Directing-Group-Free Palladium-Catalyzed C–H Arylation of Aldoxime Using Oxime’s Umpolung Properties
Author:
Affiliation:
1. Showa Pharmaceutical University, 3-3165 Higashi-Tamagawagakuen, Machida, Tokyo 194-8543, Japan
Funder
Showa Pharmaceutical University
Japan Science Society
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03387
Reference45 articles.
1. Zur Kenntniss der Isonitrosoverbindungen
2. Arylboronic Acid-Catalyzed C-Allylation of Unprotected Oximes: Total Synthesis of N-Me-Euphococcine
3. Nickel-catalysed asymmetric hydrogenation of oximes
4. Catalytic Reduction of Oximes to Hydroxylamines: Current Methods, Challenges and Opportunities
5. Oxime‐Derived Iminyl Radicals in Selective Processes of Hydrogen Atom Transfer and Addition to Carbon‐Carbon π‐Bonds
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