Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Eva Rivera"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a4a12df1b0e357e5dbf6a7c5f88f2a4
https://doi.org/10.1002/ange.202104741
https://doi.org/10.1002/ange.202104741
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e20581edfe0066f2ae072d6f4bc510e
https://pubmed.ncbi.nlm.nih.gov/36001853
https://pubmed.ncbi.nlm.nih.gov/36001853
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 ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb15ea1cd3a95691cdbde825ecefdf61
https://doi.org/10.1021/acs.organomet.0c00010
https://doi.org/10.1021/acs.organomet.0c00010
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::099165d858c7703f21d70c86e1bbe20d
https://doi.org/10.1002/ange.201910707
https://doi.org/10.1002/ange.201910707
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bab1f6fb934a3208747d93ad238e161
https://pubmed.ncbi.nlm.nih.gov/33015997
https://pubmed.ncbi.nlm.nih.gov/33015997
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e759a63f52eac4b6c33d6c06073e531
https://doi.org/10.1055/s-0037-1610434
https://doi.org/10.1055/s-0037-1610434
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8111c6deb78759347f02a7f98364c139
https://doi.org/10.1002/anie.201806334
https://doi.org/10.1002/anie.201806334