Fluorination-triggered tandem cyclization of styrene-type carboxylic acids to access 3-aryl isocoumarin derivatives under microwave irradiation-Reference-Cited by-同舟云学术

Fluorination-triggered tandem cyclization of styrene-type carboxylic acids to access 3-aryl isocoumarin derivatives under microwave irradiation

Published:2019 Issue:20 Volume:17 Page:5038-5046
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yuan Jinwei¹²³⁴^ORCID,Zeng Fanlin¹²³⁴,Mai Wenpeng⁵⁶⁷⁴,Yang Liangru¹²³⁴^ORCID,Xiao Yongmei¹²³⁴,Mao Pu¹²³⁴,Wei Donghui⁸⁹³⁴^ORCID

Affiliation:

1. School of Chemistry & Chemical Engineering

2. Henan University of Technology

3. Zhengzhou 450001

4. P. R. China

5. School of Material and Chemical Engineering

6. Henan Institute of Engineering

7. Zhengzhou 451191

8. College of Chemistry and Molecular Engineering

9. Zhengzhou University

Abstract

A practical synthetic route through a fluorination-triggered tandem cyclization of styrene-type carboxylic acids was developed to construct a variety of 4-fluoro-3-aryl-3,4-dihydroisocoumarins and 3-arylisocoumarins.

Funder

Science and Technology Department, Henan Province

Natural Science Foundation of Henan Province

Henan University of Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00509A

Reference122 articles.

1. The Structural Diversity of Phthalides from the Apiaceae

2. Isocoumarin Glucosides from the Scale Insect Fungus Torrubiella tenuis BCC 12732

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4. Synthesis and Antimicrobial Activities of Some Isocoumarin and Dihydroisocoumarin Derivatives

5. Polygonolide, an isocoumarin from Polygonum hydropiper possessing anti-inflammatory activity

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