Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Héctor Fernández-Pérez"'
Publikováno v:
European Journal of Organic Chemistry. 2020:4331-4338
Publikováno v:
Organic Letters. 21:7019-7023
A highly stereoselective catalytic method for the preparation of structurally diverse P-stereogenic oxides has been developed. The approach relies on the ability of rhodium complexes derived from a...
Autor:
Andrés Romero-Navarro, Alicia Martínez-Carrión, Nuria Llorente, Alba Martínez-Bascuñana, José Luis Núñez-Rico, Lucas Carreras, Anton Vidal-Ferran, Ester Iniesta, Héctor Fernández-Pérez
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat. Dipósit de la Recerca de Catalunya
instname
Over several years, our research team has contributed to ligand design for metal-catalyzed stereoselective transformations. This has been achieved with the synthesis and application to organic transformations of interest of an array of structurally d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c40ff1a493a1b7353535ebda8cc5526
http://hdl.handle.net/2072/357525
http://hdl.handle.net/2072/357525
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
instname
Herein is reported the effect of different polyether binders (alkali metal, alkaline earth metal and lanthanide salts) as regulation agents to enhance the catalytic properties of palladium complexes derived from enantiopure bisphosphite ligands in al
Autor:
Arnald Grabulosa, Héctor Fernández-Pérez, Lucas Carreras, Paweł Kafarski, Paweł Lenartowicz, Anton Vidal-Ferran
Publikováno v:
Journal of Organic Chemistry. 85(22):14779−14784
The hydrogenation of N-substituted vinylphosphonates using rhodium complexes derived from P–OP ligands L1, ent-L1, or (R,R)-Me-DuPHOS as catalysts has been successfully accomplished, achieving very high levels of stereoselectivity (up to 99% ee or
Publikováno v:
RECERCAT (Dipòsit de la Recerca de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat. Dipósit de la Recerca de Catalunya
instname
Detailed investigations on the use of nickel(0)-based catalysts for intramolecular [4+4]-cycloadditions are presented. Nickel(0) complexes derived from electron-rich triarylphosphines proved to be efficient catalysts for intramolecular [4+4]- cycload
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b24ba29e9496f5cb5207486c8c28297
https://hdl.handle.net/2072/355958
https://hdl.handle.net/2072/355958
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
instname
Enantiopure sulfoxides are valuable precursors of organosulfur compounds with a broad application in organic and pharmaceutical chemistry. An unprecedented strategy for obtaining highly enantioenriched sulfoxides based on a hydrogenative kinetic reso
Publikováno v:
Tetrahedron. 71:4490-4494
Herein is reported the efficient preparation of a set of enantiopure bisphosphine ligands, whose backbone incorporates an array of diverse crown ethers as distal regulation sites via well-defined supramolecular interactions to tune the catalytic prop
Autor:
Bugga Balakrishna, José Luis Núñez-Rico, Anton Vidal-Ferran, Pablo Etayo, Héctor Fernández-Pérez
Publikováno v:
RSC Adv.. 4:58440-58447
Various oxa-containing heterocycles (i.e. enantiopure epoxide- and oxetane-based substrates) were subjected to ring-opening with phosphorus nucleophiles. The ring-opening reactions proceeded smoothly and the resulting 1,2-, and 1,3-phosphino alcohols
Publikováno v:
Organic Letters. 15:3634-3637
A series of small bite-angle phosphine-phosphite (P-OP) ligands have been synthesized by a two-step method. The key intermediate was prepared by an unprecedented asymmetric carbonyl reduction of a phosphamide using the CBS (Corey-Bakshi-Shibata) cata