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.

Supplementary files

Article information

Article type
Research Article
Submitted
12 Jul 2024
Accepted
26 Aug 2024
First published
29 Aug 2024
This article is Open Access
Creative Commons BY-NC license

Org. Chem. Front., 2024, Accepted Manuscript

Regioselective pyridazine synthesis from tetrazines and alkynyl sulfides

C. Yamamoto, K. Numata, M. Suzuki and S. Yoshida, Org. Chem. Front., 2024, Accepted Manuscript , DOI: 10.1039/D4QO01286K

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