Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Estibaliz Coya"'
Autor:
Lide M. Rodriguez-Martinez, Estibaliz Coya, Yan Zhang, Heng Zhang, Xabier Judez, Wei Zhang, Itziar Aldalur, Michel Armand, Michal Piszcz, Uxue Oteo, Chunmei Li
Publikováno v:
Solid State Ionics. 318:95-101
Nanocomposite solid polymer electrolytes (NSPEs) comprising lithium salt based on two representative sulfonylimide anions (i.e., bis(fluorosulfonyl)imide ([N(SO2F)2]−, FSI−) and bis(trifluoromethanesulfonyl)imide ([N(SO2CF3)2]−, TFSI−)) have
Publikováno v:
European Journal of Organic Chemistry. 2017:2462-2468
Heteroaryllithium compounds, obtained by MesLi-mediated halogen/lithium exchange, undergo intramolecular addition onto acrylamide and acrylate moieties. Both electron-rich (thiophenyl) and electron-deficient (pyridinyl, quinolinyl) heteroaromatic hal
Autor:
Estibaliz Coya, Lide M. Rodriguez-Martinez, Zhibin Zhou, Heng Zhang, Chunmei Li, Michel Armand, Michal Piszcz, Teófilo Rojo
Publikováno v:
Chemical Society Reviews. 46:797-815
Electrochemical energy storage is one of the main societal challenges to humankind in this century. The performances of classical Li-ion batteries (LIBs) with non-aqueous liquid electrolytes have made great advances in the past two decades, but the i
Publikováno v:
European Journal of Organic Chemistry. 2016:2054-2063
The generation of quaternary and tertiary stereocentres at C-10 of the pyrroloisoquinoline skeleton through intramolecular Mizoroki–Heck reactions of 2-alkenyl-substituted pyrroles and pyrrolidines has been studied. The cyclizations proceeded in mo
Autor:
Eider Aranzamendi, Humberto González-Díaz, Nuria Sotomayor, C. Blázquez-Barbadillo, Esther Lete, Estibaliz Coya
Publikováno v:
RSC Advances. 6:38602-38610
Enantioselective intramolecular Heck–Heck cascade reactions have emerged as an excellent tool for the construction of polycyclic frameworks, such as lycorane alkaloids, xestoquinone and analogues. However, it is particularly difficult to rationaliz
Publikováno v:
Advanced Synthesis & Catalysis. 357:3206-3214
Publikováno v:
Advanced Synthesis & Catalysis. 356:1853-1865
Publikováno v:
Angewandte Chemie. 126:1454-1458
Eine einfache und flexible Methode fur die selektive Funktionalisierung aller Positionen des Imidazolrings durch regioselektive Arylierungen, Allylierungen, Acylierungen und Additionen an Aldehyde ist entwickelt worden. Ausgehend von dem leicht herzu
Publikováno v:
Angewandte Chemie International Edition. 53:1430-1434
A simple, flexible, and straightforward method for the functionalization of all the positions of the imidazole heterocycle through regioselective arylations, allylations, acylations, and additions to aldehydes is disclosed. Starting from the readily
Publikováno v:
ChemInform. 47