1963
DOI: 10.1002/ardp.19632960711
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Über γ‐Alkyliden‐tetronsäuren, I

Abstract: y -Alkyliden-tetronsaure-derivate kommen als Inhaltsstoffe einiger Flechtenarten vor. Ein Beispiel ist die sog. Vulpinsaure (11)2) 3), die in der Usneacee Evernia vulpina (Achatius) u. a. Flechten gefunden wird. Nahe Verwandte davon sind das Calycin4) und die P i n a~t r i n s i i u r e~) aus einigen Cetraria-und Lepraria-Arten.

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Cited by 4 publications
(2 citation statements)
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“…Their oxo-functionalized analogs, i.e., metal enolates derived from 1,3,5,7-tetracarbonyl compounds, have been studied to a much lesser extent [3][4][5][6]. The structure and properties of sodium 1,6-dioxoalka-2,4-diene-3,4-diolates formed by condensation of dialkyl oxalates with alkyl acetates or with alkyl acetates and alkyl methyl ketones were not reported previously.…”
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confidence: 99%
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“…Their oxo-functionalized analogs, i.e., metal enolates derived from 1,3,5,7-tetracarbonyl compounds, have been studied to a much lesser extent [3][4][5][6]. The structure and properties of sodium 1,6-dioxoalka-2,4-diene-3,4-diolates formed by condensation of dialkyl oxalates with alkyl acetates or with alkyl acetates and alkyl methyl ketones were not reported previously.…”
mentioning
confidence: 99%
“…), 2925 (OCH 3 , asym. ), 1650 (C 1 =O), 1610 (C 6 =O), 1526 (C=C), 1484 (δ as CH3 ), 1356 (δ s CH 3 ), 1172 (C-O). 1 H NMR spectrum, δ, ppm: 1.76 s (3H, CH 3 , A, C), 3.40 s (3H, OCH 3 , A, C), 4.88 s (1H, 2-H, A, 95%), 5.29 s (1H, 2-H, C, 5%), 5.39 s (1H, 5-H, A, C).…”
mentioning
confidence: 99%