Issue 2, 2010
From the journal:

Chemical Communications

Chiral bifunctional phase transfer catalysts for asymmetric fluorination of β-keto esters†‡

Xisheng Wang,a   Quan Lan,a   Seiji Shirakawaa  and  Keiji Maruoka*a  

* Corresponding authors

a Laboratory of Synthetic Organic Chemistry and Special Laboratory of Organocatalytic Chemistry, Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto, Japan
E-mail: maruoka@kuchem.kyoto-u.ac.jp
Fax: +81-75-753-4041
Tel: +81-75-753-4041

Abstract

Chiral bifunctional phase transfer catalysts introducing bis(diarylhydroxymethyl) substituents at 3,3′-positions of the chiral binaphthyl core were successfully applied to asymmetric fluorination of cyclic β-keto esters with high enantioselectivities.

Graphical abstract: Chiral bifunctional phase transfer catalysts for asymmetric fluorination of β-keto esters

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B920099A
Article type
Communication
Submitted
10 شوال 1430
Accepted
25 ذو القعدة 1430
First published
10 ذو الحجة 1430

Chem. Commun., 2010,46, 321-323

Permissions

Request permissions

Chiral bifunctional phase transfer catalysts for asymmetric fluorination of β-keto esters

X. Wang, Q. Lan, S. Shirakawa and K. Maruoka, Chem. Commun., 2010, 46, 321 DOI: 10.1039/B920099A

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