Palladium-Catalyzed Formal (3 + 2) Cycloaddition Reactions of 2-Nitro-1,3-enynes with Vinylaziridines, -epoxides, and -cyclopropanes
Author:
Affiliation:
1. School of Chemistry and Molecular Bioscience, Molecular Horizons Research Institute, University of Wollongong, Northfields Avenue, Wollongong 2522, Australia
Funder
Australian Research Council
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c01364
Reference46 articles.
1. Utilizing Palladium-Stabilized Zwitterions for the Construction of N-Heterocycles
2. Palladium-catalyzed [3 + 2] cycloaddition reaction of vinylcyclopropanes with α,β-unsaturated esters or ketones
3. Highly Diastereo- and Enantioselective Palladium-Catalyzed [3+2] Cycloaddition of Vinyl Aziridines and α,β-Unsaturated Ketones
4. Palladium-Catalyzed Regioselective [3 + 2] Cycloaddition of Vinylic Oxiranes with Activated Olefins. A Facile Synthesis of Tetrahydrofuran Derivatives
5. Pd-Catalyzed Diastereo- and Enantioselective [3+2]-Cycloaddition Reaction of Vinyl Epoxide with Nitroalkenes
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