Bimetallic copper/cobalt-cocatalyzed double aerobic phenol oxidation/cyclization toward π-extended benzofuro[2,3-b]indoles as electron donors for electroluminescence-Reference-Cited by-同舟云学术

Bimetallic copper/cobalt-cocatalyzed double aerobic phenol oxidation/cyclization toward π-extended benzofuro[2,3-b]indoles as electron donors for electroluminescence

Published:2021 Issue:14 Volume:23 Page:5031-5036
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Bashir Muhammad Adnan¹²³⁴⁵,Zhang Yulong¹²³⁴⁵,Yu Huaibin¹²³⁴⁵,Wang Bofei¹²³⁴⁵,Zhao Weining⁶⁷⁸⁹,Zhong Fangrui¹²³⁴⁵^ORCID

Affiliation:

1. Hubei Engineering Research Center for Biomaterials and Medical Protective Materials

2. Hubei Key Laboratory of Bioinorganic Chemistry & Materia Medica

3. School of Chemistry and Chemical Engineering

4. Huazhong University of Science and Technology (HUST)

5. Wuhan 430074

6. College of Pharmacy

7. Shenzhen Technology University

8. Shenzhen 518118

9. China

Abstract

π-Extended benzofuro[2,3-b]indoles were efficiently constructed from readily available p-hydroquinone esters and indoles via aerobic oxidation.

Funder

Hubei Technological Innovation Special Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/GC/D1GC01658J

Reference46 articles.

1. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

2. Synthesis and molecular properties of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles for organic electronics obtained by a consecutive twofold Suzuki and twofold Cadogan reaction

3. Eight‐Step Total Synthesis of Phalarine by Bioinspired Oxidative Coupling of Indole and Phenol

4. Direct Oxidative Coupling ofN-Acetyl Indoles and Phenols for the Synthesis of Benzofuroindolines Related to Phalarine

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

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