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 v...

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Published inAngewandte Chemie International Edition Vol. 63; no. 51; pp. e202411709 - n/a
Main Authors Chen, Hua‐Hong, Chen, Yang‐Bo, Gao, Jun‐Zhe, Ye, Long‐Wu, Zhou, Bo
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 16.12.2024
Wiley Subscription Services, Inc
EditionInternational ed. in English
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Summary: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. A copper‐catalyzed enantioselective dehydro‐Diels–Alder reaction has been realized via vinyl cation pathway, enabling the atom‐economical synthesis of axially chiral phenyl and indolyl carbazoles. This protocol continues the first example of non‐noble metal‐catalyzed enantioselective DDA reaction. Notably, the constructed axially chiral carbazoles are applicable to asymmetric catalysis.
Bibliography:These authors contributed equally to this work.
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ISSN:1433-7851
1521-3773
1521-3773
DOI:10.1002/anie.202411709