Issue 29, 2006
From the journal:

Chemical Communications

Monofluorinated di- and tetrahydropyrans via Prins-type cyclisations

Adrian P. Dobbs,*a   Levan Pivnevi,b   Mark J. Penny,a   Săsa Martinović,c   James N. Ileyb  and  Peter T. Stephensond  

* Corresponding authors

a Department of Chemistry, Queen Mary, University of London, Mile End Road, London, UK
E-mail: A.Dobbs@qmul.ac.uk

b Department of Chemistry, The Open University, Walton Hall, Milton Keynes, UK

c Department of Chemistry, University of Exeter, Stocker Road, Exeter, UK

d Discovery Chemistry, Pfizer Global R&D, Sandwich, Kent, UK

Abstract

The synthesis of a range of fluorinated heterocycles is described via a Lewis acid-mediated Prins-type cyclisation.

Graphical abstract: Monofluorinated di- and tetrahydropyrans via Prins-type cyclisations

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B606121D
Article type
Communication
Submitted
02 May 2006
Accepted
26 May 2006
First published
14 Jun 2006

Chem. Commun., 2006, 3134-3136

Permissions

Request permissions

Monofluorinated di- and tetrahydropyrans via Prins-type cyclisations

A. P. Dobbs, L. Pivnevi, M. J. Penny, S. Martinović, J. N. Iley and P. T. Stephenson, Chem. Commun., 2006, 3134 DOI: 10.1039/B606121D

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