Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Eva Rivera Chao"'
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
Angewandte Chemie (International Ed. in English)
instname
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
Angewandte Chemie (International Ed. in English)
Despite the high relevance of 1,3‐dienes, stereoselective methods to access tetrasubstituted conjugated dienes are still scarce. We here report an efficient and modular approach that provides access to multifunctional tetrasubstituted 1,3‐dienes
Autor:
Borja Pérez-Saavedra, Álvaro Velasco-Rubio, Eva Rivera-Chao, Jesús A. Varela, Carlos Saá, Martín Fañanás-Mastral
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
instname
Functionalized alicyclic amines are important building blocks for the synthesis of bioactive natural compounds and drugs. Existing methods of functionalization are typically limited to the synthesis of protected amines or the use of highly basic orga
Autor:
Jaime Mateos, Noelia Fuentes-Vara, Eva Rivera-Chao, Laura Fra, Andrea Chaves-Pouso, Nuria Vázquez-Galiñanes, Martín Fañanás-Mastral
Publikováno v:
Organometallics. 39:740-745
Cu/Pd-catalyzed alkyne allylboration with racemic allylic carbonates proceeds with total inversion of configuration. Preliminary studies show that this synergistic catalysis can be used to perform ...
Autor:
Yu Kawamata, Keun Ah Ryu, Gary Hermann, Alexander Sandahl, Julien Vantourout, Aleksandra Olow, La-Tonya Adams, Eva Rivera-Chao, Lee Roberts, Rob Oslund, Olugbeminiyi Fadeyi, phil baran
Target identification is a critical pillar within the drug discovery process that involves deconvoluting the protein target of a pharmacologically active small molecule ligand. While photoaffinity labeling strategies have become the benchmark for tar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b06e9180b77d091b52a2f118230574b3
https://doi.org/10.26434/chemrxiv-2022-s2m8f
https://doi.org/10.26434/chemrxiv-2022-s2m8f
Publikováno v:
Angewandte Chemie. 131:18398-18402
The first copper-catalyzed enantioselective allylboration of alkynes is reported. The method employs a multitasking chiral NHC-Cu catalyst and provides access to densely functionalized molecules from simple starting materials with excellent levels of
Autor:
Alexandre Genoux, Michał Biedrzycki, Eva Rivera-Chao, Estíbaliz Merino, Anthony Linden, Cristina Nevado
Publikováno v:
Angewandte Chemie (International ed. in English). 60(8)
A new family of cationic, bidentate (P^N)gold(III) fluoride complexes has been prepared and a detailed characterization of the gold‐fluoride bond has been carried out. Our results correlate with the observed reactivity of the fluoro ligand, which u
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
instname
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
A copper-catalyzed protoboration of borylated dendralenes is reported. The method employs an NHC–Cu catalyst and provides access to 1,4-addition products with excellent levels of chemo-, regio- and stereoselectivity. The resulting diene bis(boronat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23b1f9b80c4edecce39938ff8178290e
http://hdl.handle.net/10347/23373
http://hdl.handle.net/10347/23373
Publikováno v:
Synthesis. 50:3825-3832
Synergistic bimetallic catalysis has become a very efficient tool for the selective carboboration of unsaturated hydrocarbons. This synthetic approach is based on the use of a catalytically generated boron-substituted organocopper nucleophile in a cr
Publikováno v:
Angewandte Chemie International Edition. 57:9945-9949
An efficient method to access diversely substituted borylated dendralenes from simple and readily available materials is reported. This method is based on a multicomponent copper-catalyzed allylboration of alkynes with diboron and a 1,4-dibromo-2-but
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
instname
A Cu/Pd-catalyzed allylboration of alkynes with allyl carbonates and bis(pinacolato)diboron to afford borylated skipped dienes is reported. Synergistic Cu and Pd catalysis enables this protocol to work for a wide array of alkynes and allyl carbonates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce8b3bc95b4ea980a24628f15936b585
http://hdl.handle.net/10347/17015
http://hdl.handle.net/10347/17015