Preparation of 2-Trialkylsiloxy- Substituted 1,3-Dienes and Their Diels−Alder/Cross-Coupling Reactions

2-Triethylsiloxy-substituted 1,3-butadiene has been prepared in gram quantities from chloroprene via a simple synthetic procedure. Silatrane
and catechol-substituted analogues of this main group element substituted diene were prepared by ligand exchange and characterized by
X-ray crystallography in addition to standard spectroscopic techniques. Diels−Alder reactions of these dienes are reported as well as subsequent
TBAF assisted/Pd-catalyzed Hiyama cross-coupling reactions of those Diels−Alder adducts.