Area of research
Organic Chemistry · Inorganic Chemistry
Research interest
Research interests include Chemistry, Aryl, Negishi coupling, Catalysis, Reagent, and Alkyl.
Unexpected Deactivation of PdCl(cinnamyl)(NHC <sup>Cl</sup> ) Precatalysts Mediated by Alkylamines
Overcoming PAT Challenges in Automated Process Validation for Continuous Liquid–Gas Biphasic Processes
Experimental Evidence for Zerovalent Pd(NHC) as a Competent Catalyst in C–N Cross-Coupling (NHC = DiMeIHept<sup>Cl</sup>)
Doing More with Less, On Time and In Full: An Intelligent Multiattribute Process Optimization Platform
Sampling and Analysis in Flow: The Keys to Smarter, More Controllable, and Sustainable Fine‐Chemical Manufacturing
Sampling and Analysis in Flow: The Keys to Smarter, More Controllable, and Sustainable Fine‐Chemical Manufacturing
(DiMeIHept<sup>Cl</sup>)Pd: A Low-Load Catalyst for Solvent-Free (Melt) Amination
Obtaining Kinetics From Continuous Processes: Sampling Multiple Time Points Concurrently With a Single Valve Rotation
Structural Insights into the Inhibition of Undecaprenyl Pyrophosphate Synthase from Gram-Positive Bacteria
Intelligent Multidimensional Purity Analysis and Confirmation Tool for Multiple Attribute Analysis
The Synthesis of Warfarin Using a Reconfigurable‐Reactor Platform Integrated to a Multiple‐Variable Optimization Tool
Discovery of an antivirulence compound that reverses β-lactam resistance in MRSA
Murahashi Cross‐Coupling at −78 °C: A One‐Pot Procedure for Sequential C−C/C−C, C−C/C−N, and C−C/C−S Cross‐Coupling of Bromo‐Chloro‐Arenes
One‐Pot Sequential Kumada–Tamao–Corriu Couplings of (Hetero)Aryl Polyhalides in the Presence of Grignard‐Sensitive Functional Groups Using Pd‐PEPPSI‐IPent<sup>Cl</sup>
Rate and Computational Studies for Pd‐NHC‐Catalyzed Amination with Primary Alkylamines and Secondary Anilines: Rationalizing Selectivity for Monoarylation versus Diarylation with NHC Ligands
Sodium Butylated Hydroxytoluene (NaBHT) as a New and Efficient Hydride Source for Pd‐Catalysed Reduction Reactions
What Industrial Chemists Want—Are Academics Giving It to Them?
Designing Pd–N-Heterocyclic Carbene Complexes for High Reactivity <i>and</i> Selectivity for Cross-Coupling Applications
Pd‐PEPPSI‐IPent‐SiO<sub>2</sub>: A Supported Catalyst for Challenging Negishi Coupling Reactions in Flow
Process Analytical Tools for Flow Analysis: A Perspective
Pd‐PEPPSI‐IPent<sup>Cl</sup>: A Useful Catalyst for the Coupling of 2‐Aminopyridine Derivatives
Cross-Coupling of Primary Amides to Aryl and Heteroaryl Partners Using (DiMeIHept<sup>Cl</sup>)Pd Promoted by Trialkylboranes or B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>
A General Protocol for the Broad-Spectrum Cross-Coupling of Nonactivated Sterically Hindered 1° and 2° Amines
Pd‐PEPPSI‐IPent‐SiO<sub>2</sub>: A Supported Catalyst for Challenging Negishi Coupling Reactions in Flow
A Multiconfiguration Valve for Uninterrupted Sampling from Heterogeneous Slurries: An Application to Flow Chemistry
Continuous flow Negishi cross-couplings employing silica-supported Pd-PEPPSI–IPr precatalyst
Pd‐PEPPSI‐IHept<sup>Cl</sup>: A General‐Purpose, Highly Reactive Catalyst for the Selective Coupling of Secondary Alkyl Organozincs
Selective Cross-Coupling of (Hetero)aryl Halides with Ammonia To Produce Primary Arylamines using Pd-NHC Complexes
Handling Hazards Using Continuous Flow Chemistry: Synthesis of <i>N</i><sup>1</sup>-Aryl-[1,2,3]-triazoles from Anilines via Telescoped Three-Step Diazotization, Azidodediazotization, and [3 + 2] Dipolar Cycloaddition Processes
N‐Heteroarylation of Optically Pure α‐Amino Esters using the Pd‐PEPPSI‐IPent<sup>Cl</sup>‐<i>o</i>‐picoline Pre‐Catalyst