3‐Arylcoumarin Scaffolds From 3‐Chlorocoumarin and Arylboronic Acids via Site‐Selective CCl Bond Activation With Palladium Complexes of NO Chelating Hydrazones

Author:

Shalini C.1ORCID,Akilesh M.1ORCID,Sathiyaraj G.1ORCID,Bhuvanesh N. S. P.2ORCID,Neethu K. S.1ORCID,Kaveri M. V.1ORCID,Dharmaraj N.1ORCID

Affiliation:

1. Inorganic and Nanomaterials Research Laboratory, Department of Chemistry Bharathiar University Coimbatore India

2. Department of Chemistry Texas A&M University College Station Texas USA

Abstract

ABSTRACTUsing 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)(PPh3)] by reacting the precursor complex [PdCl2(PPh3)2] with the hydrazone ligands HL1 or HL2. 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 CCl 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.

Publisher

Wiley

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