1964
DOI: 10.1135/cccc19643115
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Imidazol-Farbstoffe XIII. Reduktion des Aroylenimidazol-Skeletts mit Lithiumaluminiumhydrid

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1965
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Cited by 6 publications
(3 citation statements)
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“…221–223°C (Lit. [ 40 ] 220–221°C); FT‐IR (KBr disk) ṽmax: 3480 (N–H), 3070 (Ar–H), 2830, 2750 (C–H), 1690 (C=O), 1640 (C=N), 1450–1620 (C=C), and 745 (C–Cl) cm −1 .…”
Section: Methodsmentioning
confidence: 99%
“…221–223°C (Lit. [ 40 ] 220–221°C); FT‐IR (KBr disk) ṽmax: 3480 (N–H), 3070 (Ar–H), 2830, 2750 (C–H), 1690 (C=O), 1640 (C=N), 1450–1620 (C=C), and 745 (C–Cl) cm −1 .…”
Section: Methodsmentioning
confidence: 99%
“…The formation of two products is possible during the reduction of compound 4a with lithium aluminum hydride [11,12,22,79,80]. Thus, only the alcohol 6 was obtained during the reaction in a mixture of ether and dioxane [11,12].…”
Section: Reactions At the Carbonyl Groupmentioning
confidence: 99%
“…The solids thus obtained are then subjected to vacuum sublimation, and the sublimate consists of practically pure dianhydride of 2,2',6,6'biphenyltetracarboxylic acid. Although a Czech patent (Arient et al, 1964) claimed that this dianhydride can be prepared by the vapor-phase oxidation of 4,5,9,10tetrahydropyrene, no physical properties were given.…”
mentioning
confidence: 99%