N-Heteropolycyclic compounds from the formal intramolecular (4 + 1)-cycloaddition of chromium aminocarbenes

Org Lett. 2013 Nov 1;15(21):5456-9. doi: 10.1021/ol4025887. Epub 2013 Oct 11.

Abstract

Chromium aminocarbenes tethered to dienes of all three electronic natures undergo an efficient intramolecular (4 + 1)-cycloaddition to give N-heteropolycyclic compounds. Ligands on chromium had a profound effect on the course of the reaction.