Development of a Late-Stage Functionalization Strategy to Access Diverse 3,5-Disubstituted 1,2,4-Thiadiazoles
Efforts to prepare amine-substituted 1,2,4-thiadiazoles typically incorporate chemical diversity in the early steps of the reaction sequence or through amine choice in coupling and aromatic substitution reactions. We developed a late-stage functionalization approach that enables facile incorporation of complex substituents and diverse nitrogen-containing functional groups at C<sub>3</sub> and C<sub>5</sub>.
Authors
- Leslie N. Aldrich (ORCID: https://orcid.org/0000-0001-8406-720X)
- Zoe A. Petros
- Philip Mickel
- Andrew Dobria (ORCID: https://orcid.org/0000-0003-4492-8022)
Institutions
- National Institutes of Health (US)
- University of Illinois Chicago (US)
- National Cancer Institute (US)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-02-16
- DOI
- https://doi.org/10.1021/acs.joc.5c02935
- Primary Topic
- Structural and Chemical Analysis of Organic and Inorganic Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00