Hume 1966
DOI: 10.1007/978-1-349-15271-1_18
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Hume’s Account of Obligation

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Cited by 2 publications
(3 citation statements)
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“…Marks and co-workers reported the use of 4,4-diphthalimidobenzil as a starting dicarbonyl compound. 12 The condensation product bearing protected amino groups was deprotected by hydrazinolysis to afford the target chromophore. Since the use of bulky phthaloyl group for protecting amino group could result in poor solubility of the substrates and harsh reaction conditions for hydrazinolysis, the chromophores were produced in poor overall yield.…”
Section: Resultsmentioning
confidence: 99%
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“…Marks and co-workers reported the use of 4,4-diphthalimidobenzil as a starting dicarbonyl compound. 12 The condensation product bearing protected amino groups was deprotected by hydrazinolysis to afford the target chromophore. Since the use of bulky phthaloyl group for protecting amino group could result in poor solubility of the substrates and harsh reaction conditions for hydrazinolysis, the chromophores were produced in poor overall yield.…”
Section: Resultsmentioning
confidence: 99%
“…Table 1. Characterization results for 2-(4-nitrophenyl)-4,5-di(aminophenyl)imidazole (I) also are listed in Table 1 for comparison 12 . It is found that all the four chromophores show larger µ g β 0 value than that of I, which is attributed to the positive contribution of their elongated conjugation lengths.…”
Section: Resultsmentioning
confidence: 99%
“…Previously, in a preparation of a lophin-type compounds, Marks and co-workers reported the use of 4,4'-diphthalimidobenzil as a starting dicarbonyl compound. 10 The condensation product was further hydrazinolysed to afford the target diamino product. Since the use of the bulky phthaloyl group as a protecting amino group could result in poor solubility of the substrates and due to the harsh reaction conditions for hydrazinolysis, the chromophores were produced in poor overall yield.…”
mentioning
confidence: 99%