Química Física y Analítica
Departamento
University of Lausanne
Lausana, SuizaPublicaciones en colaboración con investigadores/as de University of Lausanne (8)
2020
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Mineral and amino acid profiling of different hematopoietic populations from the mouse bone marrow
International Journal of Molecular Sciences, Vol. 21, Núm. 17, pp. 1-14
2019
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Systemic and central nervous system metabolic alterations in Alzheimer's disease
Alzheimer's Research and Therapy, Vol. 11, Núm. 1
2002
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Ab initio and experimental studies on the hetero-Diels-Alder and cheletropic additions of sulfur dioxide to (E)-1-methoxybutadiene: A mechanism involving three molecules of SO2
Journal of Organic Chemistry, Vol. 67, Núm. 6, pp. 1882-1889
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Cryo-negative staining reduces electron-beam sensitivity of vitrified biological particles
Journal of Structural Biology, Vol. 138, Núm. 3, pp. 216-226
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The hetero-Diels-Alder addition of sulfur dioxide to 1-fluorobuta-1,3-dienes: The sofa conformations preferred by 6-fluorosultines (6-fluoro-3,6-dihydro-1,2-oxathiin-2-oxides) enjoy enthalpic and conformational anomeric effects
Chemistry - A European Journal, Vol. 8, Núm. 6, pp. 1336-1355
2001
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The hetero-Diels-Alder addition of sulfur dioxide: Structure of the first crystalline sultine. Quantum calculations on the conformations of 6-fluoro-3,6-dihydro-1,2-oxathiine 2-oxides
Chemical Communications, Vol. 1, Núm. 13, pp. 1214-1215
2000
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17O NMR spectroscopy of sulfolenes (2,5-dihydrothiophene-1,1-dioxides) and sultines (3,6-dihydro-1,2-oxathiin-2-oxides) - Experiment and quantum calculations: Synthesis of 4,9-dioxo-1,2-oxathiacyclodecane-2-oxide, a new heterocycle
Chemistry - A European Journal, Vol. 6, Núm. 10, pp. 1858-1864
1998
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Competition between hetero-Diels-Alder and cheletropic addition of sulfur dioxide. Theoretical and experimental substituent effects on the relative stability of 3,6-dihydro-1,2-oxathiin-2-oxides (sultines) and 2,5- dihydrothiophene-1,1-dioxides (sulfolenes). Anomeric effects in sultine and 6-substituted derivatives
Journal of Organic Chemistry, Vol. 63, Núm. 25, pp. 9490-9499