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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2023 Volume 33, Issue 4, Pages 481–483 (Mi mendc434)

This article is cited in 2 papers

Communications

Synthesis of new tetraalkoxyquinolines from parsley and dill secondary metabolites

V. E. Kalugin, O. I. Adaeva, D. V. Demchuk, V. V. Semenov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

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.

Keywords: plant allyltetraalkoxybenzenes, tetraalkoxybenzaldehydes, polyalkoxyquinoline derivatives, Knoevenagel reaction, Curtius rearrangement, Vilsmeier reaction.

Language: English

DOI: 10.1016/j.mencom.2023.06.013



© Steklov Math. Inst. of RAS, 2025