Direct C3-Selective Arylation of N-Unsubstituted Indoles with Aryl Chlorides, Triflates, and Nonaflates Using a Palladium–Dihydroxyterphenylphosphine Catalyst-Reference-Cited by-同舟云学术

Direct C3-Selective Arylation of N-Unsubstituted Indoles with Aryl Chlorides, Triflates, and Nonaflates Using a Palladium–Dihydroxyterphenylphosphine Catalyst

Published:2020-07-30 Issue:16 Volume:85 Page:10902-10912
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yamaguchi Miyuki¹,Hagiwara Ryoya¹,Gayama Kanami¹,Suzuki Kohei¹,Sato Yusuke¹,Konishi Hideyuki¹,Manabe Kei¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Research Foundation for Pharmaceutical Sciences, University of Shizuoka

Hamamatsu Foundation for Science and Technology Promotion

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c01494

Reference87 articles.

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

2. Biological importance of the indole nucleus in recent years: A comprehensive review

3. Biomedical Importance of Indoles

4. Indoles — A promising scaffold for drug development

5. Medicinal chemistry of indole derivatives: Current to future therapeutic prospectives

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