Total Synthesis of (−)-Nakadomarin A
2013-06-26T00:00:00Z (GMT) by
The convergent synthesis of the polycyclic alkaloid (−)-nakadomarin A (1) is reported. The synthesis plan identified macrocyclic lactam 4 as one of the important synthons (eight steps). The other synthon (five steps) was bicyclo[6.3.0] lactam 5 containing a single stereocenter that controlled all of the subsequent stereochemistry during the assembly process. A silyl triflate-promoted cascade of 4 and 5 was used to assemble the bulk of the alkaloid skeleton with the exception of the C5–C6 bond. The nakadomarin synthesis was then completed in one additional step.