Regioselective pyridazine synthesis from tetrazines and alkynyl sulfides
Abstract
A regioselective synthesis of trisubstituted pyridazines from tetrazines and alkynyl sulfides is disclosed. Various pyridazines were selectively prepared by the inverse-electron-demand Diels–Alder reaction and following denitrogenation. Good transformability of sulfur-substituents allowed us to synthesize a range of pyridazines without regioisomers.