The Synthesis and Chemistry of 8-Substituted Bicyclo[5.1.0]oct-1(8)-ene

Article abstract of DOI:10.1002/jccs.199800060

8-Bromobicyclo[5.1.0]oct-1(8)-ene (7), an intermediate for the preparation of 8-substituted bicyclo[5.1.0]oct-1(8)-enes, was synthesized by debromination of 1,8,8-tribromobicyclo[5.1.0]octane (6). Compound 7 underwent bromo-lithium exchange followed by nucleophilic substitution reactions to generate bicyclo[5.1.0]oct-1(8)-ene (5), 8-methylbicyclo[5.1.0]oct-1(8)-ene (10), and 8-trimethylsilylbicyclo[5.1.0]oct-1(8)-ene (11). The bicyclic cyclopropenes 7, 5, 10, and 11 reacted with cyclopentadiene to form adducts 12, 13, 14, and 15, respectively. All of these Diels-Alderadducts are endo-exo isomers (endo-addition from the view of the cyclopropene and exo-addition from the view of the cyclooctene).