Simplifying Nitration Chemistry with Bench-stable Organic Nitrating Reagents.
Nitration
Nitronium ion
Nitryl radicals
Organic nitrating reagent
Photoredox
Journal
Chimia
ISSN: 0009-4293
Titre abrégé: Chimia (Aarau)
Pays: Switzerland
ID NLM: 0373152
Informations de publication
Date de publication:
28 Feb 2024
28 Feb 2024
Historique:
received:
30
11
2023
accepted:
01
12
2023
medline:
2
3
2024
pubmed:
2
3
2024
entrez:
2
3
2024
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 38430061
doi: 10.2533/chimia.2024.32
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
32-39Subventions
Organisme : Swiss National Science Foundation
ID : PCEFP2_186964
Pays : Switzerland
Informations de copyright
Copyright 2024 Subrata Patra, Vasiliki Valsamidou, Dmitry Katayev. License: This work is licensed under a Creative Commons Attribution 4.0 International License.