Enantioselective Synthesis of an Indenopyrrole Scaffold Containing an All-Carbon Quaternary Stereocenter via a Visible-Light-Mediated Organocatalytic Carbene Transfer Reaction
]pyrroles bearing an all-carbon quaternary stereocenter with excellent enantioselectivities by the reaction of diazo arylidene succinimides with α,β-unsaturated ketones. This work represents the first carbene transfer reaction of diazo arylidene succinimides and a cinchona alkaloid-derived catalyst in photochemical asymmetric transformation.
Authors
- Tang Yu-min
- Xing‐Peng Du
- Xin‐Ping Hui (ORCID: https://orcid.org/0000-0001-9108-7209)
- X X Li
- Peng Feng
- Hua Zhang
Institutions
- State Key Laboratory of Chemical Engineering (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-04-20
- DOI
- https://doi.org/10.1021/acs.orglett.6c01316
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Science and Technology Department of Gansu Province