Monofluorinated di- and tetrahydropyrans via Prins-type cyclisations

Journal article

Peer reviewed

Adrian P Dobbs, Levan Pivnevi, Mark J Penny, Săsa Martinović, James N Iley and Peter T Stephenson

Chemical communications (Cambridge, England), (29), pp.3134-3136

01/01/2006

PMID: 16855710

Abstract

Acids - chemistry

Cyclization

Fluorine - chemistry

Fluorine Compounds - chemical synthesis

Fluorine Compounds - chemistry

Pyrans - chemical synthesis

Pyrans - chemistry

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

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Title: Monofluorinated di- and tetrahydropyrans via Prins-type cyclisations
Creators: Adrian P Dobbs - Queen Mary University of London
Levan Pivnevi - The Open University
Mark J Penny - Queen Mary University of London
Săsa Martinović
James N Iley
Peter T Stephenson - Pfizer
Publication Details: Chemical communications (Cambridge, England), (29), pp.3134-3136
Publication Date: 01/01/2006
Identifiers: 99959874002346; WOS:000239137500026
Academic Unit: School of Chemistry and Chemical Engineering; Department of Chemistry
Language: English
Resource Type: Journal article