Hydroxamic Acids as Chemoselective (ortho -Amino)arylation Reagents via Sigmatropic Rearrangement-Reference-Cited by-同舟云学术

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Hydroxamic Acids as Chemoselective (ortho -Amino)arylation Reagents via Sigmatropic Rearrangement

Published:2017-08-02 Issue:36 Volume:56 Page:10938-10941
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Shaaban Saad¹,Tona Veronica¹,Peng Bo²,Maulide Nuno¹^ORCID

Affiliation:

1. Institute of Organic Chemistry; University of Vienna; Währinger Strasse 38 1090 Wien Austria

2. Department of Chemistry; Zhejiang Normal University; 688 Yingbin Road Jinhua 321004 China

Funder

FP7 Ideas: European Research Council

H2020 European Research Council

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference111 articles.

1. The Chemistry of Anilines

2. Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides

3. Recent advances in catalytic C–N bond formation: a comparison of cascade hydroaminomethylation and reductive amination reactions with the corresponding hydroamidomethylation and reductive amidation reactions

4. 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

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2. Modular Assembly of 2-Aminoaniline Derivatives by Merging Hydroxylamine-Passerini and Hetero-Cope Rearrangement;Organic Letters;2024-02-12

3. Synthesis of Indoles via Sigmatropic Rearrangements and Olefin Isomerization;Advanced Synthesis & Catalysis;2023-12-28

4. Regioselective umpolung para-C–H functionalization of arylhydroxylamines;Nature Synthesis;2023-04-27

5. Copper-catalyzed [1,3]-nitrogen rearrangement ofO-aryl ketoximesviaoxidative addition of N–O bond in inverse electron flow;Chemical Science;2023

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