Issue 2, 2018

Thiazolium salt-catalyzed C–C triple bond cleavage for accessing substituted 1-naphthols via benzannulation

Abstract

The first thiazolium salt-catalyzed C–C triple bond cleavage of benzene-linked allene-ynes has been established. The reaction pathway involves [2+2] cycloaddition and ring-opening of in situ generated cyclobutenes with H2O under mild and convenient conditions, and provides practical access to substituted 1-naphthols with potentially valuable applications.

Graphical abstract: Thiazolium salt-catalyzed C–C triple bond cleavage for accessing substituted 1-naphthols via benzannulation

Supplementary files

Article information

Article type
Communication
Submitted
15 Nov 2017
Accepted
29 Nov 2017
First published
30 Nov 2017

Chem. Commun., 2018,54, 164-167

Thiazolium salt-catalyzed C–C triple bond cleavage for accessing substituted 1-naphthols via benzannulation

P. Zhou, J. Wang, T. Zhang, G. Li, W. Hao, S. Tu and B. Jiang, Chem. Commun., 2018, 54, 164 DOI: 10.1039/C7CC08792F

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