Literals
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- MARÍA GUADALUPE SILVERO ENRÍQUEZ
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- 12
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- MARÍA GUADALUPE
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- SILVERO ENRÍQUEZ
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- 7801437793
Typed Literals
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- A bioinspired look at the glucosinolate metabolic pathway. Structural insights into the reaction of benzyl isothiocyanate and d-glucosamine
- An in-depth look at the effect of Lewis acid catalysts on Diels-Alder cycloadditions in ionic liquids
- Atropisomeric carbohydrate imidazolidines: A novel class of nonbiaryl atropisomers
- Azodicarhoxamides vs. azodicarboxylates in reactions against thioisomünchnones: 1,3-dipolar cycloaddition or nucleophilic addition?
- Desulfurisation of oils using ionic liquids: Selection of cationic and anionic components to enhance extraction efficiency
- Determination of gels molecular structure by computational calculations
- Enhanced Diels-Alder reactions: on the role of mineral catalysts and microwave irradiation in ionic liquids as recyclable media
- Erratum: Synthesis of dihydrothiophenes by an amino-directed thioisomünchnone - Alkene cycloaddition reaction (European Journal of Organic Chemistry (2001) (2135-2144))
- Facile synthesis of 4,5-dihydro-1,3,4-thiadiazoles by 1,3-dipolar cycloaddition of thioisomünchnones
- Green heterogeneous catalysts for cleaner solvent-free production of acetates
- Ionic liquids: Opportunities for science and technology: Overview and highlights
- Non-biaryl atropisomers derived from carbohydrates. Part 3: Rotational isomerism of sterically hindered heteroaryl imidazolidine-2-ones and 2-thiones
- Non-biaryl atropisomers derived from carbohydrates. Part 1. Stereoselective synthesis of 1-aryl-5-hydroxyimidazolidine-2-thiones and their transformation into imidazoline-2-thiones
- Non-biaryl atropisomers derived from carbohydrates. Part 4: Absolute stereochemistry of carbohydrate-based imidazolidine-2-ones and 2-thiones with axial and central chirality
- Non-biaryl atropisomers derived from carbohydrates. Part 2. Atropisomeric behavior of monocyclic and bicyclic imidazolidine-2-ones and 2- thiones
- Reactions of 2-amino-2-thiazolines with isocyanates and isothiocyanates. Chemical and computational studies on the regioselectivity, adduct rearrangement, and mechanistic pathways
- Sonochemical cycloadditions in ionic liquids. Lessons from model cases involving common dienes and carbonyl dienophiles
- Synthesis and immobilisation of 2-aminoimidazole derivatives on the organosilanised surface of Ti6Al4V alloy.
- Synthesis of dihydrothiophenes by an amino-directed thioisomünchnone-alkene cycloaddition reaction
- Task-oriented use of ionic liquids: Efficient acetylation of alcohols and phenols
- The olive-tree leaves as a source of high-added value molecules: Oleuropein
- Theoretical study of the facial selectivity in Diels-Alder reactions of 4,4-disubstituted cyclohexadienones
- Theoretical study of the molecular structure for zirconium complexes
- Three- and four-membered rings from cycloadditions of 1,3-thiazolium-4-olates and aldehydes
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