External-oxidant-free amino-benzoyloxylation of unactivated alkenes of unsaturated ketoximes with O-benzoylhydroxylamines-Reference-Cited by-同舟云学术

External-oxidant-free amino-benzoyloxylation of unactivated alkenes of unsaturated ketoximes with O-benzoylhydroxylamines

Published:2021 Issue:42 Volume:57 Page:5215-5218
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Chen Jiangfei¹²³⁴,Zhu Yan-Ping⁵⁶⁷⁸⁹^ORCID,Li Jin-Heng¹²³⁴⁵^ORCID,Wang Qiu-An¹²³⁴

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and Chemometrics

2. Hunan University

3. Changsha 410082

4. China

5. School of Pharmacy

6. Key Laboratory of Molecular Pharmacology and Drug Evaluation

7. Ministry of Education

8. Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong

9. Yantai University

Abstract

Radical-mediated aminobenzoyloxylation of alkenyl ketoximes using O-benzoylhydroxylamines as the benzoyloxyl radical precursors and internal oxidants is presented.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CC/D1CC01565F

Reference72 articles.

1. Synthesis of azaheterocycles from oxime derivatives

2. Generation and Application of Iminyl Radicals from Oxime Derivatives Enabled by Visible Light Photoredox Catalysis

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