Copper‐Catalyzed Enantioselective Dehydro‐Diels–Alder Reaction: Atom‐Economical Synthesis of Axially Chiral Carbazoles
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.
Authors
- Long‐Wu Ye (ORCID: https://orcid.org/0000-0003-3108-2611)
- Yang‐Bo Chen
- Hua-Hong Chen
- Bo Zhou (ORCID: https://orcid.org/0000-0002-5551-678X)
- Jun-Zhe Gao
Institutions
- Xiamen University (CN)
- Shanghai Institute of Organic Chemistry (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2024-09-13
- DOI
- https://doi.org/10.1002/anie.202411709
- Citations
- 19
- Primary Topic
- Axial and Atropisomeric Chirality Synthesis
- Type
- article
- Field-Weighted Citation Impact
- 4.75