Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Diego J, Cárdenas"'
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d93a86f2ab34e87a955112286acbb8ee
https://doi.org/10.1002/ejoc.202200992
https://doi.org/10.1002/ejoc.202200992
Autor:
Naishka E. Caldero-Rodríguez, Enrique M. Arpa, Diego J. Cárdenas, Lara Martínez-Fernández, Steffen Jockusch, Sourav Kanti Seth, Inés Corral, Carlos E. Crespo-Hernández
Publikováno v:
The journal of physical chemistry. B. 126(24)
There is significant interest in developing suitable nucleoside analogs exhibiting high fluorescence and triplet yields to investigate the structure, dynamics, and binding properties of nucleic acids and promote selective photosensitized damage to DN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57d7df2650294c412e7202c63d0760ce
https://pubmed.ncbi.nlm.nih.gov/35679327
https://pubmed.ncbi.nlm.nih.gov/35679327
Publikováno v:
Chemical Communications. 57:2424-2427
The formation of catalytically active alkyl-Ni(i) complexes by comproportionation of diorgano-Ni(ii) precursors and Ni(0) species proceeds easily through triplet states by alkyl ligand exchange. The process involves inversion of the configuration at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75e48d9577acbfb444e35add2b8bc94c
https://doi.org/10.1039/d1cc00203a
https://doi.org/10.1039/d1cc00203a
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
A Pd-catalyzed C(sp3)–C(sp) bond formation for the direct functionalization of cyclobutenes with alkynes has been achieved, suggesting (DFT and control experiments) an unusual pathway of oxidative addition in tertiary iodoalkanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b89f093d82f6079814284ca97ffad25
https://hdl.handle.net/10486/703902
https://hdl.handle.net/10486/703902
Publikováno v:
Chemical communications (Cambridge, England). 57(68)
A synthesis of skipped 1,4-enynes through functionalization of the cyclobutene core with alkynes has been achieved, suggesting an unusual pathway of oxidative addition in tertiary iodoalkanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7bf7e7f52a3cb7e573d1a18b9477c8da
https://pubmed.ncbi.nlm.nih.gov/34342311
https://pubmed.ncbi.nlm.nih.gov/34342311
Publikováno v:
Advanced Synthesis & Catalysis. 362:146-151
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1648a0600461a6c78fd7fdcdfd16266
https://doi.org/10.1002/adsc.201901203
https://doi.org/10.1002/adsc.201901203
Publikováno v:
Chemistry – A European Journal. 25:14512-14516
We report a novel atom-economical Ni-catalyzed cyclization reaction of enynes with alkynylboronates. The reaction employs a non-expensive Ni salt, a phosphine-based ligand and easy-handling alkynylboronates as boron-carbon source. The reaction provid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e44047f7d97d2e001b8b99c1cab0f4
https://doi.org/10.1002/chem.201903405
https://doi.org/10.1002/chem.201903405
Autor:
Natalia Cabrera-Lobera, Michael L. Neidig, Diego J. Cárdenas, M. Teresa Quirós, Elena Buñuel, William W. Brennessel
Publikováno v:
Org Lett
We report a Ni-catalyzed diborylative cyclization of enynes that affords carbo- and heterocycles containing both alkyl- and alkenylboronates. The reaction is fully atom-economical, shows a broad scope, and employs a powerful and inexpensive catalytic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::370fdc772381578d945cb0c2eab1a1a0
https://doi.org/10.1021/acs.orglett.9b02485
https://doi.org/10.1021/acs.orglett.9b02485
Autor:
Noelia Fuentes, Diego J. Cárdenas, Luis Crovetto, Luis Lezama, Víctor Blanco, Juan M. Cuerva, Sandra Resa, Alba Millán, M. Luisa Marcos, Araceli G. Campaña, Duane Choquesillo-Lazarte
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
New N,N′-dimethyl-N,N′-bis(2-pyridylmethyl)-ethane-1,2-diamine derivatives bearing covalently linked OH and (CO)NH groups have been synthesized. The coordination of those pendant hydroxyl/amide groups to a Fe(ii) metal center is demonstrated both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b35bf7d4ae7714c54a23691369b6b70f
https://doi.org/10.1039/c8dt04689a
https://doi.org/10.1039/c8dt04689a
Autor:
Elena Buñuel, Rita Soler‐Yanes, Diego J. Cárdenas, Pablo Domingo-Legarda, M. Teresa Quirós‐López
Publikováno v:
European Journal of Organic Chemistry. 2018:4900-4904
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd88fdd8cd1d8947fb0e51e4336e974c
https://doi.org/10.1002/ejoc.201800849
https://doi.org/10.1002/ejoc.201800849