Showing results (41-50 of 213) with videos related to
Sort By:
Pageof 22
Organic & Biomolecular Chemistry|August 21, 2014
Understanding the polar mechanism of the ene reaction. A DFT studyLuis R Domingo, Maria J Aurell, Patricia PérezOrganic & Biomolecular Chemistry|June 8, 2010
Quantitative characterization of group electrophilicity and nucleophilicity for intramolecular Diels-Alder reactionsJorge Soto-Delgado, Luis R Domingo, Renato ContrerasThe Journal of Organic Chemistry|August 19, 2024
Understanding the Electronic Effects of Lewis Acid Catalysts in Accelerating Polar Diels-Alder ReactionsLuis R Domingo, Mar Ríos-Gutiérrez, Patricia PérezMolecules (Basel, Switzerland)|November 21, 2019
A Molecular Electron Density Theory Study of the Synthesis of Spirobipyrazolines through the Domino Reaction of Nitrilimines with AllenoatesLuis R Domingo, Fatemeh Ghodsi, Mar Ríos-GutiérrezThe Journal of Organic Chemistry|January 29, 2013
Why do five-membered heterocyclic compounds sometimes not participate in polar Diels-Alder reactions?Luis R Domingo, Patricia Pérez, Daniela E OrtegaOrganic & Biomolecular Chemistry|April 25, 2012
Origin of the synchronicity in bond formation in polar Diels-Alder reactions: an ELF analysis of the reaction between cyclopentadiene and tetracyanoethyleneLuis R Domingo, Patricia Pérez, Jose A SáezMolecules (Basel, Switzerland)|June 14, 2016
Applications of the Conceptual Density Functional Theory Indices to Organic Chemistry ReactivityLuis R Domingo, Mar Ríos-Gutiérrez, Patricia PérezThe Journal of Organic Chemistry|February 6, 2026
Unveiling the Electronic Effects of the Lewis Acids in Nucleophilic Substitution Reactions from a Molecular Electron Density Theory PerspectiveLuis R Domingo, Maria José Aurell, Patricia PérezOrganic & Biomolecular Chemistry|December 18, 2019
A molecular electron density theory study of the enhanced reactivity of aza aromatic compounds participating in Diels-Alder reactionsLuis R Domingo, Mar Ríos-Gutiérrez, Patricia PérezRSC Advances|April 15, 2022
Understanding the different reactivity of (<i>Z</i>)- and (<i>E</i>)-β-nitrostyrenes in [3+2] cycloaddition reactions. An MEDT studyMar Ríos-Gutiérrez, Luis R Domingo, Radomir JasińskiPageof 22