An Aminative Rearrangement of <i>O</i> ‐(Arenesulfonyl)hydroxylamines: Facile Access to <i>ortho</i> ‐Sulfonyl Anilines-Reference-Cited by-同舟云学术

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An Aminative Rearrangement of O ‐(Arenesulfonyl)hydroxylamines: Facile Access to ortho ‐Sulfonyl Anilines

Published:2022-07-07 Issue:33 Volume:61 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew Chem Int Ed

Author:

Morrill Charlotte¹,Gillespie James E.¹,Phipps Robert J.¹^ORCID

Affiliation:

1. Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK

Funder

Royal Society

Engineering and Physical Sciences Research Council

H2020 European Research Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202204025

Reference59 articles.

1. Sulfonation of Aniline

2.

3. Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry

4. Pharmaceutical and medicinal significance of sulfur (SVI)-Containing motifs for drug discovery: A critical review

5. From Antibacterial to Antitumour Agents: A Brief Review on The Chemical and Medicinal Aspects of Sulfonamides

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2. Iron‐catalyzed C‐7 Selective NH₂ Amination of Indoles;Angewandte Chemie International Edition;2024-09-02

3. Homogeneous Iron Catalyzed C−H Amination;ChemCatChem;2024-06-12

4. Site-selective arene C–H amination with iron-aminyl radical;Nature Catalysis;2024-04-01

5. Rearrangement of Arylsulfamates and Sulfates to Para-Sulfonyl Anilines and Phenols;Molecules;2024-03-23

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