Copper-Catalyzed Enantioselective Dehydro-Diels-Alder Reaction: Atom-Economical Synthesis of Axially Chiral Carbazoles

Angew Chem Int Ed Engl. 2024 Sep 13:e202411709. doi: 10.1002/anie.202411709. Online ahead of print.

Abstract

The dehydro-Diels-Alder (DDA) reaction is a powerful method for the construction of aromatic compounds. However, the enantioselective DDA reaction has been rarely developed, probably due to the competitive thermal reaction. Herein, we report a copper-catalyzed enantioselective DDA reaction through vinyl cation pathway. The reaction leads to the atom-economical synthesis of axially chiral phenyl and indolyl carbazoles in generally excellent yields with good to excellent atroposelectivities. This methodology represents the first example of non-noble metal-catalyzed enantioselective DDA reaction. Notably, new chiral ligand and organocatalyst derived from the constructed axially chiral carbazole are demonstrated to be useful in asymmetric catalysis.

Keywords: Asymmetric Catalysis; Axial Chirality; DDA Reaction; Heterocycles; Ynamides.