trying a little experiment here...

went to a page that supplies me with a random English word

gonna put that word into the _Organic Syntheses_ search box

and see what the first hit is

all right the word is "possess"

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what have we got here...

ortho-alkylation of phenol with a terminal olefin, using dirhenium decacarbonyl as the catalyst. oh, yeah, everyone's got rhenium carbonyls lying around the stock room

ok looks like a few non-terminal alkenes worked too

catechol and hydroquinone gave mixed mono- and di-alkylation

orgsyn.org/demo.aspx?prep=v94p

in _mesitylene_ as the solvent. didn't they at least TRY to use something else? again, I complain that in older _Organic Syntheses_ entries, they'd talk about how they tried to use more commonplace solvents but failed

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