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?
Why would running an aldol reaction between benzil
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?