2026-10-13T09:08:14Z https://api.figshare.com/v2/oai

oai:figshare.com:article/33959504 2026-09-21T18:11:20Z category_4 category_8 category_14 category_15 category_21 category_24 category_272 category_873 category_734 category_106 portal_63 item_type_3 month_year_09_2026

Heptafluorobutyric Acid-Induced Cross-Dehydrogenative Coupling Reactions of 1,2,4-Triazines. Part 2: p‑Coupling with Arylamines Anastasia P. Potapova (25085183) Elisaveta M. Gurina (25085186) Igor A. Khalymbadzha (1933894) Anton N. Tsmokaluk (17629644) Ainur D. Sharapov (25085189) Vasiliy S. Gaviko (25085192) Alexander S. Novikov (1616380) Dmitry S. Kopchuk (9406253) Ramil F. Fatykhov (25085195) Biochemistry Microbiology Molecular Biology Neuroscience Biotechnology Evolutionary Biology Environmental Sciences not elsewhere classified Chemical Sciences not elsewhere classified Biological Sciences not elsewhere classified Science Policy p ‑ coupling known fluorophore scaffolds dehydrogenative coupling reactions dehydrogenative coupling reaction easily accessible 1 mild conditions material design induced cross heptafluorobutyric acid drug development A heptafluorobutyric acid-induced cross-dehydrogenative coupling reaction of arylamines with 1,2,4-triazines has been described. This metal-free protocol enables regioselective para-C–H hetarylation of diverse arylamines including well-known fluorophore scaffolds, such as triphenylamine, carbazole, and phenothiazine, with easily accessible 1,2,4-triazines under mild conditions. This approach has potential for drug development and material design. 2026-09-21T00:00:00Z Dataset Dataset 10.1021/acs.joc.6c00932.s001 https://figshare.com/articles/dataset/Heptafluorobutyric_Acid-Induced_Cross-Dehydrogenative_Coupling_Reactions_of_1_2_4-Triazines_Part_2_p_Coupling_with_Arylamines/33959504 CC BY-NC 4.0