posted on 2018-11-27, 17:33authored byBoubacar Baldé, Guillaume Force, Lucile Marin, Régis Guillot, Emmanuelle Schulz, Vincent Gandon, David Lebœuf
A new
and efficient reaction sequence between 2-furylcarbinols,
anilines, and α-haloamides has been developed to afford highly
functionalized cyclopenta[b]piperazinones. This transformation
was accomplished through an aza-Piancatelli cyclization/azaoxyallyl
cation trapping with a complete control of the diastereoselectivity.