Fragment Coupling and Formation of Quaternary Carbons by Visible-Light Photoredox Catalyzed Reaction of tert -Alkyl Hemioxalate Salts and Michael Acceptors
Author:
Affiliation:
1. Department of Chemistry; University of California; Irvine California 92697-2025 United States
Publisher
John Wiley & Sons, Inc.
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/0471264229.os094.13/fullpdf
Reference18 articles.
1. Department of Chemistry, University of California, Irvine, California 92697−2025 leoverma@uci.edu
2. Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling
3. Formation of quaternary carbon centres from tertiary alcohols by free radical methods
4. The invention of new radical chain reactions. Part 9. Further radical chemistry of thiohydroxamic esters; formation of carbon–carbon bonds
5. Direct Construction of Quaternary Carbons from Tertiary Alcohols via Photoredox-Catalyzed Fragmentation of tert-Alkyl N-Phthalimidoyl Oxalates
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1. Interrupting the Barton–McCombie Reaction: Aqueous Deoxygenative Trifluoromethylation of O-Alkyl Thiocarbonates;Organic Letters;2021-01-14
2. Tertiary Alcohols as Radical Precursors for the Introduction of Tertiary Substituents into Heteroarenes;ACS Catalysis;2019-03-19
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