Using Ring Strain to Control 4π-Electrocyclization Reactions: Torquoselectivity in Ring Closing of Medium-Ring Dienes and Ring Opening of Bicyclic Cyclobutenes

Syntheses of strained cyclic dienes were accomplished via palladium­(II)-catalyzed oxidative cyclizations of terminal bis­(vinylboronate esters). The reactions generate strained (<i>E</i>,<i>E</i>)-1,3-dienes that undergo spontaneous 4π-electrocyclizations to form bicyclic cyclobutenes. Formation of the cyclobutenes is driven by the strain in the medium-ring (<i>E,E</i>)-1,3-diene intermediate. Thermal ring openings of the cyclobutenes give (<i>Z</i>,<i>Z</i>)-1,3-diene products, again for thermodynamic reasons. DFT calculations verified the thermodynamic versus kinetic control of the reactions, and kinetic studies are in excellent agreement with the calculated energy changes. An extension of the tandem coupling/4π-electrocyclization pathway was demonstrated by a palladium­(II)-catalyzed oxidative homocoupling/8π-electrocyclization cascade