Intramolecular nitration–aminocarbonylation of unactivated olefins: metal-free synthesis of γ-lactams-Reference-Cited by-同舟云学术

Intramolecular nitration–aminocarbonylation of unactivated olefins: metal-free synthesis of γ-lactams

Published:2019 Issue:54 Volume:55 Page:7796-7799
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Chen Dong¹²³⁴⁵,Ji Meishan¹²³⁴⁵,Zhu Chen¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province

2. College of Chemistry

3. Chemical Engineering and Materials Science

4. Soochow University

5. Suzhou

Abstract

A novel, metal-free synthesis of valuable γ-lactams through the radical-mediated nitration–aminocarbonylation of unactivated olefins is reported.

Funder

National Natural Science Foundation of China

Priority Academic Program Development of Jiangsu Higher Education Institutions

Soochow University

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/2019/CC/C9CC03736E

Reference92 articles.

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3. A short dipolar cycloaddition approach to γ-lactam alkaloids from cynometra hankei

4. Fleming−Tamao Oxidation and Masked Hydroxyl Functionality: Total Synthesis of (+)-Pramanicin and Structural Elucidation of the Antifungal Natural Product (−)-Pramanicin

5. A Concise, Asymmetric Synthesis of Tetramic Acid Derivatives

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