Catalytic Asymmetric Metallocyclopropanation Reactions Using Chloroform as a Carbyne Equivalent

-aryl substituent of the ligand. Application in the parallel synthesis of enantioenriched 1,2-diarylcyclopropanes bearing pharmaceutically relevant heterocycles is demonstrated.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-07-26
DOI
https://doi.org/10.1021/jacs.6c05240
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

Catalytic Asymmetric Metallocyclopropanation Reactions Using Chloroform as a Carbyne Equivalent

Eric A. Voight, Jonathon M. Young, Alexander J. Rago, Martin Garcia Chavez et al.
Journal of the American Chemical Society
Cyclopropane Reaction Mechanisms
article

Catalytic Asymmetric Metallocyclopropanation Reactions Using Chloroform as a Carbyne Equivalent

Eric A. Voight, Jonathon M. Young, Alexander J. Rago, Martin Garcia Chavez, Christopher Uyeda, Raymond Martinez, Divya Garg, Luke R. Harrison
article en

Abstract

-aryl substituent of the ligand. Application in the parallel synthesis of enantioenriched 1,2-diarylcyclopropanes bearing pharmaceutically relevant heterocycles is demonstrated.

Journal of the American Chemical Society
Purdue University West Lafayette (US), AbbVie (United States) (US), Applied Technologies (United States) (US)
Openalex Percentile: Top 16%
Cyclopropane Reaction Mechanisms
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