2005
DOI: 10.1007/s11171-005-0040-6
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Synthesis of Analogues of Natural Coumarins and Coumarinolignans

Abstract: 3-Aryl-4H-coumarins with the 1,3-benzodioxol, 1,4-benzodioxane, and 1,5-benzodioxepane moieties were synthesized by modified methods. The English version of the paper: Russian Journal of Bioorganic Chemistry, 2005, vol. 31, no. 3; see also http://www.maik.ru.

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Cited by 2 publications
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“…According to method A, the appropriate salicylal dehyde (I)-(IV) phenoxyacetic acid (V) was con densed in the Perkin reaction [1]. In method B, start ing compounds were condensed in dimethylforma mide in the presence of trichloroacetic acid and acetic anhydride according to the Edgeworin synthesis pro cedure [3].…”
Section: Methodsmentioning
confidence: 99%
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“…According to method A, the appropriate salicylal dehyde (I)-(IV) phenoxyacetic acid (V) was con densed in the Perkin reaction [1]. In method B, start ing compounds were condensed in dimethylforma mide in the presence of trichloroacetic acid and acetic anhydride according to the Edgeworin synthesis pro cedure [3].…”
Section: Methodsmentioning
confidence: 99%
“…
Natural coumarin and phenoxycoumarin bioregu lators have a broad range of physiological activity and are a fertile field for chemical modifications [1].Traditionally, substituted and unsubstituted 3 phe noxycoumarins are synthesized using the Perkin reac tion [2], the Edgeworin synthesis procedure [3], the Kostanetsky-Robinson reaction, or modified versions of them [4].The most common method used to synthesize phe noxycoumarins containing O aryl substituents in the 3 position is the interaction of the appropriate alde hydes with phenoxyacetic acids and their functional derivatives. Compounds possessing antimicrobial [2], herbicidal, fungicidal, and insecticidal activity, as well as activity against dermatophytes [5], were identified during the study of biological activity.

Abstract-The synthesis of substituted and unsubstituted 3 phenoxycoumarins is described.

…”
mentioning
confidence: 99%
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