Israel Fernández

Research interests

Publications

• Aromaticity: Quo Vadis

  Chemical Science · 2023 · 10.1039/d2sc04998h

• The Pauli Repulsion-Lowering Concept in Catalysis

  Accounts of Chemical Research · 2021 · 10.1021/acs.accounts.1c00016

• Metal–CO Bonding in Mononuclear Transition Metal Carbonyl Complexes

  JACS Au · 2021 · 10.1021/jacsau.1c00106

• How Lewis Acids Catalyze Diels–Alder Reactions

  Angewandte Chemie International Edition · 2020 · 10.1002/anie.201914582

• Homo and Hetero Molecular 3D Nanographenes Employing a Cyclooctatetraene Scaffold

  Journal of the American Chemical Society · 2019 · 10.1021/jacs.9b10203

• How Dihalogens Catalyze Michael Addition Reactions

  Angewandte Chemie International Edition · 2019 · 10.1002/anie.201903196

• Homo and Hetero Molecular 3D Nanographenes Employing a Cyclooctatetraene Scaffold

  Journal of the American Chemical Society · 2019 · 10.1021/jacs.9b10203

• How Dihalogens Catalyze Michael Addition Reactions

  Angewandte Chemie International Edition · 2019 · 10.1002/anie.201903196

• Homo and Hetero Molecular 3D Nanographenes Employing a Cyclooctatetraene Scaffold

  Journal of the American Chemical Society · 2019 · 10.1021/jacs.9b10203

• How Dihalogens Catalyze Michael Addition Reactions

  Angewandte Chemie International Edition · 2019 · 10.1002/anie.201903196

• Synthesis of a Helical Bilayer Nanographene

  Angewandte Chemie International Edition · 2018 · 10.1002/anie.201800798

• π-Extended Corannulene-Based Nanographenes: Selective Formation of Negative Curvature

  Journal of the American Chemical Society · 2018 · 10.1021/jacs.8b09992

• Aromaticity of metallabenzenes and related compounds

  Chemical Society Reviews · 2015 · 10.1039/c5cs00004a

• Aromaticity in transition structures

  Chemical Society Reviews · 2014 · 10.1039/c4cs00012a

• Allenes and computational chemistry: from bonding situations to reaction mechanisms

  Chemical Society Reviews · 2014 · 10.1039/c3cs60457h

• The activation strain model and molecular orbital theory: understanding and designing chemical reactions

  Chemical Society Reviews · 2014 · https://doi.org/10.1039/c4cs00055b

• Combined activation strain model and energy decomposition analysis methods: a new way to understand pericyclic reactions

  Physical Chemistry Chemical Physics · 2014 · 10.1039/c4cp00346b

• Combined activation strain model and energy decomposition analysis methods: a new way to understand pericyclic reactions

  Physical Chemistry Chemical Physics · 2014 · 10.1039/c4cp00346b

• Combined activation strain model and energy decomposition analysis methods: a new way to understand pericyclic reactions

  Physical Chemistry Chemical Physics · 2014 · 10.1039/c4cp00346b

• Why Do Cycloaddition Reactions Involving C60 Prefer [6,6] over [5,6] Bonds?

  Chemistry - A European Journal · 2013 · 10.1002/chem.201300648

• Why Do Cycloaddition Reactions Involving C60 Prefer [6,6] over [5,6] Bonds?

  Chemistry - A European Journal · 2013 · 10.1002/chem.201300648

• Why Do Cycloaddition Reactions Involving C60 Prefer [6,6] over [5,6] Bonds?

  Chemistry - A European Journal · 2013 · 10.1002/chem.201300648

• Description of Aromaticity in Porphyrinoids

  Journal of the American Chemical Society · 2012 · 10.1021/ja309434t

• Description of Aromaticity in Porphyrinoids

  Journal of the American Chemical Society · 2012 · 10.1021/ja309434t

• Description of Aromaticity in Porphyrinoids

  Journal of the American Chemical Society · 2012 · 10.1021/ja309434t

• Alder‐ene reaction: Aromaticity and activation‐strain analysis

  Journal of Computational Chemistry · 2011 · 10.1002/jcc.22877

• Alder‐ene reaction: Aromaticity and activation‐strain analysis

  Journal of Computational Chemistry · 2011 · 10.1002/jcc.22877

• Alder‐ene reaction: Aromaticity and activation‐strain analysis

  Journal of Computational Chemistry · 2011 · 10.1002/jcc.22877

• Rate-Determining Factors in Nucleophilic Aromatic Substitution Reactions

  The Journal of Organic Chemistry · 2010 · 10.1021/jo100195w

• Rate-Determining Factors in Nucleophilic Aromatic Substitution Reactions

  The Journal of Organic Chemistry · 2010 · 10.1021/jo100195w

• Rate-Determining Factors in Nucleophilic Aromatic Substitution Reactions

  The Journal of Organic Chemistry · 2010 · 10.1021/jo100195w

• Exocyclic Delocalization at the Expense of Aromaticity in 3,5-bis(π-Donor) Substituted Pyrazolium Ions and Corresponding Cyclic Bent Allenes

  Journal of the American Chemical Society · 2009 · 10.1021/ja903396e

• Exocyclic Delocalization at the Expense of Aromaticity in 3,5-bis(π-Donor) Substituted Pyrazolium Ions and Corresponding Cyclic Bent Allenes

  Journal of the American Chemical Society · 2009 · 10.1021/ja903396e

• Dyotropic Reactions: Mechanisms and Synthetic Applications

  Chemical Reviews · 2009 · 10.1021/cr900209c

• Exocyclic Delocalization at the Expense of Aromaticity in 3,5-bis(π-Donor) Substituted Pyrazolium Ions and Corresponding Cyclic Bent Allenes

  Journal of the American Chemical Society · 2009 · 10.1021/ja903396e

• Structural Evidence for Antiaromaticity in Free Boroles

  Angewandte Chemie International Edition · 2008 · 10.1002/anie.200704771

• Multimetallocenes. A Theoretical Study

  Organometallics · 2007 · 10.1021/om700477b

• Aromaticity in Metallabenzenes

  Chemistry - A European Journal · 2007 · 10.1002/chem.200601674

• Multimetallocenes. A Theoretical Study

  Organometallics · 2007 · 10.1021/om700477b

• Multimetallocenes. A Theoretical Study

  Organometallics · 2007 · 10.1021/om700477b

• Correlation between Hammett Substituent Constants and Directly Calculated π-Conjugation Strength

  The Journal of Organic Chemistry · 2006 · 10.1021/jo052012e

• Correlation between Hammett Substituent Constants and Directly Calculated π-Conjugation Strength

  The Journal of Organic Chemistry · 2006 · 10.1021/jo052012e

• Correlation between Hammett Substituent Constants and Directly Calculated π-Conjugation Strength

  The Journal of Organic Chemistry · 2006 · 10.1021/jo052012e

• Direct Estimate of the Strength of Conjugation and Hyperconjugation by the Energy Decomposition Analysis Method

  Chemistry - A European Journal · 2006 · 10.1002/chem.200501405

• Direct Estimate of the Strength of Conjugation and Hyperconjugation by the Energy Decomposition Analysis Method

  Chemistry - A European Journal · 2006 · 10.1002/chem.200501405

• Direct Estimate of the Strength of Conjugation and Hyperconjugation by the Energy Decomposition Analysis Method

  Chemistry - A European Journal · 2006 · 10.1002/chem.200501405

• Direct estimate of conjugation and aromaticity in cyclic compounds with the EDA method

  Faraday Discussions · 2006 · 10.1039/b606835a

Current projects

No projects listed.