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.
The addition of water-resistant carbon radicals to glyoxylic oxime ether provided a new method for the one-pot synthesis of α-amino acids via a carbon-carbon bond formation. The reaction of 2-hydroxy-2-methoxyacetic acid methyl ester with benzyloxyamine and an alkyl radical gave the protected α-amino acids via the stannyl radical-mediated reaction. In the absence of Bu 3 SnH, the predominant...
Alkylative amination of aldehydes was achieved via a carbon-carbon bond formation by the intermolecular alkyl radical addition to the carbon-nitrogen double bond of oxime ethers generated in situ from aldehydes and benzyloxyamine. Alkyl radical addition to oxime ethers via a route involving the iodine atom-transfer process was found to be largely dependent on the reaction temperature and eliminated...
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.