Tandem radical cyclization of N-methacryloyl benzamides with CBr4 to construct brominated isoquinolinediones-Reference-Cited by-同舟云学术

Tandem radical cyclization of N-methacryloyl benzamides with CBr4 to construct brominated isoquinolinediones

Published:2018 Issue:41 Volume:16 Page:7748-7752
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Huang Songhai¹²³⁴⁵,Niu Pengfei¹²³⁴⁵,Su Yingpeng¹²³⁴⁵^ORCID,Hu Dongcheng¹²³⁴⁵,Huo Congde¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Eco-Environment-Related Polymer Materials Ministry of Education

2. College of Chemistry and Chemical Engineering

3. Northwest Normal University

4. Lanzhou

5. China

Abstract

Cumene promoted auto-oxidation involved tandem radical cyclization of N-methacryloyl benzamides using CBr₄ as the bromine source to construct brominated isoquinolinediones is described.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01964A

Reference45 articles.

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2. Magnesium Chelating 2-Hydroxyisoquinoline-1,3(2H,4H)-diones, as Inhibitors of HIV-1 Integrase and/or the HIV-1 Reverse Transcriptase Ribonuclease H Domain: Discovery of a Novel Selective Inhibitor of the Ribonuclease H Function

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4. 4-(Phenylaminomethylene)isoquinoline-1,3(2H,4H)-diones as Potent and Selective Inhibitors of the Cyclin-Dependent Kinase 4 (CDK4)

5. Aerobic oxidative cyclization of benzamides via meta-selective C–H tert-alkylation: rapid entry to 7-alkylated isoquinolinediones

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