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.
Starting with a variety of non-functionalized carbon skeletons and employing various combinations of five key transformations provides an easy access to most of the naturally occurring Annonaceous acetogenins. A particular emphasis is given to the dominant structural feature that appears in more than 40% of the known acetogenins. This is a linear, ten-carbon skeleton comprising two adjacent tetrahydrofurane...
An efficient synthesis of (+)-disparlure has been achieved in > 99.8% ee via the Sharpless asymmetric dihydroxylation followed by Mitsunobu inversion of one hydroxyl group and conversion of the resultant erythro diol to the cis epoxide.
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.