Zobrazeno 1 - 10
of 135
pro vyhledávání: '"Ermitas Alcalde"'
Publikováno v:
ARKIVOC, Vol 2014, Iss 2, Pp 85-102 (2013)
Externí odkaz:
https://doaj.org/article/63dec426ffc74f84baf07629d2c81938
Publikováno v:
Molecules, Vol 17, Iss 4, Pp 4007-4027 (2012)
A broad and simple method permitted halide ions in quaternary heteroaromatic and ammonium salts to be exchanged for a variety of anions using an anion exchange resin (A− form) in non-aqueous media. The anion loading of the AER (OH− form) was exam
Externí odkaz:
https://doaj.org/article/4f2f472bced5473abf485e844e96af8b
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 1739-1744 (2011)
The synthesis of multifunctional indenes with at least two different functional groups has not yet been extensively explored. Among the plausible synthetic routes to 3,5-disubstituted indenes bearing two different functional groups, such as the [3-(a
Externí odkaz:
https://doaj.org/article/f266c0364e14458cb0d33d02f68e6ed4
Autor:
Santiago GarcÃÂa-Granda, Jordi Frigola, Rosa Cuberes, Carmen Alvarez-Rúa, Neus Mesquida, Ermitas Alcalde
Publikováno v:
Molecules, Vol 13, Iss 2, Pp 301-318 (2008)
The synthesis of a set of 1-aryl-2-aryl(3-pyridyl)ethanones 1-5 and thecorresponding ketoximes 6-9 is reported. Structural studies of oximes 6, 7 and 9 wereperformed in solution using 1H-NMR and in the solid state by X-ray crystallography,providing e
Externí odkaz:
https://doaj.org/article/8bae00336b4c442d9461358d6d118606
Publikováno v:
Beilstein Journal of Organic Chemistry
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 1739-1744 (2011)
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 1739-1744 (2011)
The synthesis of multifunctional indenes with at least two different functional groups has not yet been extensively explored. Among the plausible synthetic routes to 3,5-disubstituted indenes bearing two different functional groups, such as the [3-(a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ecd35736445ecdb9c0e038edc65ab6f
http://europepmc.org/articles/PMC3252879
http://europepmc.org/articles/PMC3252879
Publikováno v:
European Journal of Organic Chemistry. 2012:298-304
Faced with an extensive pool of imidazolium-based systems, the present study was based on selected examples of bis(imidazolium) models for anion recognition to broaden the applicability of counteranion exchange by using the anion-exchange resin (AER)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ec067e71035ac9615cc981e784a4afe
https://doi.org/10.1002/ejoc.201101355
https://doi.org/10.1002/ejoc.201101355
Autor:
Ermitas Alcalde, Enrique Hernández, Sara López-Pérez, Marta Pujol, Ramon Mercè, Jordi Frigola, Neus Mesquida, Jörg Holenz
Publikováno v:
Bioorganic & Medicinal Chemistry. 17:7387-7397
Further studies in quest of 5-HT(6) serotonin receptor ligands led to the design and synthesis of a few selected examples of N-(inden-5-yl)sulfonamides with a ring-constrained aminoethyl side chain at the indene 3-position, some of which exhibited a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fae12d45694feccf0847729966105743
https://doi.org/10.1016/j.bmc.2009.08.006
https://doi.org/10.1016/j.bmc.2009.08.006
Publikováno v:
Journal of Medicinal Chemistry. 52:675-687
Scaffold selection involving an indole-to-indene core change led to the discovery of a series of indenylsulfonamides that act as 5-HT6 serotonin receptor agonists. The variety of the targeted ligands and their synthetic complexity required multistep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d778f4b058f4dcc6090764b0661247e9
https://doi.org/10.1021/jm8009469
https://doi.org/10.1021/jm8009469
Autor:
Susana Ramos, Ermitas Alcalde, J. Fraser Stoddart, David J. Williams, Andrew J. P. White, Lluïsa Pérez-García
Publikováno v:
New J. Chem.. 33:300-317
The incorporation of proton ionizable moieties, such as 1H-1,2,4-triazole rings, within cyclophanes and π-donor/π-acceptor [2]catenanes is explored as a tool of inducing chemical switchability through either the inherent prototropic tautomerism or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6be24deb1667120b331fb0ea8735045a
https://doi.org/10.1039/b815355h
https://doi.org/10.1039/b815355h
Autor:
Neus Mesquida, Santiago García-Granda, Ermitas Alcalde, Carmen Alvarez-Rúa, Rosa Cuberes, Jordi Frigola
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Molecules
Volume 13
Issue 2
Pages 301-318
Molecules, Vol 13, Iss 2, Pp 301-318 (2008)
Universidad de Barcelona
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Molecules
Volume 13
Issue 2
Pages 301-318
Molecules, Vol 13, Iss 2, Pp 301-318 (2008)
The synthesis of a set of 1-aryl-2-aryl(3-pyridyl)ethanones 1-5 and thecorresponding ketoximes 6-9 is reported. Structural studies of oximes 6, 7 and 9 wereperformed in solution using 1H-NMR and in the solid state by X-ray crystallography,providing e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b649022ee08d1d0d1b344644593bb5cc
https://doi.org/10.3390/molecules13020301
https://doi.org/10.3390/molecules13020301