Issue 28, 2014

Ruthenium/Yb(OTf)3-cocatalyzed dehydrogenative synthesis of 14-substituted-14-H-dibenzo[a,j]xanthenes from β-naphthol and alcohols

Abstract

By employing [P^O]2Cl2Ru/Yb(OTf)3 as a new and efficient catalyst system [P^O = 2-(diphenylphosphino)-2,4-dimethylpentan-3-one], readily available, abundant alcohols were firstly employed for dehydrogenative synthesis of 14-substituted-14-H-dibenzo[a,j]xanthenes. Due to the inherent stability of alcohols compared to aldehydes, the presented synthetic protocol is adaptable to a broad substrate scope, there is no need for stringent protection in the whole preparation process, providing the potential to prepare products that are currently inaccessible or challenging to prepare using conventional methods. It is an important complement to the conventional synthetic methodologies.

Graphical abstract: Ruthenium/Yb(OTf)3-cocatalyzed dehydrogenative synthesis of 14-substituted-14-H-dibenzo[a,j]xanthenes from β-naphthol and alcohols

Supplementary files

Article information

Article type
Paper
Submitted
03 Jan 2014
Accepted
12 Mar 2014
First published
13 Mar 2014

RSC Adv., 2014,4, 14744-14751

Author version available

Ruthenium/Yb(OTf)3-cocatalyzed dehydrogenative synthesis of 14-substituted-14-H-dibenzo[a,j]xanthenes from β-naphthol and alcohols

X. Wang, M. Chen, F. Xie and M. Zhang, RSC Adv., 2014, 4, 14744 DOI: 10.1039/C4RA00039K

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