Fragmentation of a dioxolanyl radical via nonstatistical reaction dynamics: characterization of the vinyloxy radical by ns time-resolved laser flash photolysis
Author:
Affiliation:
1. Lehrstuhl für Organische Chemie II
2. Ruhr-Universität Bochum
3. 44801 Bochum
4. Germany
5. FB 8 (Chemie-Biologie)
6. Organische Chemie I
7. Universität Siegen
8. 57068 Siegen
Abstract
Photolysis of a dioxolanyl Barton ester results in formation of the vinyloxy radical, via nonstatistical reaction dynamics. The nonstatistical reaction involves ester cleavage, CO2 loss and fragmentation of the intermediate dioxolanyl radical.
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2018/CP/C8CP03311K
Reference29 articles.
1. A comprehensive picture of the one-electron oxidation chemistry of enols, enolates and α-carbonyl radicals: oxidation potentials and characterization of radical intermediates
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3. Efficient Production of Enol Ether Radical Cations by Heterolytic Cleavage of β-Mesylate Radicals
4. Mechanistic Studies on RNA Strand Scission from a C2′-Radical
5. Direct Strand Scission in Double Stranded RNA via a C5-Pyrimidine Radical
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1. Generation and Radical–Radical Cross-Coupling of Alkenyloxy Radical;Organic Letters;2024-03-19
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