Issue 17, 2020

Synthesis of phenanthridines by I2-mediated sp3 C–H amination

Abstract

An I2-mediated synthesis of phenanthridines via intramolecular sp3 C–H amination of readily accessible aniline precursors is reported. The present synthetic process is straightforward and applicable to a broad variety of unprotected aniline substrates, and provides facile and efficient access to phenanthridine derivatives. This C–H amination protocol does not use transition metals, is operationally simple, and can be achieved on a gram scale.

Graphical abstract: Synthesis of phenanthridines by I2-mediated sp3 C–H amination

Supplementary files

Article information

Article type
Paper
Submitted
27 Feb 2020
Accepted
09 Apr 2020
First published
09 Apr 2020

Org. Biomol. Chem., 2020,18, 3312-3323

Synthesis of phenanthridines by I2-mediated sp3 C–H amination

B. Fang, J. Hou, J. Tian, W. Yu and J. Chang, Org. Biomol. Chem., 2020, 18, 3312 DOI: 10.1039/D0OB00433B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements