Area of research
Organic Chemistry · Inorganic Chemistry
Research interest
Research focused on Reagent and Aryl, with related work in Alkyl, Total synthesis, Carbene. Notable publications include 'Designing Pd–N-Heterocyclic Carbene Complexes for High Reactivity and Selectivity for Cross-Coupling Applications', 'Carbon–Heteroatom Coupling Using Pd-PEPPSI Complexes', and 'Pd‐PEPPSI‐IPent Cl : A Highly Effective Catalyst for the Selective Cross‐Coupling of Secondary Organozinc Reagents'.
Total Synthesis and Anti-Cancer Activity of All Known Communesin Alkaloids and Related Derivatives
Designing Pd–N-Heterocyclic Carbene Complexes for High Reactivity <i>and</i> Selectivity for Cross-Coupling Applications
Convergent and Biomimetic Enantioselective Total Synthesis of (−)-Communesin F
Pd‐<i>N</i>‐Heterocyclic Carbene Complexes in Cross‐Coupling Applications
The Selective Cross‐Coupling of Secondary Alkyl Zinc Reagents to Five‐Membered‐Ring Heterocycles Using Pd‐PEPPSI‐IHept<sup>Cl</sup>
The Selective Cross‐Coupling of Secondary Alkyl Zinc Reagents to Five‐Membered‐Ring Heterocycles Using Pd‐PEPPSI‐IHept<sup>Cl</sup>
ChemInform Abstract: The Selective Cross‐Coupling of Secondary Alkyl Zinc Reagents to Five‐Membered‐Ring Heterocycles Using Pd‐PEPPSI‐IHept<sup>Cl</sup>.
ChemInform Abstract: [(IPent)PdCl<sub>2</sub>(morpholine)]: A Readily Activated Precatalyst for Room‐Temperature, Additive‐Free Carbon‐Sulfur Coupling.
Frontispiz: The Selective Cross‐Coupling of Secondary Alkyl Zinc Reagents to Five‐Membered‐Ring Heterocycles Using Pd‐PEPPSI‐IHept<sup>Cl</sup>
Frontispiece: The Selective Cross‐Coupling of Secondary Alkyl Zinc Reagents to Five‐Membered‐Ring Heterocycles Using Pd‐PEPPSI‐IHept<sup>Cl</sup>
Room‐Temperature Amination of Deactivated Aniline and Aryl Halide Partners with Carbonate Base Using a Pd‐PEPPSI‐IPent<sup>Cl</sup>‐ <i>o</i>‐Picoline Catalyst
[(IPent)PdCl<sub>2</sub>(morpholine)]: A Readily Activated Precatalyst for Room‐Temperature, Additive‐Free Carbon–Sulfur Coupling
Room‐Temperature Amination of Deactivated Aniline and Aryl Halide Partners with Carbonate Base Using a Pd‐PEPPSI‐IPent<sup>Cl</sup>‐ <i>o</i>‐Picoline Catalyst
ChemInform Abstract: Room‐Temperature Amination of Deactivated Aniline and Aryl Halide Partners with Carbonate Base Using a Pd‐PEPPSI‐IPent<sup>Cl</sup>‐o‐Picoline Catalyst.
Carbon–Heteroatom Coupling Using Pd-PEPPSI Complexes
ChemInform Abstract: Pd‐PEPPSI‐IPent<sup>Cl</sup>: A Highly Effective Catalyst for the Selective Cross‐Coupling of Secondary Organozinc Reagents.
Pd‐PEPPSI‐IPent<sup>Cl</sup>: A Highly Effective Catalyst for the Selective Cross‐Coupling of Secondary Organozinc Reagents
Pd‐PEPPSI‐IPent<sup>Cl</sup>: A Highly Effective Catalyst for the Selective Cross‐Coupling of Secondary Organozinc Reagents