Fluorinated (hetero)cycles via ring-closing metathesis of fluoride- and trifluoromethyl-functionalized olefins

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Publication year
2004Source
Tetrahedron Letters, 45, 5, (2004), pp. 959-963ISSN
Publication type
Article / Letter to editor

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Organization
Synthetic Organic Chemistry
Solid State Chemistry
Journal title
Tetrahedron Letters
Volume
vol. 45
Issue
iss. 5
Page start
p. 959
Page end
p. 963
Subject
Molecular Materials; Synthetic Organic ChemistryAbstract
Ring-closing metathesis(RCM) has been shown to be a viable tool to incorporate fluoride and trifluoromethyl substituents in (hetero)cyclic ring systems. 2-Fluoroacrylamides were cyclized to the corresponding lactams, and trifluoromethyl- substituted olefins were cyclized to yield trifluoromethylated cyclopentenes, pyrrolines and a dihydrofuran derivative. (C) 2003 Elsevier Ltd. All rights reserved.
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