Why would running an aldol reaction between benzil and
Why would running an aldol reaction between benzil and dibenzyl ketone at a low temp furnish the product of a non conjugated 2,3,4,5-tetraphenylcyclopentadienone with two OHs in low yield?
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why would running an aldol reaction between benzil and dibenzyl ketone at a low temp furnish the product of a non
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