Issue 20, 2001
From the journal:

Chemical Communications

Stereoselective preparation of highly functionalized (Z)-3-magnesiated enoates by an iodine–magnesium exchange reaction

Ioannis Sapountzis,a   Wolfgang Dohlea  and  Paul Knochel*a  

* Corresponding authors

a Department Chemie, Ludwig-Maximilians-Universität München, Butenandstr. 5-13, Haus F, München, Germany.
E-mail: Paul.Knochel@cup.uni-muenchen.de;
Fax: +49-089-2180-7680;
Tel: +49-089-2180-7681

Abstract

3-Iodoenoates are converted into the corresponding alkenylmagnesium species with complete retention of configuration of the double bond; both direct reaction and copper(I)-mediated reactions with various electrophiles provide polyfunctional enoates.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B106195J
Article type
Communication
Submitted
12 Jul 2001
Accepted
05 Sep 2001
First published
27 Sep 2001

Chem. Commun., 2001, 2068-2069

Permissions

Request permissions

Stereoselective preparation of highly functionalized (Z)-3-magnesiated enoates by an iodine–magnesium exchange reaction

I. Sapountzis, W. Dohle and P. Knochel, Chem. Commun., 2001, 2068 DOI: 10.1039/B106195J

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