Zobrazeno 1 - 10
of 239
pro vyhledávání: '"Robert A. Flowers"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1472-1479 (2013)
The synthesis of 2-tetralones through the cyclization of δ-aryl-β-dicarbonyl substrates by using CAN is described. Appropriately functionalized aromatic substrates undergo intramolecular cyclizations generating 2-tetralone derivatives in moderate t
Externí odkaz:
https://doaj.org/article/d067e7a28cd14ab782067a0ae2e1540f
Publikováno v:
Inorganic Chemistry. 62:5040-5045
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0a014fd86819d1834ea32f6527cf886
https://doi.org/10.1021/acs.inorgchem.3c00298
https://doi.org/10.1021/acs.inorgchem.3c00298
Publikováno v:
BMJ case reports. 14(11)
A gentleman in his 60s with end-stage kidney disease status post kidney transplantation on prednisone and tacrolimus presented with generalised weakness for 7 days, associated with altered mental status. Investigations revealed pancytopenia, acute ki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c0265635f360d8c3c4e2efa18a93477
https://pubmed.ncbi.nlm.nih.gov/34848413
https://pubmed.ncbi.nlm.nih.gov/34848413
Autor:
Nicholas G. Boekell, Robert A. Flowers
Publikováno v:
Chemical Reviews. 122:13447-13477
Coordination-induced bond weakening is a phenomenon wherein ligand X-H bond homolysis occurs in concert with the energetically favorable oxidation of a coordinating metal complex. The coupling of these two processes enables thermodynamically favorabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bdf82e81561b24d4f09bde0acce831f
https://doi.org/10.1021/acs.chemrev.2c00254
https://doi.org/10.1021/acs.chemrev.2c00254
Autor:
Humberto Saint-Martin, C. I. León-Pimentel, Robert A. Flowers, Alejandro Ramírez-Solís, Caroline O. Bartulovich, Nicholas G. Boekell
Publikováno v:
The Journal of Organic Chemistry. 87:1689-1697
Coordination-induced desolvation or ligand displacement by cosolvents and additives is a key feature responsible for the reactivity of Sm(II)-based reagent systems. High-affinity proton donor cosolvents such as water and glycols also demonstrate coor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96072290db661f78205f2bdc11d04edd
https://doi.org/10.1021/acs.joc.1c01771
https://doi.org/10.1021/acs.joc.1c01771
Publikováno v:
Tecnología y ciencias del agua, Vol 5, Iss 5, Pp 189-197 (2014)
Se realizó un estudio de Monte Carlo para determinar la validez del empleo de la prueba del error estándar de ajuste como criterio de selección en el análisis de frecuencias. Dicho estadístico se comparó con los estadísticos de prueba de Kolmo
Externí odkaz:
https://doaj.org/article/81db33a837bb4d1e8305723de3535e9f
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::288af4b0a27d217dd5d3fbcb0bd2c1b1
https://doi.org/10.7759/cureus.23906
https://doi.org/10.7759/cureus.23906
Autor:
Tobias Hilche, Robert A. Flowers, Niels R. Rietdijk, Daniel Slak, Andreas Gansäuer, Zhenhua Zhang, Ugochinyere N. Oloyede
Publikováno v:
Angewandte Chemie (International Ed. in English)
Irradiation of Cp2TiCl2 with green light leads to electronically excited [Cp2TiCl2]*. This complex constitutes an efficient photoredox catalyst for the reduction of epoxides and for 5‐exo cyclizations of suitably unsaturated epoxides. To the best o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bc596f6d965d57e6af7322d8e1e1ac7
https://doi.org/10.1002/ange.202001508
https://doi.org/10.1002/ange.202001508
Autor:
C. I. León-Pimentel, Caroline O. Bartulovich, Robert A. Flowers, Alejandro Ramírez-Solís, Nicholas G. Boekell, Humberto Saint-Martin
Publikováno v:
Dalton Transactions. 49:7897-7902
Proton donors are important components of many reactions mediated by samarium diiodide (SmI2). The addition of water to SmI2 creates a reagent system that enables the reduction of challenging substrates through proton-coupled electron-transfer (PCET)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::973c541021f33e3473949cbf98199b36
https://doi.org/10.1039/d0dt01221a
https://doi.org/10.1039/d0dt01221a