Zobrazeno 1 - 10
of 123
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
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
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
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d95fc1ddf3f931b84524be0b32defb
https://doi.org/10.1016/j.jcat.2020.09.030
https://doi.org/10.1016/j.jcat.2020.09.030
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fa97dd0366dddfd22db3efb71942d51
https://doi.org/10.1039/c9qo01544b
https://doi.org/10.1039/c9qo01544b
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1368bdc63a70a3d3020d45eb8248e56
https://doi.org/10.1039/d0cy00118j
https://doi.org/10.1039/d0cy00118j
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f14314688e59f2e120615b7c9d8ff206
https://doi.org/10.1002/poc.4333
https://doi.org/10.1002/poc.4333
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::640c14ccc7dfaee5f3336b73901035af
https://pubmed.ncbi.nlm.nih.gov/35029264
https://pubmed.ncbi.nlm.nih.gov/35029264