Palladium-Catalyzed Acylation Strategies and Their Applications Towards Biologically Relevant Products

Abstract

Ketones are fundamental synthons in organic synthesis due to their wide range of applications, which include natural products, pharmaceuticals, dyes, fragrances, agrochemicals, and electronic materials. In recent years, direct acylation strategies based on commercially available benchtop aryl halides and aldehydes (alkyl/aryl) have been the prime focus for the construction of alkyl-aryl/aryl-aryl ketones using palladium catalysis under eco-friendly reaction conditions. In this account, we present conceptually developed palladium-catalyzed direct acylation strategies for achieving various carbo- and heterocycles such as ketones, 2-quinolinones, phthalazines, phthalazinones, benzoxazinones, anthraquinones, indenones, and 1,3-dihydroisobenzofurans. Significantly, these direct acylation strategies have been extended to synthesize the natural product neo-lignan and biologically significant molecules such as an n-butylphthalide antiplatelet drug, pitofenone, fenofibrate, a HBV inhibitor, and a PDE-4 inhibitor. This Account will be of interest to synthetic organic chemists wishing to prepare pharmaceutical molecules and natural products.

1 Introduction

2 Discussion

2.1 Palladium-Catalyzed Environmentally Compassionate Acylation

2.2 Palladium-Catalyzed Acylations Followed by Intramolecular Aldol Condensation to Afford Indenones

2.3 Acylation of Iodo-acetanilides/Iodo-phenyl Acetates: Sequential One-Pot Syntheses of 2-Quinolinones

2.4 A One-Pot Diversified Synthesis of Phthalazines, Phthalazinones, and Benzoxazinones

2.5 Palladium-Catalyzed Direct Acylation: A One-Pot Relay Synthesis of Anthraquinones

2.6 Palladium-Catalyzed Direct Oxidative Coupling of Primary Alcohols with Iodoarenes Leading to Ketones: Application to the Synthesis of Benzofuranones and Indenones

3 Conclusion

Key words

palladium catalysis - acylation - n-butylphthalide - fenofibrate - HBV inhibitor - neo-lignan - pitofenone - PDE-4 inhibitor

Publikationsverlauf

Eingereicht: 23. März 2023

Angenommen nach Revision: 03. Mai 2023

Artikel online veröffentlicht:
05. Juni 2023

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