3‐Arylcoumarin Scaffolds From 3‐Chlorocoumarin and Arylboronic Acids via Site‐Selective CCl Bond Activation With Palladium Complexes of N<sup>∩</sup>O Chelating Hydrazones
ABSTRACT Using palladium hydrazone complex as a homogeneous catalyst for SMC, we synthesized a library of 15 variant 3‐arylcoumarins. In this context, we report a set of four coordinated palladium(II) hydrazone complexes 1 and 2 having the general formula [Pd(L)(Cl)(PPh 3 )] by reacting the precursor complex [PdCl 2 (PPh 3 ) 2 ] with the hydrazone ligands HL 1 or HL 2 . Single crystal XRD and conventional spectroscopic techniques were employed to characterize both complexes. From the catalytic application point of view, the new complexes 1 and 2 were tested as homogeneous catalysts towards the conversion of 3‐chlorocoumarins into 3‐arylcoumarins by activating the challenging CCl functionality. A minimal catalyst loading of complex 2 (0.01 mol%), afforded a series of 3‐arylcoumarins with a maximum of 92% yield and reusability up to five cycles. The present methodology is simple and easy to carry out at room temperature utilizing a green solvent (ethanol) in an open flask with a spectrum of aryl boronic acids.
Authors
- K.S. Neethu
- C. Shalini
- Kaveri M. Velusamy
- Nallasamy Dharmaraj (ORCID: https://orcid.org/0000-0001-7434-7072)
- G. Sathiyaraj
- Nattamai S. P. Bhuvanesh
- M. Akilesh
Institutions
- Bharathiar University (IN)
- Texas A&M University (US)
Publication Details
- Journal
- Applied Organometallic Chemistry
- Published
- 2024-08-20
- DOI
- https://doi.org/10.1002/aoc.7709
- Citations
- 2
- Primary Topic
- Synthesis and Biological Evaluation
- Type
- article
- Field-Weighted Citation Impact
- 0.50