Abstract:
Efficient preparative procedures for the synthesis of 2,3-disubstituted 5,6,7,8-tetraalkoxyquinolines starting from tetraalkoxybenzaldehydes are reported. The latter are available from plant (polyalkoxy)(allyl)benzenes, secondary metabolites of parsley and dill seeds.
Citation:
V. E. Kalugin, O. I. Adaeva, D. V. Demchuk, V. V. Semenov, “Synthesis of new tetraalkoxyquinolines from parsley and dill secondary metabolites”, Mendeleev Commun., 33:4 (2023), 481–483
Linking options:
https://www.mathnet.ru/eng/mendc434
https://www.mathnet.ru/eng/mendc/v33/i4/p481
This publication is cited in the following 2 articles:
Y. Zhang, J. Bai, S. Sun, “Copper(ii)-catalyzed three-component coupling sequence for the efficient synthesis of 2-arylquinolines: 1,4-dioxane serving as the C2 building block”, Mendeleev Commun., 34:3 (2024), 401–403
I. V. Smirnov, O. I. Afanasyev, K. O. Biriukov, M. I. Godovikova, D. A. Chusov, “Mn-catalyzed syngas-assisted reductive Knoevenagel condensation”, Mendeleev Commun., 34:6 (2024), 831–833
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