Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Marc Montesinos-Magraner"'
Publikováno v:
Handbook of CH‐Functionalization. :1-21
Autor:
Giuseppe Zuccarello, Leonardo J. Nannini, Ana Arroyo-Bondía, Nicolás Fincias, Isabel Arranz, Alba H. Pérez-Jimeno, Matthias Peeters, Inmaculada Martín-Torres, Anna Sadurní, Víctor García-Vázquez, Yufei Wang, Mariia S. Kirillova, Marc Montesinos-Magraner, Ulysse Caniparoli, Gonzalo D. Núñez, Feliu Maseras, Maria Besora, Imma Escofet, Antonio M. Echavarren
A new generation of chiral gold(I) catalysts based on variations of complexes with JohnPhos-type ligands with a remote C2-symmetric 2,5-diarylpyrrolidine have been synthesized with different substitutions at the top and bottom aryl rings: from replac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d065572de737b71d6aa7b772e972624e
https://doi.org/10.26434/chemrxiv-2023-vxlcf
https://doi.org/10.26434/chemrxiv-2023-vxlcf
Autor:
Amparo Sanz-Marco, Daniel Esperilla, Marc Montesinos-Magraner, Carlos Vila, M. Carmen Muñoz, José R. Pedro, Gonzalo Blay
Publikováno v:
Sanz Marco, Amparo Esperilla, Daniel Montesinos Magraner, Marc Vila Descals, Carlos Muñoz, M. Carmen Pedro, José Ramón Blay Llinares, Gonzalo 2023 A Cu-BOX catalysed enantioselective Mukaiyama-aldol reaction with difluorinated silyl enol ethers and acylpyridine N-oxides Organic & Biomolecular Chemistry 21 2 345 350
A Cu(II)/BOX complex catalyses the enantioselective addition of difluorinated silyl enol ethers to acylpyridine N-oxides. The reaction provides difluorinated chiral tertiary alcohols of great interest in medicinal chemistry. These compounds are obtai
Autor:
Amparo Sanz Marco, Carlos Vila Descals, Marc Montesinos Magraner, Alicia Monleón Ventura, Gonzalo Blay Llinares, Luz Cardona Prosper, Isabel Fernández Picot, José Ramón Pedro Llinares
[EN] The importance of the Sustainable Development Goals (SDGs) and their necessary implementation in the University environment drives us to develop innovative projects for the dissemination and implementation of the SDGs in the Chemistry Degree at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3ca01cfd7193ce1f7823a9e287dc573
https://doi.org/10.4995/inred2022.2022.15910
https://doi.org/10.4995/inred2022.2022.15910
Publikováno v:
European Journal of Organic Chemistry. 2022
Publikováno v:
European journal of organic chemistry. 2022(38)
H-bonded counterion-directed catalysis (HCDC) is a strategy wherein a chiral anion that is hydrogen-bonded to the achiral ligand of a metal complex is responsible for enantioinduction. In this article we present the application of H-bonded counterion
Autor:
Eric Tan, Marc Montesinos-Magraner, Antonio M. Echavarren, Cristina García-Morales, Joan Guillem Mayans
Publikováno v:
Chemical Science. 12:14731-14739
The ortho-alkynylation of nitro-(hetero)arenes takes place in the presence of a Rh(III) catalyst to deliver a wide variety of alkynylated nitroarenes regioselectively. These interesting products could be further derivatized by selective reduction of
Publikováno v:
Organic Letters. 22:5380-5384
A straightforward strategy for the synthesis of unprecedented α-aminoperoxides bearing primary and secondary alkylperoxide substituents is described. Commercially available dialkylzinc reagents are oxidized with molecular oxygen and the consequent p
Autor:
Eric, Tan, Marc, Montesinos-Magraner, Cristina, García-Morales, Joan Guillem, Mayans, Antonio M, Echavarren
Publikováno v:
Chemical Science
The ortho-alkynylation of nitro-(hetero)arenes takes place in the presence of a Rh(iii) catalyst to deliver a wide variety of alkynylated nitroarenes regioselectively. These interesting products could be further derivatized by selective reduction of
Autor:
Rodrigo Ramírez‐Contreras, Marc Montesinos-Magraner, Michael E. Muratore, Abraham Mendoza, Magnus Johansson, Matteo Costantini
Publikováno v:
Angewandte Chemie International Edition
Asymmetric cyclopropane synthesis currently requires bespoke strategies, methods, substrates, and reagents, even when targeting similar compounds. This approach slows down discovery and limits available chemical space. Introduced herein is a practica