Photochemical Lumiketone-Type Rearrangement of 3-Methoxyphenol Promoted by AlBr3
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/64/11/64_11_3468/_pdf
Reference12 articles.
1. Photoisomerizations of protonated phenols. Extension of the photochemistry of cyclohexa-2,5-dienones
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3. The use of homogeneous and heterogeneous Lewis acids to catalyse the photoisomerizations of phenols
4. A quantitative examination of the photoisomerization of some protonated phenols
5. Novel photocycloaddition of 2-naphthols to ethylene in the presence of Lewis acid
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1. Photochemical rearrangement reactions of bicyclic molecules that contain a cyclopropane ring;New Journal of Chemistry;2018
2. Photochemistry of Aromatic Compounds;Lecture Notes in Chemistry;2016-11-19
3. ChemInform Abstract: Photochemical Lumiketone-Type Rearrangement of 3-Methoxyphenol Promoted by AlBr3.;ChemInform;2010-08-22
4. Photochemistry of Phenols;PATAI'S Chemistry of Functional Groups;2009-12-15
5. Thermal and Photochemical Rearrangement of Bicyclo[3.1.0]hex-3-en-2-one to the Ketonic Tautomer of Phenol. Computational Evidence for the Formation of a Diradical Rather than a Zwitterionic Intermediate;Journal of the American Chemical Society;2002-11-26
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