Abstract
AbstractSelectivity between the two double bonds of the title compound (I) for a number of reagents is observed: cycloaddition of cyclopentadiene (II) or anthracene as well as the reduction with molecular hydrogen takes place at the unsubstituted double bond, whereas the product (V) of a reduction at the more substituted double bond is obtained when (I) is treated with PhSH or 1,3‐cyclohexadiene (or α‐terpinene).
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