Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Matías I. Quindt"'
Publikováno v:
Photochemical and Photobiological Sciences, 21(5), 739-753. ROYAL SOC CHEMISTRY
Preparative and mechanistic studies on the photochemical reaction of a series of p-substituted benzanilides in polar and nonpolar solvents have been carried out. The aim of this work is mainly focused to show whether the reaction solvent and the elec
Autor:
Matías I. Quindt, Gabriel F. Gola, Cristian R. Rodriguez, Javier A. Ramirez, Sergio M. Bonesi
Publikováno v:
New Journal of Chemistry. 46:15504-15520
The photochemical reaction of sulfonate steroids in a sustainable environment was carried out successfully under steady-state conditions. Significant selectivity in photoproduct formation was also observed.
Publikováno v:
Photochemical & Photobiological Sciences. 21:625-644
In this study, we carried out preparative and mechanistic studies on the photochemical reaction of a series of 3-acylestrone derivatives in confined and sustainable micellar environment under steady-state conditions and the results were compared with
Autor:
José Luis Fonseca, María José Sosa, Gabriela Petroselli, Rosa Erra‐Balsells, Matías I. Quindt, Sergio M. Bonesi, Alexander Greer, Edyta M. Greer, Andrés H. Thomas, Mariana Vignoni
Publikováno v:
Photochemistry and photobiology.
Here, we provide mechanistic insight to the photocleavage of a compound in the folate family, namely pteroic acid. A bis-decyl chain derivative of pteroic acid was synthesized, structurally characterized, and photochemically investigated. We showed t
Publikováno v:
Photochemicalphotobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology. 21(5)
Preparative and mechanistic studies on the photochemical reaction of a series of p-substituted benzanilides in polar and nonpolar solvents have been carried out. The aim of this work is mainly focused to show whether the reaction solvent and the elec
Publikováno v:
Photochemicalphotobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology. 21(5)
In this study, we carried out preparative and mechanistic studies on the photochemical reaction of a series of 3-acylestrone derivatives in confined and sustainable micellar environment under steady-state conditions and the results were compared with
Publikováno v:
The Journal of Organic Chemistry. 84:7051-7065
Irradiation of a series of 3-acylestrones under a nitrogen atmosphere in cyclohexane, acetonitrile (MeCN), and methanol (MeOH) was investigated under steady-state conditions. The molecules underwent the photo-Fries rearrangement, with concomitant hom
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Direct irradiation of estrone aryl and methyl sulfonates in different organic solvents under nitrogen atmosphere was investigated under steady-state conditions. The estrone derivatives reacted efficiently through the photo-Fries rearrangement reactio