Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Francisco Garnes–Portolés"'
Autor:
Jorge Castellanos-Soriano, Francisco Garnes-Portolés, M. Consuelo Jiménez, Antonio Leyva-Pérez, Raúl Pérez-Ruiz
Publikováno v:
ACS Physical Chemistry Au, Vol 4, Iss 3, Pp 242-246 (2024)
Externí odkaz:
https://doaj.org/article/6679854b04ec4f82a3cf6d9e0f9c3598
Autor:
Francisco Garnes-Portolés, Sergio Sanz-Navarro, Jordi Ballesteros-Soberanas, Ana Collado-Pérez, Jorge Sánchez-Quesada, Estela Espinós-Ferri, Antonio Leyva-Pérez
Publikováno v:
The Journal of Organic Chemistry. 88:5962-5971
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::733127021a13f578a886449adfa25922
https://doi.org/10.1021/acs.joc.3c00314
https://doi.org/10.1021/acs.joc.3c00314
Publikováno v:
ChemSusChem.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::161af3ca428f7feef5774d70551951f3
https://doi.org/10.1002/cssc.202300200
https://doi.org/10.1002/cssc.202300200
Publikováno v:
Garnes-Portolés, F, Miguélez, R, Grayson, M N & Barrio, P 2022, ' Heteroatom-Tethered ω-Alkenylallylboronates: Stereoselective Synthesis of Heterocyclic Derived Alcohols ', Synthesis, vol. 54, no. 17, pp. 3817-3822 . https://doi.org/10.1055/s-0040-1719890
The synthesis of ω-alkenylallylboronates using a heteroatom tether to join both functional groups is described for the first time. Then, these unprecedented compounds were used in a tandem Brønsted acid catalyzed allylboration/ring-closing metathes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b1272fa4c07f6b2d4925e593f851f44
https://doi.org/10.1055/s-0040-1719890
https://doi.org/10.1055/s-0040-1719890
Publikováno v:
Synlett.
The industrial fragrance compound dehydromuscone was synthesized in five linear steps and 19% overall yield. The synthesis features a highly efficient nondiluted ring-closing metathesis macrocyclization reaction as a key step that proceeds at a 0.2 M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f3bc9330cc3f4e0d1f017332581c195
http://hdl.handle.net/10261/303976
http://hdl.handle.net/10261/303976
Autor:
Mercedes Boronat, Raúl Pérez-Ruiz, Jorge Castellanos-Soriano, Judit Oliver-Meseguer, M. Consuelo Jiménez, Francisco Garnes-Portolés, Juan C. Hernández-Garrido, Miguel López-Haro, Antonio Leyva-Pérez, Rossella Greco
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
instname
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
The palladium-catalysed cross-coupling reaction between alkenes and aryl halides (the Mizoroki–Heck reaction) is a powerful methodology to construct new carbon–carbon bonds. However, the success of this reaction is in part hampered by an extremel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e5c169d1fd2556e1c393646dc9b805c
https://doi.org/10.1038/s41929-021-00592-3
https://doi.org/10.1038/s41929-021-00592-3
Publikováno v:
Scopus
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
P. B. thanks the Spanish MINECO for a Ramón y Cajal contract (RyC-2016-20951). M.N.G. thanks the University of Bath for financial support.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d779e71623ab9157eacb22e16c1a6b02
http://hdl.handle.net/10651/61804
http://hdl.handle.net/10651/61804
Autor:
Carlos López-Cruz, Avelino Corma, Sergio Sanz-Navarro, Francisco Garnes-Portolés, Antonio Leyva-Pérez, Estela Espinós-Ferri
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
The industrially–viable aerobic α–alkylation of cyclic and acyclic ketones with allyl and alkyl alkenes in the presence of catalytic amounts of Mn, under homo– and heterogeneous conditions, is achieved here. The substitution of organic peroxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d448fc840a642aed50557678d8b1d197
http://hdl.handle.net/10261/268933
http://hdl.handle.net/10261/268933
Publikováno v:
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
[EN] The cyanosilylation of carbonyl compounds is a fundamental reaction in organic synthesis, to give cyanohydrins. Ketones are particularly reluctant to cyanosilane addition and require the action of a catalyst, and despite many soluble Bronsted an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3eaa1d7d352d0ded381291c03cd816a
http://hdl.handle.net/10251/182986
http://hdl.handle.net/10251/182986