Abstract
The hexadehydro-Diels-Alder (HDDA) reactions between suitably substituted 1,3-diynes and alkynes produce highly reactive benzynes under thermal conditions without catalysts. DFT calculations and distortion/interaction analyses show that, for the activated substrates, the stepwise diradical pathway is more favorable than the concerted [4 + 2] process. One manifestation of this mechanism is that alkynyl substituents dramatically accelerate HDDA reactions, mainly by decreasing the distortion energy required to achieve the diradical transition state.
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