Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Enrique Gómez-Bengoa"'
Publikováno v:
ACS Omega, Vol 6, Iss 36, Pp 23329-23346 (2021)
Externí odkaz:
https://doaj.org/article/891f7a7efd934c0bab4d3ec0b923631d
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 3059-3068 (2020)
The tandem gold(I)-catalyzed rearrangement/Nazarov reaction of enynyl acetates in which the double bond is embedded in a piperidine ring was computationally and experimentally studied. The theoretical calculations predict that the position of the pro
Externí odkaz:
https://doaj.org/article/ba817907da2c47e7bfc7b2d80fa07cc3
Autor:
Amparo Sanz-Marco, Samuel Martinez-Erro, Martin Pauze, Enrique Gómez-Bengoa, Belén Martín-Matute
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
Nucleophiles cannot be directly reacted with enolates due to polarity mismatching. Here, the authors developed an umpolung strategy for the selective synthesis of α-alkoxy carbonyl compounds by reaction of iridium enolates with nucleophilic alcohols
Externí odkaz:
https://doaj.org/article/4512de0e8120421faf358a40d8a268ba
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
C-H activation is a powerful method to form functionalised molecules, but is particularly challenging for unactivated sp3sites. Here the authors report a directing-group-free radical cascade process for converting vinyl azides and carboxylic acids to
Externí odkaz:
https://doaj.org/article/8554b14d36544c84abbb58a4cb4fdf3a
Autor:
Alejandro Torregrosa-Chinillach, Adrien Moragues, Haritz Pérez-Furundarena, Rafael Chinchilla, Enrique Gómez-Bengoa, Gabriela Guillena
Publikováno v:
Molecules, Vol 23, Iss 12, p 3299 (2018)
A primary amine-salicylamide derived from chiral trans-cyclohexane-1,2-diamine was used as an organocatalyst for the enantioselective conjugate addition of aldehydes, mainly α,α-disubstituted to N-substituted maleimides. The reaction was performed
Externí odkaz:
https://doaj.org/article/27901436b6bd40a8bb3ecd2ebc8bad6b
Autor:
José R. Martínez-Guillén, Jesús Flores-Ferrándiz, Cecilia Gómez, Enrique Gómez-Bengoa, Rafael Chinchilla
Publikováno v:
Molecules, Vol 23, Iss 1, p 141 (2018)
Primary amine-salicylamides derived from chiral trans-cyclohexane-1,2-diamines are used as organocatalysts for the enantioselective conjugate addition of α,α-disubstituted aldehydes to arylated and heteroarylated nitroalkenes. The reaction is perfo
Externí odkaz:
https://doaj.org/article/4f58190c2a9642c1b26dff6f223f9bd8
Autor:
Claudio Palomo, Mikel Oiarbide, Enrique Gómez-Bengoa, Antonia Mielgo, M. Concepción González-Rego, Jesús M. García, Alberto González, José M. Odriozola, Patricia Bañuelos, Anthony Linden
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 377-392 (2005)
Externí odkaz:
https://doaj.org/article/6e292cd9db7e49078479b5d6f6b32b16
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::048d9116b42a75753f892c374df2ca17
https://doi.org/10.1002/chem.202203286
https://doi.org/10.1002/chem.202203286
Autor:
Kananat Naksomboon, Enrique Gómez-Bengoa, Jaya Mehara, Jana Roithová, Edwin Otten, M. Ángeles Fernández-Ibáñez
Publikováno v:
Chemical Science, 14, 11, pp. 2943-2953
Chemical Science, 14, 2943-2953
Chemical Science, 14(11), 2943-2953. ROYAL SOC CHEMISTRY
Chemical Science, 14, 2943-2953
Chemical Science, 14(11), 2943-2953. ROYAL SOC CHEMISTRY
Pd-catalyzed C–H functionalization reactions of non-directed substrates have recently emerged as an attractive alternative to the use of directing groups. Key to the success of these transformations has been the discovery of new ligands capable of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::475b15b4b77b1537267ab09e8bab5af3
The irradiation of (Z)-4-arylidene-5(4H)-oxazolones 1a–1u with blue light (465 nm) in the presence of the photosensitizer [Ru(bpy)3](BF4)2 (2.5 mol%) and the Lewis acid BF3·OEt2 (2 equiv.) in deoxygenated methanol at room temperature affords the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ea15a044bae30cabe43a15ac313dad1
http://zaguan.unizar.es/record/126310
http://zaguan.unizar.es/record/126310