Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/9507
Title: A novel method for the synthesis of α-fluoroketones via Claisen rearrangement
Authors: Vichai Reutrakul
Thongchai Kruahong
Manat Pohmakotr
Mahidol University
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 4-Jul-1994
Citation: Tetrahedron Letters. Vol.35, No.27 (1994), 4853-4856
Abstract: Fluorine-facilitated Claisen rearrangement has been employed as a key step in the synthesis of α-fluoroketones 5. The elimination of sulfenic acid from the allyl ethers 3 are effected under FVP conditions. © 1994.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028302433&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/9507
ISSN: 00404039
Appears in Collections:Scopus 1991-2000

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