Characterization of Reactive Intermediates Generated During Photolysis of 4-Acetoxy-4-aryl-2,5-cyclohexadienones: Oxenium Ions and Aryloxy Radicals-Reference-Cited by-同舟云学术

Characterization of Reactive Intermediates Generated During Photolysis of 4-Acetoxy-4-aryl-2,5-cyclohexadienones: Oxenium Ions and Aryloxy Radicals

Published:2008-10-31 Issue:47 Volume:130 Page:16021-16030
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wang Yue-Ting¹,Jin Kyoung Joo¹,Leopold Samuel H.¹,Wang Jin¹,Peng Huo-Lei¹,Platz Matthew S.¹,Xue Jiadan¹,Phillips David Lee¹,Glover Stephen A.¹,Novak Michael¹

Affiliation:

1. Department of Chemistry and Biochemistry, Miami University, Oxford, Ohio 45056, Department of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, Department of Chemistry, University of Hong Kong, Hong Kong, P.R. China, and School of Biological, Biomedical, and Molecular Sciences, Division of Chemistry, University of New England, Armidale, 2351, New South Wales, Australia

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja805336d

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2. Intramolecular Anodic Carbon−Carbon Bond Formation from Oxidized Phenol Intermediates. Effect of Oxygenated Substituents on the Yields of Spiro Dienones in Electrochemical and Iodobenzene Diacetate Oxidations

3. Syntheses via anodically produced phenoxenium ions. Applications in the field of peptides and carbohydrates

4. Two-electron phenolic oxidations using phenyliodonium dicarboxylates

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