INST. UNIV. INVEST.CENTRO INNOVACIÓN EN QUÍMICA Y MATERIALES AVANZADOS (CINQUIMA)
Institut
Universidad de Salamanca
Salamanca, EspañaPublications en collaboration avec des chercheurs de Universidad de Salamanca (10)
2022
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NHC-catalysed [3 + 2]-asymmetric annulation between pyrazolin-4,5-diones and enals: Synthesis of novel spirocyclic pyrazolone γ-butyrolactones and computational study of mechanism and stereoselectivity
Organic Chemistry Frontiers, Vol. 9, Núm. 2, pp. 420-427
2021
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A new MALDI-TOF approach for the quick sequence type identification of Legionella pneumophila
Journal of Microbiological Methods, Vol. 188
2019
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An Efficient Microkinetic Modeling Protocol: Start with only the Dominant Mechanisms, Adjust All Parameters, and Build the Complete Model Incrementally
ACS Catalysis, Vol. 9, Núm. 6, pp. 4804-4809
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Mimicking Halimane Synthases: Monitoring a Cascade of Cyclizations and Rearrangements from Epoxypolyprenes
Journal of Organic Chemistry, Vol. 84, Núm. 21, pp. 13764-13779
2018
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15-Hydroxygermacranolides as Sources of Structural Diversity: Synthesis of Sesquiterpene Lactones by Cyclization and Rearrangement Reactions. Experimental and DFT Study
Journal of Organic Chemistry, Vol. 83, Núm. 10, pp. 5480-5495
2017
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A DFT-Based Computational-Experimental Methodology for Synthetic Chemistry: Example of Application to the Catalytic Opening of Epoxides by Titanocene
Journal of Organic Chemistry, Vol. 82, Núm. 7, pp. 3760-3766
2016
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Cover Picture: Ti-Mediated Efficient Reductive Dehalogenation of Carbon–Halogen Bonds (Asian J. Org. Chem. 8/2016)
Asian Journal of Organic Chemistry
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Ti-Mediated Efficient Reductive Dehalogenation of Carbon–Halogen Bonds
Asian Journal of Organic Chemistry, Vol. 5, Núm. 8, pp. 991-1001
2015
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Homocoupling versus reduction of radicals: An experimental and theoretical study of Ti(iii)-mediated deoxygenation of activated alcohols
Organic and Biomolecular Chemistry, Vol. 13, Núm. 11, pp. 3462-3469
2013
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Structural diversity from the transannular cyclizations of natural germacrone and epoxy derivatives: A theoretical-experimental study
Chemistry - A European Journal, Vol. 19, Núm. 21, pp. 6598-6612