Decatungstate Photocatalyzed Oxidation of Aryl Alkanols. Electron Transfer or Hydrogen Abstraction Mechanism?
Decatungstate W10O32 4- photosensitized oxidation of a series of para-X-substituted 1-aryl-1-alkanols was investigated. The only oxidation product of the side-chain of the 1-aryl-1-alkanol was the aryl ketone. The product analysis and kinetic data of the title reaction support a hydrogen atom transf...
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Published in | Organic letters Vol. 5; no. 16; pp. 2875 - 2878 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
07.08.2003
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Online Access | Get full text |
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Summary: | Decatungstate W10O32 4- photosensitized oxidation of a series of para-X-substituted 1-aryl-1-alkanols was investigated. The only oxidation product of the side-chain of the 1-aryl-1-alkanol was the aryl ketone. The product analysis and kinetic data of the title reaction support a hydrogen atom transfer mechanism in the rate-determining step. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol0349211 |