Talk:Penguinone
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 | This article was edited to contain a total or partial translation of Pingvinon from the Slovenian Wikipedia. Consult the history of the original page to see a list of its authors. (This notice applies to version 636152980 and subsequent versions of this page.) |
| This article was edited to contain a total or partial translation of ペンギノン from the Japanese Wikipedia. Consult the history of the original page to see a list of its authors. (This notice applies to version 636152980 and subsequent versions of this page.) |
Japanese[edit]
The last para in the Japanese article describes its reaction (or lack of) with trifluoroacetic acid, I think.
Google Translate gave me:
- Penguinone the dienone - has an annular dienone skeleton to be a substrate for phenol rearrangement, since the methyl group of the 3,5-position to inhibit the translocation of the 4-position of the methyl group, is changed to phenol can be reacted with trifluoroacetic acid there is no[japanese 1](dienone - does not cause a phenol dislocation)
However I do not know enough Japanese or organic chemistry to make sense of this, and I don't have access to the referenced German journal article. I guess it means something to do with dienone phenol rearrangement.
Si Trew (talk) 11:41, 2 December 2014 (UTC)
- ^ Hagenbruch, Bernd; Hünig, Siegfried (1983). "Ein Beitrag zur Dienon-Phenol-Umlagerung". Chemische Berichte. 116: 3884–3894. doi:10.1002/cber.19831161212.
{{cite journal}}: CS1 maint: multiple names: authors list (link)
Done[edit]
- Thanks to User:Siuenti for doing this. Si Trew (talk) 11:26, 29 December 2014 (UTC)