Issue 39, 2013
From the journal:

Chemical Communications

Donor–acceptor cyclopropanes with Lawesson's and Woollins' reagents: formation of bisthiophenes and unprecedented cage-like molecules†‡

Johannes Kaschel,a   Christian D. Schmidt,a   Mark Mumby,a   Daniel Kratzert,b   Dietmar Stalkeb  and  Daniel B. Werz*a  

* Corresponding authors

a Institut für Organische und Biomolekulare Chemie der Georg-August-Universität Göttingen, Tammannstr. 2, D-37077 Göttingen, Germany
E-mail: dwerz@gwdg.de
Fax: +49 (551)399476
Tel: +49 (551)393251

b Institut für Anorganische Chemie der Georg-August-Universität Göttingen, Tammannstr. 4, D-37077 Göttingen, Germany

Abstract

Furan-derived donor–acceptor-substituted cyclopropanes were reacted with Lawesson's reagent. Depending on the reaction conditions either bisthiophenes or unprecedented cage-like molecules were obtained. Woollins' reagent always led to the respective selenium-containing cage-like compounds.

Graphical abstract: Donor–acceptor cyclopropanes with Lawesson's and Woollins' reagents: formation of bisthiophenes and unprecedented cage-like molecules

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C2CC37631H
Article type
Communication
Submitted
19 Okt 2012
Accepted
06 Dis 2012
First published
07 Dis 2012

Chem. Commun., 2013,49, 4403-4405

Permissions

Request permissions

Donor–acceptor cyclopropanes with Lawesson's and Woollins' reagents: formation of bisthiophenes and unprecedented cage-like molecules

J. Kaschel, C. D. Schmidt, M. Mumby, D. Kratzert, D. Stalke and D. B. Werz, Chem. Commun., 2013, 49, 4403 DOI: 10.1039/C2CC37631H

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