Synthesis of functionalized 3-aryl-3<i>H</i>-benzofuranone derivatives from aryl acetate <i>via</i> [3 + 2] annulation of 1,4-dihydroxy-2-naphthoic acid ester-Reference-Cited by-同舟云学术

Synthesis of functionalized 3-aryl-3H-benzofuranone derivatives from aryl acetate via [3 + 2] annulation of 1,4-dihydroxy-2-naphthoic acid ester

Published:2023 Issue:8 Volume:21 Page:1821-1826
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Huan¹,Zhou Yuxiang¹,Xie Ying¹^ORCID,Liu Yi¹,Li Yulong¹^ORCID,Zhang Hao²,Long Jilang³

Affiliation:

1. School of Chemistry and Environmental Engineering, Sichuan University of Science & Engineering, 180 Xueyuan Street, Huixing Lu, Zigong, Sichuan, 643000, China

2. College of Vanadium and Titanium, Panzhihua University, 10 Airport Lu, Panzhihua, Sichuan, 617000, China

3. College of Chemistry and Chemical Engineering, China West Normal University, 1 Shida Lu, Nanchong, Sichuan, 637002, China

Abstract

A new and efficient [3 + 2] cascade reaction has been developed for the synthesis of 3-aryl-3H-benzofuranone derivatives from aryl acetate via [3 + 2] annulation of 1,4-dihydroxy-2-naphthoic acid ester or 1,4-naphthoquinone.

Funder

Sichuan University of Science and Engineering

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D2OB02319A

Reference30 articles.

1. Electrolytic Macrocyclizations: Scalable Synthesis of a Diazonamide-Based Drug Development Candidate

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5. Gloriosaols A and B, two novel phenolics from Yucca gloriosa: structural characterization and configurational assignment by a combined NMR-quantum mechanical strategy

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