Chiral ruthenium porphyrin-catalyzed asymmetric cyclopropanation of 1,3-dienes with <i>tert</i>-butyl 2-cyano-2-diazoacetate as the carbene source

With the chiral ruthenium porphyrin complex ( S , R )-cmcpor-RuCO as a catalyst and tert -butyl 2-cyano-2-diazoacetate as the carbene source, a panel of substituted vinylcyclopropanes is readily prepared in good product yields and high enantioselectivity.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-11-28
DOI
https://doi.org/10.1039/d4qo01576b
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.50

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article

Chiral ruthenium porphyrin-catalyzed asymmetric cyclopropanation of 1,3-dienes with tert-butyl 2-cyano-2-diazoacetate as the carbene source

Chi‐Ming Che, Yungen Liu, Siqi Zhong, Hao‐Chong Tan et al.
2 citations
Organic Chemistry Frontiers
Cyclopropane Reaction Mechanisms
0.50
article

Chiral ruthenium porphyrin-catalyzed asymmetric cyclopropanation of 1,3-dienes with tert-butyl 2-cyano-2-diazoacetate as the carbene source

Chi‐Ming Che, Yungen Liu, Siqi Zhong, Hao‐Chong Tan, Huahua Wang
article en
2 citations

Abstract

With the chiral ruthenium porphyrin complex ( S , R )-cmcpor-RuCO as a catalyst and tert -butyl 2-cyano-2-diazoacetate as the carbene source, a panel of substituted vinylcyclopropanes is readily prepared in good product yields and high enantioselectivity.

Organic Chemistry FrontiersVol. 12(2)
Southern University of Science and Technology (CN), State Key Laboratory of Synthetic Chemistry (CN), University of Hong Kong (HK)
National Natural Science Foundation of China, Innovation and Technology Commission, Southern University of Science and Technology
Openalex Percentile: Top 37%
Cyclopropane Reaction Mechanisms
0.50
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