Issue 42, 2019

PIDA-mediated α-C–H functionalization of enaminones: the synthesis of thiocyano enaminones and chromones in water

Abstract

Herein, an efficient, metal-free process for the α-C–H thiocyanation of enaminones was developed using PhI(OAc)2 as an oxidant at room temperature in an aqueous medium. Various SCN-containing enaminones and chromones with broad functional groups were synthesized in moderate to good yields in the presence of KSCN. In addition, 3-selenocyanochromone was synthesized using this fast, green, metal-free approach.

Graphical abstract: PIDA-mediated α-C–H functionalization of enaminones: the synthesis of thiocyano enaminones and chromones in water

Supplementary files

Article information

Article type
Letter
Submitted
05 Sep 2019
Accepted
01 Oct 2019
First published
01 Oct 2019

New J. Chem., 2019,43, 16441-16444

PIDA-mediated α-C–H functionalization of enaminones: the synthesis of thiocyano enaminones and chromones in water

Z. Yang, L. Hu, T. Cao, L. An, L. Li, T. Yang and C. Zhou, New J. Chem., 2019, 43, 16441 DOI: 10.1039/C9NJ04580E

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