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https://doi.org/10.1002/cjoc.19890070309
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Cite Journal: Acta Chimica Sinica |  Publication Date: Jun 1, 1989 |
Affiliation: University of Tsukuba
The reaction of isopropenyl carbinol (2) with aqueous hydrobromic acid and hydroiodie acid gave salvilenone (1) and naphthopyranone (3) respectively. The reaction mechanism has been investigated. The formation of (3) was undergone a novel rearrangement of a tetrahydrophenalenone to a naphthopyranone.
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