Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jose A. Fernández‐Salas"'
Autor:
José Alemán, Jorge Humbrías-Martín, Roberto del Río-Rodríguez, Fernando Aguilar-Galindo, Sergio Díaz-Tendero, Jose A. Fernández-Salas
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-11 (2024)
Abstract Herein, an enantioselective desymmetrization of cyclic keto sulfonium salts through enantioselective deprotonation/ring opening process by anion-binding catalysis is presented. We report a squaramide/HCO3 - complex as catalytic active specie
Externí odkaz:
https://doaj.org/article/ab46aa7c04f14bf99cfd5175133987ad
Publikováno v:
Asymmetric Organocatalysis. :225-257
Autor:
Roberto del Río-Rodríguez, Matthew T. Westwood, Marina Sicignano, Martin Juhl, Jose A. Fernández-Salas, José Alemán, Andrew D. Smith
Publikováno v:
Chemical Communications. 58:7277-7280
Financial support was provided by the Spanish Government (RTI2018-095038-B-I00), “Comunidad de Madrid” for European Structural Funds (S2018/NMT-4367) and proyectos sinergicos I+D (Y2020/NMT-6469). J. A. F.-S. thanks the Spanish Government for a R
Autor:
Roberto del Río-Rodríguez, Lorena Fragoso-Jarillo, Alberto F. Garrido-Castro, M. Carmen Maestro, Jose A. Fernández-Salas, José Alemán
Herein, we report, a general, facile and environmentally friendly Minisci-type alkylation of N-heteroarenes under simple and straightforward electrochemical conditions using widely available alkyl halides as radical precursors. Primary, secondary and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72551f65305e2c73625ce2fb58f274be
https://doi.org/10.1039/d2sc01799g
https://doi.org/10.1039/d2sc01799g
Autor:
Roberto, Del Río-Rodríguez, Lorena, Fragoso-Jarillo, Alberto F, Garrido-Castro, M Carmen, Maestro, Jose A, Fernández-Salas, José, Alemán
Publikováno v:
Chemical science. 13(22)
Herein, we report, a general, facile and environmentally friendly Minisci-type alkylation of
Publikováno v:
Chemistry – A European Journal. 27
Autor:
Harry J. Shrives, José A. Fernández-Salas, Christin Hedtke, Alexander P. Pulis, David J. Procter
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
Benzothiophenes are common motifs in bioactive compounds, but selective functionalization at C3 is challenging. Here the authors report a method starting from benzothiophene S-oxides via an interrupted Pummerer reaction, giving access to a range of C
Externí odkaz:
https://doaj.org/article/96ecf75c80164e3692bef7fa44f24f7a