Abstract:
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.
Citation:
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
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https://www.mathnet.ru/eng/mendc7296
https://www.mathnet.ru/eng/mendc/v35/i5/p602
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