| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1314798 | Journal of Fluorine Chemistry | 2007 | 5 Pages |
Abstract
Selective mono-fluorination of 1,2- and 1,3-diols was achieved using N,N-diethyl-4-methoxybenzamide diethyl acetal and Et3N-3HF. The reaction proceeds through a cyclic acetal of the benzamide, and only one hydroxy group was fluorinated and another one was acylated.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Mitsuhiro Suwada, Tsuyoshi Fukuhara, Shoji Hara,