Asymmetric Redox Allylic Alkylation to Access 3,3′‐Disubstituted Oxindoles Enabled by Ni/NHC Cooperative Catalysis-Reference-Cited by-同舟云学术

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Asymmetric Redox Allylic Alkylation to Access 3,3′‐Disubstituted Oxindoles Enabled by Ni/NHC Cooperative Catalysis

Published:2022-03-29 Issue:22 Volume:61 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew Chem Int Ed

Author:

Fan Tao¹,Song Jin²,Gong Liu‐Zhu¹³^ORCID

Affiliation:

1. Department of Chemistry University of Science and Technology of China Hefei 230026 China

2. Institutes of Physical Science and Information Technology Anhui University Hefei 230601 China

3. Center for Excellence in Molecular Synthesis of Chinese Academy of Sciences Hefei 230026 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202201678

Reference132 articles.

1. For selected recent reviews see:

2. Acyl anion free N-heterocyclic carbene organocatalysis

3. On the Mechanism of N-Heterocyclic Carbene-Catalyzed Reactions Involving Acyl Azoliums

4. Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes

5. Recent advances in employing homoenolates generated by N-heterocyclic carbene (NHC) catalysis in carbon–carbon bond-forming reactions

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