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File:2-Methylcyclohexanone to 2,2- and 2,6-dimethylcyclohexanone.png

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English: Skeletal structures for the reaction of 2-methylcyclohexanone with various bases (potassium bis(trimethylsilyl)amide (KHMDS) or potassium hydride) followed by triethylborane to form two different enolates. A subsequent reaction with iodomethane gives different methylated structural isomers depending on the enolate position.)
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Source Own work based on en:2-Methylcyclohexanone to 2,2- and 2,6-dimethylcyclohexanone.jpg created and asserted as {{PD-chem}} by en:User:EdChem, which they based on "Enoxytriethylborates and Enoxydiethylboranes" in Crich, David , ed. (2008) Reagents for Radical and Radical Ion Chemistry, Handbook of Reagents for Organic Synthesis, 11, John Wiley & Sons ISBN: 9780470065365.
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Public domain This image of a simple structural formula is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship.

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current02:04, 26 October 2020Thumbnail for version as of 02:04, 26 October 20203,263 × 1,356 (210 KB)DMacks (talk | contribs){{Information |Description={{en|en:Skeletal structures for the reaction of 2-methylcyclohexanone with various bases (en:potassium bis(trimethylsilyl)amide (KHMDS) or en:potassium hydride) followed by en:triethylborane to form two different en:enolates. A subsequent reaction with en:iodomethane gives different methylated en:structural isomers depending on the enolate position.)}} |Source={{Own}} |Date={{subst:CURRENTYEAR}}-{{subst:CURRENTMONTH}}-{{subs...

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