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- W2950417175 abstract "Abstract On irradiation of the o -vinyl diaryl ethers 4, 7, and the D-labeled derivative 16 , a rearrangement takes place leading to the phenol 6 (from 4 ) and the corresponding vinyl-bridged hydroxy stilbenes 8/17 (from 7/16 ) as primary products. The latter compounds are further transformed into the phenanthrenes 9 and 18 after 6π-cyclization and subsequent loss of methanol and water, respectively. A mechanism involving inter- or intramolecular diradical pathways is discussed." @default.
- W2950417175 created "2019-06-27" @default.
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- W2950417175 date "2010-08-20" @default.
- W2950417175 modified "2023-09-26" @default.
- W2950417175 title "ChemInform Abstract: The Photorearrangement of o-Vinyl Diaryl Ethers into o-Hydroxy Stilbenes Evidence Against Dipolar Intermediates." @default.
- W2950417175 cites W2006376896 @default.
- W2950417175 doi "https://doi.org/10.1002/chin.199348079" @default.
- W2950417175 hasPublicationYear "2010" @default.
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