Preprint Review Version 1 Preserved in Portico This version is not peer-reviewed

Recent Applications of Pd-Catalyzed Suzuki-Miyaura and Buchwald-Hartwig Couplings in Pharmaceutical Process Chemistry.

Version 1 : Received: 1 November 2021 / Approved: 2 November 2021 / Online: 2 November 2021 (22:56:37 CET)

A peer-reviewed article of this Preprint also exists.

Takale, B.S.; Kong, F.-Y.; Thakore, R.R. Recent Applications of Pd-Catalyzed Suzuki–Miyaura and Buchwald–Hartwig Couplings in Pharmaceutical Process Chemistry. Organics 2022, 3, 1-21. Takale, B.S.; Kong, F.-Y.; Thakore, R.R. Recent Applications of Pd-Catalyzed Suzuki–Miyaura and Buchwald–Hartwig Couplings in Pharmaceutical Process Chemistry. Organics 2022, 3, 1-21.

Abstract

Cross coupling reactions have changed the way complex molecules are synthesized. In particular, Suzuki-Miyaura and Buchwald-Hartwig amination reactions have given opportunities to elegantly make pharmaceutical ingredients. Indeed, these reactions are forefront at both the stages of drug development, medicinal chemistry, and process chemistry. On one hand, these reactions have given medicinal chemists a tool to derivatize the core molecule to arrive at scaffold rapidly. On the other hand, these cross couplings have offered the process chemists a smart tool to synthesize the development candidates safely, quickly, and efficiently. Generally, the application of cross coupling reactions is broad, and this review will specifically focus on their real (pharma) world applications in large scale synthesis those appeared in last two years.

Keywords

Catalysis; Suzuki-Miyaura; Buchwald-Hartwig amination; Palladium; Pharmaceuticals, Process Chemistry

Subject

Chemistry and Materials Science, Organic Chemistry

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