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3(2H)isoquinolones. 2. Studies on the structure and formation of aminonaphthols obtained in the preparation of 3(2H)isoquinolones

Autor: W. F. Kauanaugh, W. E. Kreighbaum, W. T. Comer

Publikováno v: Journal of Heterocyclic Chemistry. 10:317-322

The reaction of a 2-acylphenylacetic acid derivative (I) with primary amines in glacial acetic acid produces novel, colorless aminonaphthols (III) which are isomeric with the brilliant yellow 3(2H)isoquinolones (II) obtained in the same reaction. A c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d850fb60ab61d1605c88597a86fe62f6
https://doi.org/10.1002/jhet.5570100307

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Preparation of tritium-labelled phenethanolamines by catalytic reduction

Autor: H. R. Roth, W. T. Comer

Publikováno v: Journal of Labelled Compounds. 7:467-472

Tritium-labelled plenethanolamines have been readily prepared by catalytic reduction of corresponding α-aminophenones. Erythro phenethanolamine racemates are exclusively formed by Pd-catalyzed reduction of α-alkyl-α-aminophenones. In one case, an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9445ad100f75b8013119535796d69ac0
https://doi.org/10.1002/jlcr.2590070413

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Some Metabolic Effects of Substituted Alkanesulfonamidophen-ethanolamines in Rats

Autor: W. T. Comer, D. A. Riggilo, H. R. Roth

Publikováno v: Experimental Biology and Medicine. 140:667-669

SummaryThe hyperglycemic and hyperlacticacidemic effects of two isomeric series of substituted alkanesulfonamidophenethanolamines were determined in fasted rats. The metabolic responses to these agents are characteristic of β-adrenergic stimulation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::91489d9dc94be70707c701c1e4ac7ec9
https://doi.org/10.3181/00379727-140-36526

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