Аннотация:
A series of hydroxy- and alkoxy-substituted isocoumarins were synthesized in one step by the rhodium-catalyzed C–H annulation of benzoic acids with alkynes. 8,9-Diethyl-6H-[1,3]dioxolo[4,5-f]isochromen-6-one and its isoquinolone analog have effectively inhibited the growth of six types of phytopathogenic fungi at 30 mg dm–3 concentration, the activity exceeding that of the commercial Triadimefon.
Образец цитирования:
V. B. Kharitonov, O. G. Chusova, I. O. Bekshaite, K. A. Vasiliev, A. N. Rodionov, Yu. V. Nelyubina, P. V. Dorovatovskii, D. A. Loginov, “Rhodium(III)-catalyzed C–H annulation for the construction of antifungal agents based on isocoumarin framework”, Mendeleev Commun., 35:5 (2025), 602–605