The Infona portal uses cookies, i.e. strings of text saved by a browser on the user's device. The portal can access those files and use them to remember the user's data, such as their chosen settings (screen view, interface language, etc.), or their login data. By using the Infona portal the user accepts automatic saving and using this information for portal operation purposes. More information on the subject can be found in the Privacy Policy and Terms of Service. By closing this window the user confirms that they have read the information on cookie usage, and they accept the privacy policy and the way cookies are used by the portal. You can change the cookie settings in your browser.
1-Fluoro-1,3-enynes were stereoselectively prepared by the cross-coupling reaction of 1-alkynes with β-fluoroalkenyliodides obtained from (β-fluoroalkenyl)iodonium salts. As the reaction proceeds under mild conditions, polyfunctionalized 1-fluoro-1,3-enynes could be prepared, and the synthesis of a fluorinated analog of a natural compound was achieved using this method.
(E,E)-δ-Fluoro-α,β,γ,δ-unsaturated carbonyl compounds were stereo- and regioselectively obtained by a palladium-catalyzed Heck-type reaction of (E)-2-fluoro-1-iodo-1-alkenyliodonium salts with α,β-unsaturated carbonyl compounds. The stereoselective synthesis of the fluorinated analogue of a biologically active unsaturated fatty acid was also achieved using this reaction.
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.