Iron porphyrin catalysed light driven C–H bond amination and alkene aziridination with organic azides-Reference-Cited by-同舟云学术

Iron porphyrin catalysed light driven C–H bond amination and alkene aziridination with organic azides

Published:2020 Issue:18 Volume:11 Page:4680-4686
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Du Yi-Dan¹²³⁴⁵^ORCID,Zhou Cong-Ying¹²³⁴^ORCID,To Wai-Pong¹²³⁴^ORCID,Wang Hai-Xu¹²³⁴^ORCID,Che Chi-Ming¹²³⁴⁶^ORCID

Affiliation:

1. State Key Laboratory of Synthetic Chemistry

2. Department of Chemistry

3. The University of Hong Kong

4. China

5. Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis

6. HKU Shenzhen Institute of Research & Innovation

Abstract

An iron(iii) porphyrin catalysed sp³ C–H amination and alkene aziridination with broad substrate scope under mild conditions is conducted, with selectivity through the use of organic azides as the nitrogen source under blue LED light irradiation.

Funder

National Natural Science Foundation of China

Research Grants Council, University Grants Committee

Innovation and Technology Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/SC/D0SC00784F

Reference42 articles.

1. Transition metal-catalyzed iodine(iii)-mediated nitrene transfer reactions: efficient tools for challenging syntheses

2. Transition-Metal-Catalyzed C–N Bond Forming Reactions Using Organic Azides as the Nitrogen Source: A Journey for the Mild and Versatile C–H Amination

3. Asymmetric Nitrene Transfer Reactions: Sulfimidation, Aziridination and C-H Amination Using Azide Compounds as Nitrene Precursors

4. Metal-Catalyzed Nitrogen-Atom Transfer Methods for the Oxidation of Aliphatic C–H Bonds

5. Recent advances in transition metal-catalyzed N-atom transfer reactions of azides

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