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Streamlining the synthesis of amides using Nickel-based nanocatalysts

Chemistry

Streamlining the synthesis of amides using Nickel-based nanocatalysts

J. Gao, R. Ma, et al.

Explore a groundbreaking method for amide synthesis that leverages the reductive amidation of esters with nitro compounds without additives. This innovative approach, developed by Jie Gao, Rui Ma, Fairoosa Poovan, and others, showcases the selective preparation of diverse amides, making it a game-changer for drug synthesis and biocompound modifications.

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Playback language: English
Abstract
This paper presents a novel, robust methodology for amide synthesis via the reductive amidation of esters with nitro compounds under additive-free conditions. A heterogeneous nickel-based catalyst enables the selective preparation of a wide range of amides with diverse functional groups, showcasing step-economy compared to traditional methods. The synthesis of drugs and late-stage modifications of bioactive compounds highlight the protocol's value. Control experiments, material characterizations, and DFT computations suggest that metallic nickel and low-valent Ti species are crucial for this direct amide synthesis.
Publisher
Nature Communications
Published On
Aug 17, 2023
Authors
Jie Gao, Rui Ma, Fairoosa Poovan, Lan Zhang, Hanan Atia, Narayana V. Kalevaru, Wenjing Sun, Sebastian Wohlrab, Denis A. Chusov, Ning Wang, Rajenahally V. Jagadeesh, Matthias Beller
Tags
amide synthesis
reductive amidation
nickel catalyst
step-economy
drug synthesis
nitro compounds
bioactive compounds
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