Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Adolfo Fernández-Figueiras"'
Publikováno v:
ACS Omega, Vol 7, Iss 8, Pp 6439-6448 (2022)
Externí odkaz:
https://doaj.org/article/9165df773db244a8910ed3a4fc8f1a01
Autor:
Miroslav Dangalov, Adolfo Fernández-Figueiras, Martin A. Ravutsov, Ekaterina Vakarelska, Maya K. Marinova, Nuno R. Candeias, Svilen P. Simeonov
Publikováno v:
ACS Catalysis. 13:1916-1925
A Ru-catalyzed isomerization of Achmatowicz derivatives that opens unexplored routes to diversify the biogenic furanic platform is reported. The mechanistic insights of this formally redox-neutral intramolecular process were studied computationally a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3432c72c2f3c94bad798654b9c621182
https://doi.org/10.1021/acscatal.2c04867
https://doi.org/10.1021/acscatal.2c04867
Publikováno v:
ACS Omega
The direct metal-catalyzed C-H functionalization of arenes has emerged as a powerful tool for streamlining the synthesis of complex molecular scaffolds. However, despite the different chemical environments, the energy values of all C-H bonds are with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c45bd557faaa433de91bd83ccc96c73b
https://pubmed.ncbi.nlm.nih.gov/35252639
https://pubmed.ncbi.nlm.nih.gov/35252639
Autor:
Paula Munín-Cruz, Fátima Lucio-Martínez, M. Teresa Pereira, Juan M. Ortigueira, José M. Vila, Paula Polo-Ces, Adolfo Fernández-Figueiras, Francisco Reigosa
Publikováno v:
ChemistryOpen
In the world of science, in particular the section concerning the field of chemistry, when the results encountered during the experiment do not meet our expectations, our shrewdness may play an important role to open up new unexplored fields that cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75b137a2acc6c01f6790a2db355a9900
http://europepmc.org/articles/PMC6173371
http://europepmc.org/articles/PMC6173371
Autor:
M. Teresa Pereira, Paula Munín-Cruz, Paula Polo-Ces, Francisco Reigosa, Adolfo Fernández-Figueiras, Harry Adams, Fátima Lucio-Martínez, José M. Vila
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 47(44)
Herein we report on the synthesis, characterization and the ensuing chemistry of iminophosphorane palladacycles. Treatment of Ph3P[double bond, length as m-dash]N-(2-OHC6H4), 1, with sodium tetrachloropalladate gives 2 with the ligand as terdentate [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da8a20f213426f286553a27be737bcc7
https://pubmed.ncbi.nlm.nih.gov/30357238
https://pubmed.ncbi.nlm.nih.gov/30357238
Autor:
Maria Pereira, Paula Munín, Adolfo Fernández-Figueiras, José M. Vila, Francisco Reigosa, Fátima Lucio, Paula Polo
Publikováno v:
Proceedings of The 21st International Electronic Conference on Synthetic Organic Chemistry.
The Suzuki-Miyaura cross coupling reaction is a very powerful tool for making of C–C bonds from organic halides and organoboron compounds [1]. This reaction, for which palladacycles have shown great catalytic activity [2] is widely employed in acad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97133c9ac17f6c76aad551d347fa4641
https://doi.org/10.3390/ecsoc-21-04773
https://doi.org/10.3390/ecsoc-21-04773
Autor:
José M. Vila, Paula Polo-Ces, Pablo Frieiro-Gomis, Maria Pereira, Adolfo Fernández-Figueiras, Francisco Reigosa-Chamorro
Publikováno v:
Proceedings of The 21st International Electronic Conference on Synthetic Organic Chemistry.
Thiosemicarbazone ligands are usually [N,S] donors rendering diverse coordination compounds and as [C,N,S] donors they give organometallic complexes. In this work, an unexpected isomerization of a C=N bond in a thiosemicarbazone is described. The lig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd4b748f628b25019d97cdb7b8f74d12
https://doi.org/10.3390/ecsoc-21-04775
https://doi.org/10.3390/ecsoc-21-04775
Autor:
Maria Pereira, Paula Munín, Adolfo Fernández-Figueiras, José M. Vila, Pablo Frieiro, Francisco Reigosa Chamorro, Fátima Lucio
Publikováno v:
Proceedings of The 21st International Electronic Conference on Synthetic Organic Chemistry.
– The aim of this work is the design, synthesis and characterization of a series of phenylboronic cyclometallated derivatives bearing different phosphines. Palladium cyclometallated compounds have proved to be useful as catalysts in cross coupling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e42db60b24800fdaf9cfa3934309f320
https://doi.org/10.3390/ecsoc-21-04744
https://doi.org/10.3390/ecsoc-21-04744
Autor:
Fátima Lucio, Paula Munín, Maria Pereira, Adolfo Fernández-Figueiras, Francisco Reigosa, José M. Vila, Juan M. Ortigueira
Publikováno v:
Proceedings of The 21st International Electronic Conference on Synthetic Organic Chemistry.
Transition metal complexes are useful in organic synthesis due to the capability of the metal to activate substrates [1-2]; in particular, cyclometallation reactions may lead to novel routes in organic synthesis. Thiosemicarbazones show a high coordi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad1a209bc10e9487b9a2a4013828c1e3
https://doi.org/10.3390/ecsoc-21-04745
https://doi.org/10.3390/ecsoc-21-04745
Autor:
José M. Vila, Adolfo Fernández-Figueiras, Maria Pereira, Francisco Reigosa, Paula Munín, Paula Polo, Fátima Lucio
Publikováno v:
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Universidad de Santiago de Compostela (USC)
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Iminophosphoranes are organic compounds of general composition R3P=NR and can be considered as nitrogen analogues to phophorus ylides. They can be obtained by the Staudinger[1] and Kirsanov[2] reactions. This compounds have multiple applications: the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4d9081a7522ece423ba6a27eccaad2f
https://doi.org/10.3390/ecsoc-20-a016
https://doi.org/10.3390/ecsoc-20-a016