B(C6F5)3-catalyzed metal-free hydrogenation of 3,6-diarylpyridazines

Wei Wang; Wei Meng; Haifeng Du

doi:10.1039/C5DT03872C

You do not have JavaScript enabled. Please enable JavaScript to access the full features of the site or access our non-JavaScript page.

B(C₆F₅)₃-catalyzed metal-free hydrogenation of 3,6-diarylpyridazines†

Wei Wang,^a Wei Meng^a and Haifeng Du*^a

Author affiliations

* Corresponding authors

^a Beijing National Laboratory of Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
E-mail: haifengdu@iccas.ac.cn
Fax: +86-10-62554449
Tel: +86-10-62652117

Abstract

This paper describes the first metal-free hydrogenation of 3,6-diarylpyridazines, which was successfully realized using B(C₆F₅)₃ as a catalyst. A variety of 1,4,5,6-tetrahydropyridazine derivatives were furnished in 85–95% yields.

This article is part of the themed collection: Main Group Transformations

Download options Please wait...

Supplementary files

Article information

DOI: https://doi.org/10.1039/C5DT03872C
Article type: Communication
Submitted: 04 Okt 2015
Accepted: 01 Des 2015
First published: 03 Des 2015

Download Citation

Dalton Trans., 2016,45, 5945-5948

Permissions

Request permissions

B(C₆F₅)₃-catalyzed metal-free hydrogenation of 3,6-diarylpyridazines

W. Wang, W. Meng and H. Du, Dalton Trans., 2016, 45, 5945 DOI: 10.1039/C5DT03872C

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.

Social activity

Fetching data from CrossRef.
This may take some time to load.

Dalton Transactions