A Reusable Palladium Catalyst for Allylic Arylation of Baylis‐Hillman Adducts via Heck Arylation‐Isomerization Cascade Under Solvent‐Free Conditions

ABSTRACT A facile and sustainable intermolecular Heck arylation/isomerization of Baylis–Hillman adducts with iodobenzene, leading toward the synthesis of α ‐benzyl‐ β ‐keto esters using a novel heterogeneous palladium catalyst under milder conditions, is demonstrated. This polymer‐supported palladium catalyst ( mPAN‐Pd ) was tailored by immobilizing PdCl 2 onto post‐functionalized polyacrylonitrile ( mPAN ). The key feature of this protocol involves simple catalyst preparation, rapid reactions with excellent conversion up to 96% yield under solvent/ligand‐free and open‐air conditions. Above all, the catalyst offered easy recyclability by simple filtration and exhibited excellent catalytic activity and stability up to five repeated reaction cycles.

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Journal
ChemistrySelect
Published
2026-05-01
DOI
https://doi.org/10.1002/slct.73396
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

A Reusable Palladium Catalyst for Allylic Arylation of Baylis‐Hillman Adducts via Heck Arylation‐Isomerization Cascade Under Solvent‐Free Conditions

Chennattuparambil Roy Nathaniel, Pambingal Rajan Sruthi, Ayisha Fathima, Saithalavi Anas et al.
ChemistrySelect
Catalytic C–H Functionalization Methods
article

A Reusable Palladium Catalyst for Allylic Arylation of Baylis‐Hillman Adducts via Heck Arylation‐Isomerization Cascade Under Solvent‐Free Conditions

Chennattuparambil Roy Nathaniel, Pambingal Rajan Sruthi, Ayisha Fathima, Saithalavi Anas, Manchery Shimi, Vincent Joseph, Ananthu Sudheesh
article en

Abstract

ABSTRACT A facile and sustainable intermolecular Heck arylation/isomerization of Baylis–Hillman adducts with iodobenzene, leading toward the synthesis of α ‐benzyl‐ β ‐keto esters using a novel heterogeneous palladium catalyst under milder conditions, is demonstrated. This polymer‐supported palladium catalyst ( mPAN‐Pd ) was tailored by immobilizing PdCl 2 onto post‐functionalized polyacrylonitrile ( mPAN ). The key feature of this protocol involves simple catalyst preparation, rapid reactions with excellent conversion up to 96% yield under solvent/ligand‐free and open‐air conditions. Above all, the catalyst offered easy recyclability by simple filtration and exhibited excellent catalytic activity and stability up to five repeated reaction cycles.

ChemistrySelectVol. 11(17)
Mahatma Gandhi University (IN)
Council of Scientific and Industrial Research, India
Responsible consumption and production
Openalex Percentile: Top 10%
Catalytic C–H Functionalization Methods
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