Rh(iii)-catalyzed highly site- and regio-selective alkenyl C–H activation/annulation of 4-amino-2-quinolones with alkynes via reversible alkyne insertion
Author:
Affiliation:
1. Department of Basic Medicinal Sciences, Graduate School of Pharmaceutical Sciences, Nagoya University, Furo-cho Chikusa, Nagoya 464-8603, Japan
Abstract
Funder
Japan Agency for Medical Research and Development
Japan Society for the Promotion of Science
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/SC/D3SC03987K
Reference57 articles.
1. A Simple and Versatile Amide Directing Group for C−H Functionalizations
2. Site-Selective C-H Bond Activation/Functionalization of Alpha-Amino Acids and Peptide-Like Derivatives
3. Transition Metal Promoted Cascade Heterocycle Synthesis through C−H Functionalization
4. Multiple Catalytic C−H Bond Functionalization for Natural Product Synthesis
5. Synthesis of Natural Products by C−H Functionalization of Heterocycless
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