Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Asier Carral-Menoyo"'
Autor:
Verónica Ortiz-de-Elguea, Asier Carral-Menoyo, Lorena Simón-Vidal, Mikel Martinez-Nunes, Iratxe Barbolla, Marta G. Lete, Nuria Sotomayor, Esther Lete
Publikováno v:
ACS Omega, Vol 6, Iss 44, Pp 29483-29494 (2021)
Externí odkaz:
https://doaj.org/article/4f7124a2a6ff4aada79c0628dbe796ec
Publikováno v:
ACS Omega, Vol 5, Iss 39, Pp 24974-24993 (2020)
Externí odkaz:
https://doaj.org/article/8c30e2a5780c41969abc14efffadfdc6
Autor:
Asier Carral-Menoyo, Verónica Ortiz-de-Elguea, Mikel Martinez-Nunes, Nuria Sotomayor, Esther Lete
Publikováno v:
Marine Drugs, Vol 15, Iss 9, p 276 (2017)
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction of quinoline scaffolds, a privileged structure and prevalent motif in many natural and biologically active products, in particular in marine alkaloid
Externí odkaz:
https://doaj.org/article/aaa73e696d004906a8f6d9fc52dad09c
Autor:
Ashley Hogg, Matthew Wheatley, Pablo Domingo-Legarda, Asier Carral-Menoyo, Naomi Cottam, Igor Larrosa
Publikováno v:
Hogg, A, Wheatley, M, Domingo Legarda, P, Carral-Menoyo, A, Cottam, N & Larrosa, I 2022, ' Ruthenium-Catalyzed Mono-Selective C–H Methylation and d 3-Methylation of Arenes ', JACS Au . https://doi.org/10.1021/jacsau.2c00399
JACS Au
JACS Au
Site-selective installation of C–Me bonds remains a powerful and sought-after tool to alter the chemical and pharmacological properties of a molecule. Direct C–H functionalization provides an attractive means of achieving this transformation. Suc
Publikováno v:
Trends in Chemistry. 4:495-511
Autor:
Marta G. Lete, Nuria Sotomayor, Asier Carral-Menoyo, Iratxe Barbolla, Mikel Martinez-Nunes, Verónica Ortiz-de-Elguea, Esther Lete, Lorena Simón-Vidal
Publikováno v:
ACS Omega, Vol 6, Iss 44, Pp 29483-29494 (2021)
ACS Omega
Addi. Archivo Digital para la Docencia y la Investigación
instname
ACS Omega
Addi. Archivo Digital para la Docencia y la Investigación
instname
Highly substituted coumarins, privileged and versatile scaffolds for bioactive natural products and fluorescence imaging, are obtained via a Pd(II)-catalyzed direct C-H alkenylation reaction (Fujiwara-Moritani reaction), which has emerged as a powerf
Autor:
Alejandro Torregrosa-Chinillach, Asier Carral-Menoyo, Enrique Gómez-Bengoa, Rafael Chinchilla
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
A highly efficient enantioselective α-nitrogenation method of α,α-disubstituted aldehydes with azodicarboxylates promoted by a chiral carbamate-monoprotected cyclohexa-1,2-diamine as organocatalyst has been developed. The process was carried out w
Autor:
Dina Scarpi, Francesco Bagni, Cristina Faggi, Asier Carral-Menoyo, Enrique Gómez-Bengoa, Ernesto G. Occhiato
Publikováno v:
The Journal of organic chemistry. 87(9)
Six- and seven-membered ring-fused, functionalized cyclopentadienes can be obtained in moderate to excellent yields by a cascade process entailing the Au(I)-catalyzed propargyl Claisen rearrangement/Nazarov cyclization of propargyl vinyl ethers, the
Publikováno v:
ACS Omega, Vol 5, Iss 39, Pp 24974-24993 (2020)
ACS Omega
ACS Omega
The use of earth-abundant first-row transition metals, such as cobalt, in C-H activation reactions for the construction and functionalization of a wide variety of structures has become a central topic in synthetic chemistry over the last few years. I
Publikováno v:
Catalysis Science & Technology. 10:5345-5361
Quinoline and quinolone cores are present in a wide variety of pharmaceuticals, agrochemicals and materials as well as in ligands/catalysts in asymmetric synthesis. Transition metal catalysed based approaches have played a pivotal role in the develop