Issue 45, 2015
From the journal:

RSC Advances

N-heterocyclic carbene-catalysed pentafluorophenylation of aldehydes†

Guang-Fen Du,ab   Fen Xing,b   Cheng-Zhi Gu,*b   Bin Dai*b  and  Lin Heb  

* Corresponding authors

a School of Chemical Engineering and Technology, Tianjin University. Tianjin 300072, China

b School of Chemistry and Chemical Engineering, Shihezi University, Xinjiang Uygur Autonomous Region, China
E-mail: gcz_tea@shzu.edu.cn, db_tea@shzu.edu.cn
Fax: +86-993-2057270

Abstract

N-heterocyclic carbenes have been utilized as highly efficient organocatalysts to catalyse multifluorophenylation of aldehydes with pentafluorophenyltrimethylsilane or bis(trimethylsilyl)tetrafluorobenzene to afford the corresponding fluorinated adducts in 49–99% yields.

Graphical abstract: N-heterocyclic carbene-catalysed pentafluorophenylation of aldehydes

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C5RA05487G
Article type
Communication
Submitted
27 Mär 2015
Accepted
13 Apr 2015
First published
13 Apr 2015

RSC Adv., 2015,5, 35513-35517

Author version available

Download author version (PDF)

Permissions

Request permissions

N-heterocyclic carbene-catalysed pentafluorophenylation of aldehydes

G. Du, F. Xing, C. Gu, B. Dai and L. He, RSC Adv., 2015, 5, 35513 DOI: 10.1039/C5RA05487G

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