Issue 9, 2001
From the journal:

Chemical Communications

Application of the ‘resin-capture–release’ methodology to macrocyclisation via intramolecular Suzuki–Miyaura coupling

Virginie Lobrégat,a   Gilles Alcaraz,*a   Hugues Bienayméb  and  Michel Vaultier*b  

* Corresponding authors

a S.E.S.O., UMR-CNRS 6510, Université de Rennes 1-Beaulieu, Rennes, France.
E-mail: michel.vaultier@univ-rennes1.fr

b Rhône-Poulenc Industrialisation BP 62, Saint-Fons, France.
E-mail: hugues.bienaymé@crit.rhone-poulenc.com

Abstract

Aryl boronic acids can be trapped by an ammonium hydroxide-form Dowex® Ion Exchangers resin (D-OH−) leading to polymer-ionically bound borates and cyclized, when properly designed, into macroheterocycles under Suzuki–Miyaura coupling conditions.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B101156L
Article type
Communication
Submitted
05 Feb 2001
Accepted
19 Mar 2001
First published
09 Apr 2001

Chem. Commun., 2001, 817-818

Permissions

Request permissions

Application of the ‘resin-capture–release’ methodology to macrocyclisation via intramolecular Suzuki–Miyaura coupling

V. Lobrégat, G. Alcaraz, H. Bienaymé and M. Vaultier, Chem. Commun., 2001, 817 DOI: 10.1039/B101156L

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