Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/30087
Title: Methodology for the synthesis of 4 or 5-substituted-3-perfluoroalkyl pyrazoles
Authors: Oleksik, Laurence
Award date: 2004
Presented at: University of Leicester
Abstract: Initially the perfluoroacylation of a range of commercially available vinyl ethers and conversion of the resulting perfluoroacylated enol ethers to 1-H-pyrazoles via reaction with hydrazine is reported. The selective synthesis of a range of alpha-aryl vinyl ethers using Heck chemistry is then reported. Subsequent perfluoroacylations of the vinyl ethers followed by reaction of the resulting perfluoroacyl enol ethers with hydrazine affords a range of 5-aryl-3-perfluoroalkyl pyrazoles in good yields.;Alternative methodology for the synthesis of 5-aryl-3-perfluoroalkyl pyrazoles is then described in which resin bound esters are converted to vinyl ethers <via a Tebbe reaction. Subsequent perfluoroacylations generate the expected resin bound perfluoroacyl enol ethers and cleavage with cyclisation with hydrazine liberates the desired pyrazoles in acceptable yields for this type of methodology. Finally the microwave mediated Suzuki coupling of 4-iodo-1-methyl-3-trifluoromethyl-1-H-pyrazole with various boronic acids is reported as a general way in which 4-substituted-3-perfluoroalkyl-pyrazoles can be synthesised rapidly in reasonable yields.
Links: http://hdl.handle.net/2381/30087
Type: Thesis
Level: Doctoral
Qualification: PhD
Rights: Copyright © the author. All rights reserved.
Appears in Collections:Theses, Dept. of Chemistry
Leicester Theses

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