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.

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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

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article

Enantioselective Synthesis of an Indenopyrrole Scaffold Containing an All-Carbon Quaternary Stereocenter via a Visible-Light-Mediated Organocatalytic Carbene Transfer Reaction

Tang Yu-min, Xing‐Peng Du, Xin‐Ping Hui, X X Li et al.
Organic Letters
Cyclopropane Reaction Mechanisms
article

Enantioselective Synthesis of an Indenopyrrole Scaffold Containing an All-Carbon Quaternary Stereocenter via a Visible-Light-Mediated Organocatalytic Carbene Transfer Reaction

Tang Yu-min, Xing‐Peng Du, Xin‐Ping Hui, X X Li, Peng Feng, Hua Zhang
article en

Abstract

]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.

Organic LettersVol. 28(17)
State Key Laboratory of Chemical Engineering (CN), Lanzhou University (CN)
National Natural Science Foundation of China, Science and Technology Department of Gansu Province
Openalex Percentile: Top 21%
Cyclopropane Reaction Mechanisms
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