Inhibition of Stannane-Mediated Radical Rearrangements by a Recoverable, Minimally Fluorous Selenol
Author:
Affiliation:
1. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Ilinois 60607-7061
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol990590%2B
Reference27 articles.
1. Inhibition of Rearrangements in Stannane-Mediated Radical Reduction Reactions by Catalytic Quantities of Diphenyl Diselenide. An Example of Polarity Reversal Catalysis
2. Radical Clock Reactions under Pseudo-First-Order Conditions Using Catalytic Quantities of Diphenyl Diselenide. A 77Se- and 119Sn-NMR Study of the Reaction of Tributylstannane and Diphenyl Diselenide
3. Optimizing the ratio of vinyl radical cyclizations through catalysis with diphenyl diselenide
4. Stannane-Mediated Radical Addition to Arenes. Generation of Cyclohexadienyl Radicals and Increased Propagation Efficiency in the Presence of Catalytic Benzeneselenol
5. Free Radical Chemistry of β-Lactones. Arrhenius Parameters for the Decarboxylative Cleavage and Ring Expansion of 2-Oxetanon-4-ylcarbinyl Radicals. Facilitation of Chain Propagation by Catalytic Benzeneselenol
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