Total Synthesis of (+)-Brevianamides A and B

(+)-Brevianamides A (<b>1a</b>) and B (<b>1b</b>) are distinguished by their unique bicyclo[2.2.2]diazaoctane structure and have captured the interest of synthetic chemists due to their fascinating array of biological activities. The biosynthetic proposal of these classes of alkaloids led to the discovery of a number of interesting strategies. We present a biomimetic synthesis of these alkaloids starting from naturally occurring 4-hydroxy-l-proline and L-tryptophan. Gratifyingly, we emulate an alternative biosynthetic process through a unique elimination-isomerization sequence triggered by a dual-base system to generate the key <i>aza</i>-diene required for the Diels-Alder reaction to craft the bicyclo[2.2.2]diazaoctane structure.