PUBLICACIÓN

Clase invertida: ¿aprendizaje activo para la superación de ideas erróneas?

ACCEDER A LA PUBLICACIÓN: Dialnet

María José Arévalo Caballero

2017 II Jornadas de Innovación Docente en la Ingeniería: 26 de abril de 2017, Escuela Politécnica de Cáceres.

ISBN

9788469750209

AUTORES DE LA UEX

María José Arévalo Caballero

OTRAS PUBLICACIONES DE INTERÉS

Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Clase Invertida: ¿aprendizaje Activo Para La Superación De Ideas Erróneas?
¿usar Colillas Como Absorbentes Acústicos?
Clase Invertida: ¿aprendizaje Activo Para La Superación De Ideas Erróneas?
¿usar Colillas Como Absorbentes Acústicos?
Influence Of Acetic Acid And Calcium Hydroxide Treatments Of Rubber Waste On The Properties Of Rubberized Mortars
¿usar Colillas Como Absorbentes Acústicos?
Influence Of Acetic Acid And Calcium Hydroxide Treatments Of Rubber Waste On The Properties Of Rubberized Mortars
Green Chemical Synthesis And Click Reactions
Influence Of Acetic Acid And Calcium Hydroxide Treatments Of Rubber Waste On The Properties Of Rubberized Mortars
Green Chemical Synthesis And Click Reactions
Scope And Post-Transformations For The Borane-Isocyanide Multicomponent Reactions: Concise Access To Structurally Diverse Heterocyclic Compounds
Green Chemical Synthesis And Click Reactions
Scope And Post-Transformations For The Borane-Isocyanide Multicomponent Reactions: Concise Access To Structurally Diverse Heterocyclic Compounds
Multicomponent Reactions For De Novo Synthesis Of Bodipy Probes: In Vivo Imaging Of Phagocytic Macrophages
Scope And Post-Transformations For The Borane-Isocyanide Multicomponent Reactions: Concise Access To Structurally Diverse Heterocyclic Compounds
Multicomponent Reactions For De Novo Synthesis Of Bodipy Probes: In Vivo Imaging Of Phagocytic Macrophages
A Conjugate Addition/dipolar-Cycloaddition Cascade Sequence For The Synthesis Of (±)-Cylindricine C
Multicomponent Reactions For De Novo Synthesis Of Bodipy Probes: In Vivo Imaging Of Phagocytic Macrophages
A Conjugate Addition/dipolar-Cycloaddition Cascade Sequence For The Synthesis Of (±)-Cylindricine C
Multicomponent Access To Functionalized Mesoionic Structures Based On Tfaa Activation Of Isocyanides: Novel Domino Reactions
A Conjugate Addition/dipolar-Cycloaddition Cascade Sequence For The Synthesis Of (±)-Cylindricine C
Multicomponent Access To Functionalized Mesoionic Structures Based On Tfaa Activation Of Isocyanides: Novel Domino Reactions
Utilization Of A Michael Addition: Dipolar Cycloaddition Cascade For The Synthesis Of (±)-Cylindricine C
Multicomponent Access To Functionalized Mesoionic Structures Based On Tfaa Activation Of Isocyanides: Novel Domino Reactions
Utilization Of A Michael Addition: Dipolar Cycloaddition Cascade For The Synthesis Of (±)-Cylindricine C
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Utilization Of A Michael Addition: Dipolar Cycloaddition Cascade For The Synthesis Of (±)-Cylindricine C
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Enol Esters: Versatile Substrates For Mannich-Type Multicomponent Reactions
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Enol Esters: Versatile Substrates For Mannich-Type Multicomponent Reactions
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Enol Esters: Versatile Substrates For Mannich-Type Multicomponent Reactions
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Optically Active Sugar Thioamides From Δ-Gluconolactone
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Clase Invertida: ¿aprendizaje Activo Para La Superación De Ideas Erróneas?
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