Demonstrates the transformation of imines into nitriles, indicating versatile synthesis methods.
Herein, we report the selective transformation of N‑(4H‑1,2,4‑triazol‑4‑yl)imines into substituted benzonitriles. These imines are readily accessible from aldehydes. The method provides a rapid and mild procedure that utilizes a previously undescribed nitrogen source. This transformation offers excellent selectivity and facile product isolation. A series of aromatic nitriles bearing various functional groups were obtained in high yields (up to 98%).
No takes yet. Share an insight, caveat, or question.
Beletskii et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: