Intermolecular α-Functionalization of Benzylamides with <i>N</i>-Nucleophiles via Oxidative Umpolung: Synthesis of Tetrasubstituted 3,3′-Oxindoles-Reference-Cited by-同舟云学术

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Intermolecular α-Functionalization of Benzylamides with N-Nucleophiles via Oxidative Umpolung: Synthesis of Tetrasubstituted 3,3′-Oxindoles

Published:2024-07-08 Issue:28 Volume:26 Page:6041-6046
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Yue¹,Yu Jiang-Ning²,Wang Yang¹^ORCID,Shi Feng¹³^ORCID

Affiliation:

1. School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China

2. School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China

3. School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02167

Reference29 articles.

1. Organocatalysis by N-Heterocyclic Carbenes

2. Recent discoveries on the structure of iodine(iii) reagents and their use in cross-nucleophile coupling

3. New Strategies for the Functionalization of Carbonyl Derivatives via α-Umpolung: From Enolates to Enolonium Ions

4. Advances in Synthetic Applications of Hypervalent Iodine Compounds

5. Chiral Hypervalent Iodines: Active Players in Asymmetric Synthesis

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