Аннотация:
An efficient method for the selective preparation of trifluoro-methyl-substituted isoindolones has been developed via RhIII catalyzed C-H activation / [4 + 1]-annulation of aryl hydroxamates with functionalized acceptor/acceptor diazo compounds as cross-coupling partners.
Образец цитирования:
D. V. Vorobyeva, A. S. Bubnova, A. G. Buyanovskaya, S. N. Osipov, “Synthesis of CF3-substituted isoindolones via rhodium(iii)-catalyzed carbenoid C–H functionalization of aryl hydroxamates”, Mendeleev Commun., 33:1 (2023), 34–36