A novel method for the synthesis of α-fluoroketones via Claisen rearrangement
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.
Saved in:
Main Authors: | , , |
---|---|
其他作者: | |
格式: | Article |
出版: |
2018
|
主題: | |
在線閱讀: | https://repository.li.mahidol.ac.th/handle/123456789/9507 |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
機構: | Mahidol University |
id |
th-mahidol.9507 |
---|---|
record_format |
dspace |
spelling |
th-mahidol.95072018-02-27T11:29:59Z A novel method for the synthesis of α-fluoroketones via Claisen rearrangement Vichai Reutrakul Thongchai Kruahong Manat Pohmakotr Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics 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. 2018-02-27T04:25:24Z 2018-02-27T04:25:24Z 1994-07-04 Article Tetrahedron Letters. Vol.35, No.27 (1994), 4853-4856 10.1016/S0040-4039(00)76986-3 00404039 2-s2.0-0028302433 https://repository.li.mahidol.ac.th/handle/123456789/9507 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028302433&origin=inward |
institution |
Mahidol University |
building |
Mahidol University Library |
continent |
Asia |
country |
Thailand Thailand |
content_provider |
Mahidol University Library |
collection |
Mahidol University Institutional Repository |
topic |
Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics |
spellingShingle |
Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Vichai Reutrakul Thongchai Kruahong Manat Pohmakotr A novel method for the synthesis of α-fluoroketones via Claisen rearrangement |
description |
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. |
author2 |
Mahidol University |
author_facet |
Mahidol University Vichai Reutrakul Thongchai Kruahong Manat Pohmakotr |
format |
Article |
author |
Vichai Reutrakul Thongchai Kruahong Manat Pohmakotr |
author_sort |
Vichai Reutrakul |
title |
A novel method for the synthesis of α-fluoroketones via Claisen rearrangement |
title_short |
A novel method for the synthesis of α-fluoroketones via Claisen rearrangement |
title_full |
A novel method for the synthesis of α-fluoroketones via Claisen rearrangement |
title_fullStr |
A novel method for the synthesis of α-fluoroketones via Claisen rearrangement |
title_full_unstemmed |
A novel method for the synthesis of α-fluoroketones via Claisen rearrangement |
title_sort |
novel method for the synthesis of α-fluoroketones via claisen rearrangement |
publishDate |
2018 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/9507 |
_version_ |
1763493538353381376 |