Zobrazeno 1 - 10
of 179
pro vyhledávání: '"Olalla Nieto Faza"'
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 16976-16988 (2018)
Externí odkaz:
https://doaj.org/article/bfa1e0581cb84e168ad1671012d0fedc
Publikováno v:
ACS Omega, Vol 3, Iss 6, Pp 7019-7026 (2018)
Externí odkaz:
https://doaj.org/article/d42823b586c64bbd9ff14cacd2010ef4
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
Gold is currently one of the most used metals in organometallic catalysis. The ability of gold to activate unsaturated groups in different modes, together with its tolerance to a wide range of functional groups and reaction conditions, turns gold-bas
Externí odkaz:
https://doaj.org/article/b0e944c91011428bbac8b7b808856bba
In this work, we use density functional theory to unravel the mechanism of the nitrobenzene to aniline reduction, catalyzed by dioxomolybdenum (VI) dichloride. The use of pinacol as an oxoaccepting reagent and the production of only acetone and water
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::056bbb818a811972b39d2624f105bee0
https://doi.org/10.26434/chemrxiv-2023-cgtdn
https://doi.org/10.26434/chemrxiv-2023-cgtdn
Publikováno v:
Molecules, Vol 24, Iss 20, p 3810 (2019)
The magnitude of intramolecular basis set superposition error (BSSE) is revealed via computing systematic trends in molecular properties. This type of error is largely neglected in the study of the chemical properties of small molecules and it has hi
Externí odkaz:
https://doaj.org/article/9170fb914d824239ba9b3ceccc5f439d
Autor:
Olalla Nieto Faza, Marta Castiñeira Reis, Nenad Janković, Carlos Silva López, Marta Marin-Luna
Publikováno v:
Journal of Catalysis, 392, 159-164. ACADEMIC PRESS INC ELSEVIER SCIENCE
In the last decade substantial efforts were devoted towards the exploitation of the Au(I) as a promising tool to promote C[sbnd]C bond formation reactions via the activation of unsaturations. Among these efforts, Au(I)/Au(III) cross couplings mediate
Publikováno v:
Organic Chemistry Frontiers. 7:997-1005
Indole is a very common structural motif in alkaloids, and a number of them feature remarkable bioactive properties. Due to its relevant role in medicinal chemistry and the pharma-industry, many methods for indole synthesis have been developed, but o
Autor:
Béatrice Jacques, João Henrique Zimnoch dos Santos, Carlos Silva López, Yuri C. A. Sokolovicz, David Specklin, Henri Stephan Schrekker, Olalla Nieto Faza, Samuel Dagorne
Publikováno v:
Catalysis Science & Technology
Catalysis Science & Technology, Royal Society of Chemistry, 2020, 10 (8), pp.2407-2414. ⟨10.1039/d0cy00118j⟩
Catalysis Science & Technology, Royal Society of Chemistry, 2020, 10 (8), pp.2407-2414. ⟨10.1039/d0cy00118j⟩
International audience; The present study details the use of the acetate anion, an inexpensive and robust anion, as a CO2 hydroboration catalyst for the selective formation, in most cases, of methanol-equivalent borane products. Thus, upon heating (9
Autor:
Ioannis Stylianakis, Iraklis Litinas, Olalla Nieto Faza, Antonios Kolocouris, Carlos Silva López
Publikováno v:
Journal of Physical Organic Chemistry. 35
Indole is a very common structural motif in alkaloids with a remarkable history in pharma industry. In the continuous search for more direct and efficient access to these valuable structures, a new and rather elegant approach was found by Jin and cow
Publikováno v:
Organicbiomolecular chemistry. 20(5)
A combined computational/experimental approach has revealed key mechanistic aspects in a recently reported dyotropic expansion of hydrindanes into decalins. While computer simulations had already anticipated the need for acid catalysis for making thi