1965
DOI: 10.2307/1498857
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Oregon Superstitions

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Cited by 3 publications
(8 citation statements)
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“…Oakenfull, Salvesen, Jencks / Catalysis of Acetylimidazole Reactions 0.10 0.03-0.17 0 N refers to the free base form of the amine or the anion of the alcohol. 6 Ionic strength maintained at 1.0 with tetramethylammonium chloride. 6 Ionic strength maintained at 1.0 with potassium chloride.…”
Section: Resultsmentioning
confidence: 99%
“…Oakenfull, Salvesen, Jencks / Catalysis of Acetylimidazole Reactions 0.10 0.03-0.17 0 N refers to the free base form of the amine or the anion of the alcohol. 6 Ionic strength maintained at 1.0 with tetramethylammonium chloride. 6 Ionic strength maintained at 1.0 with potassium chloride.…”
Section: Resultsmentioning
confidence: 99%
“…The steady-state expression for the nucleophilic reaction of a tertiary amine with acetylimidazolium ion is given in eq 6. If kmin is the residual observed rate k /ci'fcJR.N] fc-i'[Im] + kh (6) when increasing imidazole concentration causes no further rate decrease, then knuc = kobsdkmia. A plot of l/(fcobsdkmia) against the concentration of free imidazole gives a straight line from which the ratio kjk-i' and the concentration of imidazole which gives 50% inhibition (2.2 X 10-4 Af) may be calculated.…”
Section: Mechanisms Of Reactions Of Tertiary Amines Withmentioning
confidence: 99%
“…pH 6.53 (1) Observed" with no imidazole 0.044 0.039 (2) Free TED reaction6 0.004 0.014 (3) (1) -( 2 I). 6 Calculated from the second-order rate constants for free triethylenediamine, obtained in experiments at high pH. "Obtained from the intercept at 100% triethylenediamine-H22+ concentration of (3) plotted against the percentage of fully protonated amine, calculated from the pH and pK 3.47.5 50% of maximal inhibition is approximately 2.3 X 10-4 Af (free base) in the presence of 0.4 Af triethylenediamine hydrochloride and 0.02 Af phosphate buffer, pH 6.47.…”
Section: Mechanisms Of Reactions Of Tertiary Amines Withmentioning
confidence: 99%
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