A Rapid Synthetic Approach to the ABCD Core of the Stemona Alkaloids
journal contributionposted on 18.12.2018 by Rickki L. Connelly, Jonathan P. Knowles, Kevin I. Booker-Milburn
Any type of content formally published in an academic journal, usually following a peer-review process.
A new Lewis acid-assisted Brønsted acid cascade approach for the stereoselective formation of the tetracyclic Stemona alkaloid skeleton is described in five steps from epoxide 15. Crucially, this tetracyclic product can be accessed as either C13 epimer, potentially serving as intermediates for the synthesis of a range of Stemona alkaloids.