Paul Rablen

Professor

Swarthmore College

United States

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Paul Rablen is a Professor at Swarthmore College in the United States. His research areas focus on electrophilic aromatic substitution, organic compound enthalpy formation, and catalysis techniques, as demonstrated in his recent articles. He has contributed significantly to the understanding of substituent effects and synthetic methodologies in organic chemistry.

Articles (13)

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2022

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2021

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2020

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2020

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2020

Collaborators (5)

Robert Pike

Professor

College of William and Mary

UNITED STATES

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Robert Barrows

Assistant Professor of Chemistry

Fairleigh Dickinson University - Florham Campus

UNITED STATES

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Christopher R. Graves

Swarthmore College

UNITED STATES

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William P. Malachowski

Bryn Mawr College

UNITED STATES

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Spencer Knapp

Rutgers University

UNITED STATES

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Paul Rablen

Research Interests

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Articles (13)

Typical Electron-Withdrawing Groups Are ortho, meta-Directors Rather than meta-Directors in Electrophilic Aromatic Substitution

Reversible O–H Bond Activation by Tripodal tris(Nitroxide) Aluminum and Gallium Complexes

Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy” Part V

Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy” Part VI

Ni-Catalyzed Enantioselective Intramolecular Mizoroki–Heck Reaction for the Synthesis of Phenanthridinone Derivatives

Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy” Part IV

The relative favorability of placing substituents ortho or para in the cationic intermediate for electrophilic aromatic substitution

A G4 approach to computing the Hammett substituent constants σp, σm, σ−, σ+, and σ+m

N-Oxazolidinoyl Diene Iron(0) Tricarbonyl Complexes: Preparation by Diastereoselective Complexation and Synthetic Applications

Stereoelectronic Features of a Complex Ketene Dimerization Reaction

Synthesis of Trialkylamines with Extreme Steric Hindrance and Their Decay by a Hofmann-like Elimination Reaction

A Procedure for Computing Hydrocarbon Strain Energies Using Computational Group Equivalents, with Application to 66 Molecules †

Increase in Strain Energy during Conversion of [4.4.4.5]Fenestrane to [4.4.4.4]Fenestrane: a Method for Estimating the Heats of Formation of Hydrocarbons and Their Derivatives from Ab Initio Energies

Collaborators (5)

Robert Pike

Robert Barrows

Christopher R. Graves

William P. Malachowski

Spencer Knapp

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