Simplifying Nitration Chemistry with Bench-stable Organic Nitrating Reagents.

Patra, Subrata; Valsamidou, Vasiliki; Katayev, Dmitry (2024). Simplifying Nitration Chemistry with Bench-stable Organic Nitrating Reagents. CHIMIA, 78(1-2), pp. 32-39. Schweizerische Chemische Gesellschaft 10.2533/chimia.2024.32

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Nitro compounds play a crucial role in academia and industries, serving as building blocks for the synthesis of drugs, agrochemicals, and materials. Nitration, a fundamental process in organic synthesis, has undergone significant evolution since the 19th century. While electrophilic nitration dominates historically, recent decades have seen a focus on new reagents and their reactivity modes for achieving mild and robust synthesis of nitro compounds. Our group has a longstanding interest in developing cost-effective, readily available, recyclable nitrating reagents derived from organic scaffolds. These reagents serve as a controllable source of nitryl radical and nitronium ion species, enabling mild and practical nitration of hydrocarbons with exceptional functional group tolerance. This account details the development of nitrating reagents and their diverse applications in catalytic nitration across various classes of organic molecules.

Item Type:

Journal Article (Original Article)

Division/Institute:

08 Faculty of Science > Department of Chemistry, Biochemistry and Pharmaceutical Sciences (DCBP)

UniBE Contributor:

Patra, Subrata, Valsamidou, Vasiliki, Katayev, Dmitry

Subjects:

500 Science > 570 Life sciences; biology
500 Science > 540 Chemistry

ISSN:

0009-4293

Publisher:

Schweizerische Chemische Gesellschaft

Language:

English

Submitter:

Pubmed Import

Date Deposited:

04 Mar 2024 14:24

Last Modified:

05 Mar 2024 15:39

Publisher DOI:

10.2533/chimia.2024.32

PubMed ID:

38430061

Uncontrolled Keywords:

Nitration Nitronium ion Nitryl radicals Organic nitrating reagent Photoredox

BORIS DOI:

10.48350/193733

URI:

https://boris.unibe.ch/id/eprint/193733

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