Results 141 to 150 of about 48,544 (194)
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Agricultural and Biological Chemistry, 1979
A new synthesis of (–)-rotenone (1) has been accomplished. Decarboxylation and Vilsmeier formylation of (–)-tubaic acid (3) afforded (–)-tubaaldehyde (2) which was the key intermediate of (–)-rotenone synthesis. Condensation of 2 and Grignard reagent of phenyl 2-propynyl ether (5) and subsequent oxidation afforded (–)-1-(2,3-dihydro-4-hydroxy-2 ...
Iku Sasaki, Kyohei Yamashita
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A new synthesis of (–)-rotenone (1) has been accomplished. Decarboxylation and Vilsmeier formylation of (–)-tubaic acid (3) afforded (–)-tubaaldehyde (2) which was the key intermediate of (–)-rotenone synthesis. Condensation of 2 and Grignard reagent of phenyl 2-propynyl ether (5) and subsequent oxidation afforded (–)-1-(2,3-dihydro-4-hydroxy-2 ...
Iku Sasaki, Kyohei Yamashita
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Mechanism of the Physiological Action of Rotenone
Nature, 1960ROTENONE has been widely used as a poison for the extinction of fish populations. Its action was earlier ascribed to a histolysis of the gills1 and a blocking of the circulation2 in the gills. Recently, one of us3 has demonstrated that these effects are secondary changes due to advanced stages of poisoning.
P E, LINDAHL, K E, OBERG
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The rotenone model of Parkinson's disease
Trends in Neurosciences, 2003tetrodotoxin-insensitive [Ca]i elevations in astrocytes, subsequent a Ca2þ-dependent release of glutamate and, finally, activation of metabotropic glutamate receptors in otherastrocytes.However,wefullyagreewithAndersonand Nedergaard that there is an enormous amount of experimental and theoretical work yet to be done to characterize neurone-to-astrocyte
Céline, Perier +3 more
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ROTENONE. I. REDUCTION PRODUCTS OF ROTENONE
Journal of the American Chemical Society, 1929F. B. LaForge, L. E. Smith
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ROTENONE. IV. CONSTITUTION OF ROTENONE
Journal of the American Chemical Society, 1930openaire +1 more source
Rotenone. XXVII. Note on the Hydrogenation of Rotenone
Journal of the American Chemical Society, 1933H Haller, P Schaffer
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