Publication:
A novel method for the synthesis of α-fluoroketones via Claisen rearrangement

1

Issued Date

1994-07-04

Resource Type

Article

ISSN

00404039

DOI

10.1016/S0040-4039(00)76986-3

Other identifier(s)

2-s2.0-0028302433

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron Letters. Vol.35, No.27 (1994), 4853-4856

Suggested Citation

Vichai Reutrakul, Thongchai Kruahong, Manat Pohmakotr A novel method for the synthesis of α-fluoroketones via Claisen rearrangement. Tetrahedron Letters. Vol.35, No.27 (1994), 4853-4856. doi:10.1016/S0040-4039(00)76986-3 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/9507

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Title

A novel method for the synthesis of α-fluoroketones via Claisen rearrangement

Author(s)

Vichai Reutrakul
 Thongchai Kruahong
 Manat Pohmakotr

Other Contributor(s)

Mahidol University

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.

Keyword(s)

Biochemistry, Genetics and Molecular Biology
 Chemistry
 Pharmacology, Toxicology and Pharmaceutics

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URI

https://repository.li.mahidol.ac.th/handle/123456789/9507

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Scopus 1991-2000