences of a Tropos Biphenyl Phosphinooxazoline–a Ligand with Wide Substrate Scope
R Bellini, M Magre, M Biosca, PO Norrby, O Pamies, M Dieguez, ...
ACS Catalysis 6 (3), 1701-1712, 2016
342016
Chemoselective luche-type reduction of α, β-unsaturated ketones by magnesium catalysis
YK Jang, M Magre, M Rueping
Organic letters 21 (20), 8349-8352, 2019
322019
Alternatives to Phosphinooxazoline (t‐BuPHOX) Ligands in the Metal‐Catalyzed Hydrogenation of Minimally Functionalized Olefins and Cyclic β‐Enamides
M Biosca, M Magre, M Coll, O Pàmies, M Diéguez
Advanced Synthesis & Catalysis 359 (16), 2801-2814, 2017
322017
Filling the gaps in the challenging asymmetric hydroboration of 1, 1-disubstituted alkenes with simple phosphite-based phosphinooxazoline iridium catalysts
M Magre, M Biosca, O Pàmies, M Diéguez
ChemCatChem 7 (1), 114-120, 2015
322015
ZrCl 2 (η-C 5 Me 5) 2-AlHCl 2·(THF) 2: efficient hydroalumination of terminal alkynes and cross-coupling of the derived alanes
P Andrews, CM Latham, M Magre, D Willcox, S Woodward
Chemical Communications 49 (15), 1488-1490, 2013
322013
(Hetero)aryl‐SVI Fluorides: Synthetic Development and Opportunities
M Magre, S Ni, J Cornella
Angewandte Chemie International Edition 61 (23), e202200904, 2022
282022
N-Methylation and Trideuteromethylation of Amines via Magnesium-Catalyzed Reduction of Cyclic and Linear Carbamates
M Magre, M Szewczyk, M Rueping
Organic letters 22 (8), 3209-3214, 2020
272020
Magnesium-catalyzed stereoselective hydrostannylation of internal and terminal alkynes
M Magre, M Szewczyk, M Rueping
Organic letters 22 (4), 1594-1598, 2020
242020
Theoretical and experimental optimization of a new amino phosphite ligand library for asymmetric palladium‐catalyzed allylic substitution
M Magre, M Biosca, PO Norrby, O Pàmies, M Dieguez
ChemCatChem 7 (24), 4091-4107, 2015
242015
Extending the Substrate Scope for the Asymmetric Iridium‐Catalyzed Hydrogenation of Minimally Functionalized Olefins by Using Biaryl Phosphite‐Based Modular Ligand Libraries
O Pamies, M Magre, M Dieguez
The Chemical Record 16 (3), 1578-1590, 2016
232016
An improved class of phosphite-oxazoline ligands for Pd-catalyzed allylic substitution reactions
M Biosca, J Salto, M Magre, PO Norrby, O Pamies, M Dieguez
ACS Catalysis 9 (7), 6033-6048, 2019
222019
Das System kann den Vorgang jetzt nicht ausführen. Versuchen Sie es später erneut.
Artikel 1–20